When several alleles are shown, the nucleotide mutations and amino acid
changes for a given codon are indicated in red letters. These polymorphic mutations are reported in
Tables of alleles.
Dashes indicate identical nucleotides. Dots indicate gaps according to the
IMGT unique numbering.
Blanks indicate partial sequences (blanks at the 5' and/or 3' end).
N (Asn, asparagine) of potential N-glycosylation sites (NXS/T, where X is different from P), (N-linked glycosylation) is shown is green (site is underlined in CH-S and in pages edited before 14/10/2009).
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
A Q T I H Q R P L A R V Q L V G S L L S
AAEX02035465, TRBV30*01 , F GCT CAG ACT ATC CAC CAA AGG CCG CTT GCC AGG GTG CAG CTT GTG GGC AGC CTG CTC TCC
___________________CDR1-IMGT____________________
21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
L E C T V Q G A S S P Y L Y
AAEX02035465, TRBV30*01 , F CTG GAA TGT ACC GTG CAG GGG GCA TCG ... ... ... ... ... ... AGC CCT TAT CTC TAC
_______________CDR2-
41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
W Y R Q S L G G A P Q L L F S S L S
AAEX02035465, TRBV30*01 , F TGG TAC CGG CAG TCC CTG GGA GGT GCG CCC CAG CTA CTC TTC TCC TCA TTA AGT ... ...
IMGT________________
61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80
V T Q I V P E T P H N F T A S R
AAEX02035465, TRBV30*01 , F ... ... ... GTT ACC CAG ATA GTC CCT GAG ACA CCG ... CAC AAC TTC ACA GCC TCC AGG
81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100
P Q N G Q F I L S S K K L L L S D S G
AAEX02035465, TRBV30*01 , F CCC ... CAG AAC GGC CAG TTC ATC CTG AGT TCT AAG AAG CTC CTT CTC AGT GAC TCT GGC
___CDR3-IMGT___
101 102 103 104 105 106 107
F Y L C A W S
AAEX02035465, TRBV30*01 , F TTC TAC CTC TGC GCC TGG AGT CT