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
G A L V S Q K P R R D I C Q R G T S I T
AAEX02035465, TRBV29*01 , F GGA GCT CTT GTC TCT CAA AAG CCG CGC AGG GAC ATC TGT CAA CGT GGG ACC TCC ATT ACC
___________________CDR1-IMGT____________________
21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
I H C E V D T Q V T L M F
AAEX02035465, TRBV29*01 , F ATC CAC TGT GAG GTC GAT ACC CAA GTC ... ... ... ... ... ... ... ACC TTG ATG TTC
_______________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 L P G Q S L I L I A T A N Q G
AAEX02035465, TRBV29*01 , F TGG TAC CGT CAG CTC CCA GGA CAG AGC TTG ATA CTG ATT GCA ACC GCA AAC CAG GGT ...
IMGT________________
61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80
A E A T Y E S G F T R E K F P I S R
AAEX02035465, TRBV29*01 , F ... ... GCA GAG GCC ACC TAC GAA AGT GGA TTT ACC AGG GAG AAG TTT CCC ATC AGC CGC
81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100
R T L M F S T L T V S N L S L E D T S
AAEX02035465, TRBV29*01 , F CGA ACC CTA ATG TTC TCC ACT CTG ACT GTG AGC AAC CTG AGC CTC GAA GAC ACC AGC
___CDR3-IMGT___
101 102 103 104 105 106 107
S Y F C S A R
AAEX02035465, TRBV29*01 , F TCT TAC TTC TGC AGC GCT AGA GA