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 S L V E Q R P R W V L V A R G Q A E T
AAEX02035468, TRBV1*01 , F GCA AGC CTG GTG GAG CAA AGG CCC CGC TGG GTC CTG GTA GCT CGT GGG CAG GCT GAA ACC
___________________CDR1-IMGT____________________
21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
L H C I L R D S Q Y P W M S
AAEX02035468, TRBV1*01 , F CTG CAC TGC ATC CTG AGA GAT TCC CAG ... ... ... ... ... ... TAC CCT TGG ATG AGC
_______________CDR2-
41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
W Y Q Q D L Q G Q L Q V L A T L R S
AAEX02035468, TRBV1*01 , F TGG TAC CAA CAG GAT CTC CAG GGG CAA CTG CAG GTG CTG GCC ACT CTG CGG AGC ... ...
IMGT________________
61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80
P G D E E L V S R P G A D Y R V T
AAEX02035468, TRBV1*01 , F ... ... CCC GGG GAC GAG GAG CTC GTA TCC CGT CCT ... GGA GCA GAT TAC CGG GTC ACG
81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100
R V N S T E L R L H V A N V T Q S R T L
AAEX02035468, TRBV1*01 , F AGG GTC AAC AGC ACG GAG CTG AGG CTG CAC GTG GCC AAT GTG ACC CAG AGC AGA ACC CTG
_CDR3-IMGT_
101 102 103 104 105 106
Y C T C S K
AAEX02035468, TRBV1*01 , F TAC TGC ACC TGC AGT AAA GA