Canonical Allele Identifier: CA2677957699
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356757_31356758insCCT , CM000668.2:g.31356757_31356758insCCT GRCh38
NC_000006.11:g.31324534_31324535insCCT , CM000668.1:g.31324534_31324535insCCT GRCh37
NC_000006.10:g.31432513_31432514insCCT NCBI36
NG_023187.1:g.5456_5457insGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1747_1748insGGA
ENST00000481849.6:n.1747_1748insGGA
ENST00000497377.6:n.1747_1748insGGA
ENST00000640094.2:c.274_275insGGA ENSP00000491275.2:p.Tyr91_Lys92insArg
ENST00000696558.1:c.274_275insGGA ENSP00000512716.1:p.Tyr91_Lys92insArg
ENST00000696559.1:c.274_275insGGA ENSP00000512717.1:p.Tyr91_Lys92insArg
ENST00000696560.1:c.274_275insGGA ENSP00000512718.1:p.Tyr91_Lys92insArg
ENST00000696561.1:c.274_275insGGA ENSP00000512719.1:p.Tyr91_Lys92insArg
ENST00000696562.1:c.274_275insGGA ENSP00000512720.1:p.Tyr91_Lys92insArg
ENST00000412585.7:c.274_275insGGA MANE Select ENSP00000399168.2:p.Tyr91_Lys92insArg
ENST00000412585.6:c.274_275insGGA ENSP00000399168.2:p.Tyr91_Lys92insArg
ENST00000434333.1:c.307_308insGGA ENSP00000405931.1:p.Tyr102_Lys103insArg
ENST00000474381.1:n.149_150insGGA
ENST00000498007.1:n.295_296insGGA
ENST00000603274.1:n.111_112insCCT
NM_005514.6:c.274_275insGGA NP_005505.2:p.Tyr91_Lys92insArg
XM_011514556.1:c.307_308insGGA XP_011512858.1:p.Tyr102_Lys103insArg
XM_011514557.1:c.274_275insGGA XP_011512859.1:p.Tyr91_Lys92insArg
XR_926175.1:n.284_285insGGA
NM_005514.7:c.274_275insGGA NP_005505.2:p.Tyr91_Lys92insArg
NM_005514.8:c.274_275insGGA MANE Select NP_005505.2:p.Tyr91_Lys92insArg