Canonical Allele Identifier: CA2677957612
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356711_31356712insGT , CM000668.2:g.31356711_31356712insGT GRCh38
NC_000006.11:g.31324488_31324489insGT , CM000668.1:g.31324488_31324489insGT GRCh37
NC_000006.10:g.31432467_31432468insGT NCBI36
NG_023187.1:g.5501_5502insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1792_1793insAC
ENST00000481849.6:n.1792_1793insAC
ENST00000497377.6:n.1792_1793insAC
ENST00000640094.2:c.319_320insAC ENSP00000491275.2:p.Gly107AspfsTer?
ENST00000696558.1:c.319_320insAC ENSP00000512716.1:p.Gly107AspfsTer?
ENST00000696559.1:c.319_320insAC ENSP00000512717.1:p.Gly107AspfsTer?
ENST00000696560.1:c.319_320insAC ENSP00000512718.1:p.Gly107AspfsTer?
ENST00000696561.1:c.319_320insAC ENSP00000512719.1:p.Gly107AspfsTer?
ENST00000696562.1:c.319_320insAC ENSP00000512720.1:p.Gly107AspfsTer?
ENST00000412585.7:c.319_320insAC MANE Select ENSP00000399168.2:p.Gly107AspfsTer?
ENST00000412585.6:c.319_320insAC ENSP00000399168.2:p.Gly107AspfsTer?
ENST00000434333.1:c.352_353insAC ENSP00000405931.1:p.Gly118AspfsTer?
ENST00000474381.1:n.194_195insAC
ENST00000498007.1:n.340_341insAC
ENST00000603274.1:n.65_66insGT
NM_005514.6:c.319_320insAC NP_005505.2:p.Gly107AspfsTer?
XM_011514556.1:c.352_353insAC XP_011512858.1:p.Gly118AspfsTer?
XM_011514557.1:c.319_320insAC XP_011512859.1:p.Gly107AspfsTer?
XR_926175.1:n.329_330insAC
NM_005514.7:c.319_320insAC NP_005505.2:p.Gly107AspfsTer?
NM_005514.8:c.319_320insAC MANE Select NP_005505.2:p.Gly107AspfsTer?