Canonical Allele Identifier: CA1087469536
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356756_31356757insCC , CM000668.2:g.31356756_31356757insCC GRCh38
NC_000006.11:g.31324533_31324534insCC , CM000668.1:g.31324533_31324534insCC GRCh37
NC_000006.10:g.31432512_31432513insCC NCBI36
NG_023187.1:g.5456_5457insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1747_1748insGG
ENST00000481849.6:n.1747_1748insGG
ENST00000497377.6:n.1747_1748insGG
ENST00000640094.2:c.274_275insGG ENSP00000491275.2:p.Lys92ArgfsTer?
ENST00000696558.1:c.274_275insGG ENSP00000512716.1:p.Lys92ArgfsTer?
ENST00000696559.1:c.274_275insGG ENSP00000512717.1:p.Lys92ArgfsTer?
ENST00000696560.1:c.274_275insGG ENSP00000512718.1:p.Lys92ArgfsTer?
ENST00000696561.1:c.274_275insGG ENSP00000512719.1:p.Lys92ArgfsTer?
ENST00000696562.1:c.274_275insGG ENSP00000512720.1:p.Lys92ArgfsTer?
ENST00000412585.7:c.274_275insGG MANE Select ENSP00000399168.2:p.Lys92ArgfsTer?
ENST00000412585.6:c.274_275insGG ENSP00000399168.2:p.Lys92ArgfsTer?
ENST00000434333.1:c.307_308insGG ENSP00000405931.1:p.Lys103ArgfsTer?
ENST00000474381.1:n.149_150insGG
ENST00000498007.1:n.295_296insGG
ENST00000603274.1:n.110_111insCC
NM_005514.6:c.274_275insGG NP_005505.2:p.Lys92ArgfsTer?
XM_011514556.1:c.307_308insGG XP_011512858.1:p.Lys103ArgfsTer?
XM_011514557.1:c.274_275insGG XP_011512859.1:p.Lys92ArgfsTer?
XR_926175.1:n.284_285insGG
NM_005514.7:c.274_275insGG NP_005505.2:p.Lys92ArgfsTer?
NM_005514.8:c.274_275insGG MANE Select NP_005505.2:p.Lys92ArgfsTer?