Canonical Allele Identifier: CA2677957689

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356753-G-GAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356753_31356754insAGA , CM000668.2:g.31356753_31356754insAGA	GRCh38
NC_000006.11:g.31324530_31324531insAGA , CM000668.1:g.31324530_31324531insAGA	GRCh37
NC_000006.10:g.31432509_31432510insAGA	NCBI36
NG_023187.1:g.5459_5460insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1750_1751insTCT
ENST00000481849.6:n.1750_1751insTCT
ENST00000497377.6:n.1750_1751insTCT
ENST00000640094.2:c.277_278insTCT	ENSP00000491275.2:p.Ala93delinsValSer
ENST00000696558.1:c.277_278insTCT	ENSP00000512716.1:p.Ala93delinsValSer
ENST00000696559.1:c.277_278insTCT	ENSP00000512717.1:p.Ala93delinsValSer
ENST00000696560.1:c.277_278insTCT	ENSP00000512718.1:p.Ala93delinsValSer
ENST00000696561.1:c.277_278insTCT	ENSP00000512719.1:p.Ala93delinsValSer
ENST00000696562.1:c.277_278insTCT	ENSP00000512720.1:p.Ala93delinsValSer
ENST00000412585.7:c.277_278insTCT MANE Select	ENSP00000399168.2:p.Ala93delinsValSer
ENST00000412585.6:c.277_278insTCT	ENSP00000399168.2:p.Ala93delinsValSer
ENST00000434333.1:c.310_311insTCT	ENSP00000405931.1:p.Ala104delinsValSer
ENST00000474381.1:n.152_153insTCT
ENST00000498007.1:n.298_299insTCT
ENST00000603274.1:n.107_108insAGA
NM_005514.6:c.277_278insTCT	NP_005505.2:p.Ala93delinsValSer
XM_011514556.1:c.310_311insTCT	XP_011512858.1:p.Ala104delinsValSer
XM_011514557.1:c.277_278insTCT	XP_011512859.1:p.Ala93delinsValSer
XR_926175.1:n.287_288insTCT
NM_005514.7:c.277_278insTCT	NP_005505.2:p.Ala93delinsValSer
NM_005514.8:c.277_278insTCT MANE Select	NP_005505.2:p.Ala93delinsValSer