Canonical Allele Identifier: CA2677957600

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356699-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356699_31356700insC , CM000668.2:g.31356699_31356700insC	GRCh38
NC_000006.11:g.31324476_31324477insC , CM000668.1:g.31324476_31324477insC	GRCh37
NC_000006.10:g.31432455_31432456insC	NCBI36
NG_023187.1:g.5513_5514insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1804_1805insG
ENST00000481849.6:n.1804_1805insG
ENST00000497377.6:n.1804_1805insG
ENST00000640094.2:c.331_332insG	ENSP00000491275.2:p.Gln111ArgfsTer28
ENST00000696558.1:c.331_332insG	ENSP00000512716.1:p.Gln111ArgfsTer28
ENST00000696559.1:c.331_332insG	ENSP00000512717.1:p.Gln111ArgfsTer28
ENST00000696560.1:c.331_332insG	ENSP00000512718.1:p.Gln111ArgfsTer28
ENST00000696561.1:c.331_332insG	ENSP00000512719.1:p.Gln111ArgfsTer28
ENST00000696562.1:c.331_332insG	ENSP00000512720.1:p.Gln111ArgfsTer28
ENST00000412585.7:c.331_332insG MANE Select	ENSP00000399168.2:p.Gln111ArgfsTer28
ENST00000412585.6:c.331_332insG	ENSP00000399168.2:p.Gln111ArgfsTer28
ENST00000434333.1:c.364_365insG	ENSP00000405931.1:p.Gln122ArgfsTer28
ENST00000474381.1:n.206_207insG
ENST00000498007.1:n.352_353insG
ENST00000603274.1:n.53_54insC
NM_005514.6:c.331_332insG	NP_005505.2:p.Gln111ArgfsTer28
XM_011514556.1:c.364_365insG	XP_011512858.1:p.Gln122ArgfsTer28
XM_011514557.1:c.331_332insG	XP_011512859.1:p.Gln111ArgfsTer28
XR_926175.1:n.341_342insG
NM_005514.7:c.331_332insG	NP_005505.2:p.Gln111ArgfsTer28
NM_005514.8:c.331_332insG MANE Select	NP_005505.2:p.Gln111ArgfsTer28