Canonical Allele Identifier: CA1087469618

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356765-T-TCG
• gnomAD v4: 6-31356765-T-TCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356765_31356766insCG , CM000668.2:g.31356765_31356766insCG	GRCh38
NC_000006.11:g.31324542_31324543insCG , CM000668.1:g.31324542_31324543insCG	GRCh37
NC_000006.10:g.31432521_31432522insCG	NCBI36
NG_023187.1:g.5447_5448insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1738_1739insCG
ENST00000481849.6:n.1738_1739insCG
ENST00000497377.6:n.1738_1739insCG
ENST00000640094.2:c.265_266insCG	ENSP00000491275.2:p.Gln89ProfsTer?
ENST00000696558.1:c.265_266insCG	ENSP00000512716.1:p.Gln89ProfsTer?
ENST00000696559.1:c.265_266insCG	ENSP00000512717.1:p.Gln89ProfsTer?
ENST00000696560.1:c.265_266insCG	ENSP00000512718.1:p.Gln89ProfsTer?
ENST00000696561.1:c.265_266insCG	ENSP00000512719.1:p.Gln89ProfsTer?
ENST00000696562.1:c.265_266insCG	ENSP00000512720.1:p.Gln89ProfsTer?
ENST00000412585.7:c.265_266insCG MANE Select	ENSP00000399168.2:p.Gln89ProfsTer?
ENST00000412585.6:c.265_266insCG	ENSP00000399168.2:p.Gln89ProfsTer?
ENST00000434333.1:c.298_299insCG	ENSP00000405931.1:p.Gln100ProfsTer?
ENST00000474381.1:n.140_141insCG
ENST00000498007.1:n.286_287insCG
ENST00000603274.1:n.119_120insCG
NM_005514.6:c.265_266insCG	NP_005505.2:p.Gln89ProfsTer?
XM_011514556.1:c.298_299insCG	XP_011512858.1:p.Gln100ProfsTer?
XM_011514557.1:c.265_266insCG	XP_011512859.1:p.Gln89ProfsTer?
XR_926175.1:n.275_276insCG
NM_005514.7:c.265_266insCG	NP_005505.2:p.Gln89ProfsTer?
NM_005514.8:c.265_266insCG MANE Select	NP_005505.2:p.Gln89ProfsTer?