Canonical Allele Identifier: CA2677957897

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357112-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357112_31357113insAT , CM000668.2:g.31357112_31357113insAT	GRCh38
NC_000006.11:g.31324889_31324890insAT , CM000668.1:g.31324889_31324890insAT	GRCh37
NC_000006.10:g.31432868_31432869insAT	NCBI36
NG_023187.1:g.5100_5101insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1519_1520insAT
ENST00000481849.6:n.1519_1520insAT
ENST00000497377.6:n.1519_1520insAT
ENST00000640094.2:c.46_47insAT	ENSP00000491275.2:p.Ala16AspfsTer5
ENST00000696558.1:c.46_47insAT	ENSP00000512716.1:p.Ala16AspfsTer5
ENST00000696559.1:c.46_47insAT	ENSP00000512717.1:p.Ala16AspfsTer5
ENST00000696560.1:c.46_47insAT	ENSP00000512718.1:p.Ala16AspfsTer5
ENST00000696561.1:c.46_47insAT	ENSP00000512719.1:p.Ala16AspfsTer5
ENST00000696562.1:c.46_47insAT	ENSP00000512720.1:p.Ala16AspfsTer5
ENST00000412585.7:c.46_47insAT MANE Select	ENSP00000399168.2:p.Ala16AspfsTer5
ENST00000412585.6:c.46_47insAT	ENSP00000399168.2:p.Ala16AspfsTer5
ENST00000434333.1:c.-50_-49insAT	ENSP00000405931.1:n.-50_-49insAT
ENST00000498007.1:n.67_68insAT
ENST00000603274.1:n.466_467insAT
NM_005514.6:c.46_47insAT	NP_005505.2:p.Ala16AspfsTer5
XM_011514557.1:c.46_47insAT	XP_011512859.1:p.Ala16AspfsTer5
XR_926175.1:n.56_57insAT
NM_005514.7:c.46_47insAT	NP_005505.2:p.Ala16AspfsTer5
NM_005514.8:c.46_47insAT MANE Select	NP_005505.2:p.Ala16AspfsTer5