Canonical Allele Identifier: CA2677954921

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355109-G-GAGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355110_31355111insGCAA , CM000668.2:g.31355110_31355111insGCAA	GRCh38
NC_000006.11:g.31322887_31322888insGCAA , CM000668.1:g.31322887_31322888insGCAA	GRCh37
NC_000006.10:g.31430866_31430867insGCAA	NCBI36
NG_023187.1:g.7103_7104insTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3056_3057insTGCT
ENST00000481849.6:n.2575_2576insTGCT
ENST00000497377.6:n.2482_2483insTGCT
ENST00000640094.2:c.895+207_895+208insTGCT	ENSP00000491275.2:n.895+207_895+208insTGCT
ENST00000696558.1:c.1078_1079insTGCT	ENSP00000512716.1:n.1078_1079insTGCT
ENST00000696559.1:c.1009_1010insTGCT	ENSP00000512717.1:p.Ser337LeufsTer22
ENST00000696560.1:c.1009_1010insTGCT	ENSP00000512718.1:p.Ser337LeufsTer22
ENST00000696561.1:c.1009_1010insTGCT	ENSP00000512719.1:p.Ser337LeufsTer22
ENST00000696562.1:c.1009_1010insTGCT	ENSP00000512720.1:p.Ser337LeufsTer22
ENST00000412585.7:c.1009_1010insTGCT MANE Select	ENSP00000399168.2:p.Ser337LeufsTer22
ENST00000640094.1:c.88+207_88+208insTGCT	ENSP00000491275.1:n.88+207_88+208insTGCT
ENST00000412585.6:c.1009_1010insTGCT	ENSP00000399168.2:p.Ser337LeufsTer22
NM_005514.6:c.1009_1010insTGCT	NP_005505.2:p.Ser337LeufsTer22
XM_011514556.1:c.1042_1043insTGCT	XP_011512858.1:p.Ser348LeufsTer22
XM_011514557.1:c.895+207_895+208insTGCT	XP_011512859.1:n.895+207_895+208insTGCT
XR_926175.1:n.1448_1449insTGCT
NM_005514.7:c.1009_1010insTGCT	NP_005505.2:p.Ser337LeufsTer22
NM_005514.8:c.1009_1010insTGCT MANE Select	NP_005505.2:p.Ser337LeufsTer22