Canonical Allele Identifier: CA2677954926

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355111-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355111_31355112insG , CM000668.2:g.31355111_31355112insG	GRCh38
NC_000006.11:g.31322888_31322889insG , CM000668.1:g.31322888_31322889insG	GRCh37
NC_000006.10:g.31430867_31430868insG	NCBI36
NG_023187.1:g.7101_7102insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3054_3055insC
ENST00000481849.6:n.2573_2574insC
ENST00000497377.6:n.2480_2481insC
ENST00000640094.2:c.895+205_895+206insC	ENSP00000491275.2:n.895+205_895+206insC
ENST00000696558.1:c.1076_1077insC	ENSP00000512716.1:n.1076_1077insC
ENST00000696559.1:c.1007_1008insC	ENSP00000512717.1:p.Ser337PhefsTer21
ENST00000696560.1:c.1007_1008insC	ENSP00000512718.1:p.Ser337PhefsTer21
ENST00000696561.1:c.1007_1008insC	ENSP00000512719.1:p.Ser337PhefsTer21
ENST00000696562.1:c.1007_1008insC	ENSP00000512720.1:p.Ser337PhefsTer21
ENST00000412585.7:c.1007_1008insC MANE Select	ENSP00000399168.2:p.Ser337PhefsTer21
ENST00000640094.1:c.88+205_88+206insC	ENSP00000491275.1:n.88+205_88+206insC
ENST00000412585.6:c.1007_1008insC	ENSP00000399168.2:p.Ser337PhefsTer21
NM_005514.6:c.1007_1008insC	NP_005505.2:p.Ser337PhefsTer21
XM_011514556.1:c.1040_1041insC	XP_011512858.1:p.Ser348PhefsTer21
XM_011514557.1:c.895+205_895+206insC	XP_011512859.1:n.895+205_895+206insC
XR_926175.1:n.1446_1447insC
NM_005514.7:c.1007_1008insC	NP_005505.2:p.Ser337PhefsTer21
NM_005514.8:c.1007_1008insC MANE Select	NP_005505.2:p.Ser337PhefsTer21