Canonical Allele Identifier: CA2677954689

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355002-G-GTGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355004_31355005insGATG , CM000668.2:g.31355004_31355005insGATG	GRCh38
NC_000006.11:g.31322781_31322782insGATG , CM000668.1:g.31322781_31322782insGATG	GRCh37
NC_000006.10:g.31430760_31430761insGATG	NCBI36
NG_023187.1:g.7210_7211insTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+104_3059+105insTCCA
ENST00000481849.6:n.2682_2683insTCCA
ENST00000497377.6:n.2589_2590insTCCA
ENST00000640094.2:c.895+314_895+315insTCCA	ENSP00000491275.2:n.895+314_895+315insTCCA
ENST00000696558.1:c.1081+104_1081+105insTCCA	ENSP00000512716.1:n.1081+104_1081+105insTCCA
ENST00000696559.1:c.1012+104_1012+105insTCCA	ENSP00000512717.1:n.1012+104_1012+105insTCCA
ENST00000696560.1:c.1012+104_1012+105insTCCA	ENSP00000512718.1:n.1012+104_1012+105insTCCA
ENST00000696561.1:c.1012+104_1012+105insTCCA	ENSP00000512719.1:n.1012+104_1012+105insTCCA
ENST00000696562.1:c.1012+104_1012+105insTCCA	ENSP00000512720.1:n.1012+104_1012+105insTCCA
ENST00000412585.7:c.1012+104_1012+105insTCCA MANE Select	ENSP00000399168.2:n.1012+104_1012+105insTCCA
ENST00000640094.1:c.88+314_88+315insTCCA	ENSP00000491275.1:n.88+314_88+315insTCCA
ENST00000412585.6:c.1012+104_1012+105insTCCA	ENSP00000399168.2:n.1012+104_1012+105insTCCA
ENST00000497377.5:n.74_75insTCCA
NM_005514.6:c.1012+104_1012+105insTCCA	NP_005505.2:n.1012+104_1012+105insTCCA
XM_011514556.1:c.1045+104_1045+105insTCCA	XP_011512858.1:n.1045+104_1045+105insTCCA
XM_011514557.1:c.895+314_895+315insTCCA	XP_011512859.1:n.895+314_895+315insTCCA
XR_926175.1:n.1451+104_1451+105insTCCA
NM_005514.7:c.1012+104_1012+105insTCCA	NP_005505.2:n.1012+104_1012+105insTCCA
NM_005514.8:c.1012+104_1012+105insTCCA MANE Select	NP_005505.2:n.1012+104_1012+105insTCCA