Canonical Allele Identifier: CA1619116764

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354425_31354428delinsCCCA , CM000668.2:g.31354425_31354428delinsCCCA	GRCh38
NC_000006.11:g.31322202_31322205delinsCCCA , CM000668.1:g.31322202_31322205delinsCCCA	GRCh37
NC_000006.10:g.31430181_31430184delinsCCCA	NCBI36
NG_023187.1:g.7785_7788delinsTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+51_3140+54delinsTGGG
ENST00000481849.6:n.3100+51_3100+54delinsTGGG
ENST00000497377.6:n.3007+51_3007+54delinsTGGG
ENST00000696558.1:c.1162+51_1162+54delinsTGGG	ENSP00000512716.1:n.1162+51_1162+54delinsTGGG
ENST00000696559.1:c.*4+51_*4+54delinsTGGG	ENSP00000512717.1:n.*4+51_*4+54delinsTGGG
ENST00000696560.1:c.*4+51_*4+54delinsTGGG	ENSP00000512718.1:n.*4+51_*4+54delinsTGGG
ENST00000696561.1:c.*4+51_*4+54delinsTGGG	ENSP00000512719.1:n.*4+51_*4+54delinsTGGG
ENST00000696562.1:c.*4+51_*4+54delinsTGGG	ENSP00000512720.1:n.*4+51_*4+54delinsTGGG
ENST00000412585.7:c.*4+51_*4+54delinsTGGG MANE Select	ENSP00000399168.2:n.*4+51_*4+54delinsTGGG
ENST00000412585.6:c.*4+51_*4+54delinsTGGG	ENSP00000399168.2:n.*4+51_*4+54delinsTGGG
ENST00000481849.5:n.328+51_328+54delinsTGGG
ENST00000497377.5:n.492+51_492+54delinsTGGG
NM_005514.6:c.*4+51_*4+54delinsTGGG	NP_005505.2:n.*4+51_*4+54delinsTGGG
XM_011514556.1:c.*4+51_*4+54delinsTGGG	XP_011512858.1:n.*4+51_*4+54delinsTGGG
XM_011514557.1:c.*4+51_*4+54delinsTGGG	XP_011512859.1:n.*4+51_*4+54delinsTGGG
XR_926175.1:n.1532+51_1532+54delinsTGGG
NM_005514.7:c.*4+51_*4+54delinsTGGG	NP_005505.2:n.*4+51_*4+54delinsTGGG
NM_005514.8:c.*4+51_*4+54delinsTGGG MANE Select	NP_005505.2:n.*4+51_*4+54delinsTGGG