Canonical Allele Identifier: CA1619117991

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355029_31355030delinsAG , CM000668.2:g.31355029_31355030delinsAG	GRCh38
NC_000006.11:g.31322806_31322807delinsAG , CM000668.1:g.31322806_31322807delinsAG	GRCh37
NC_000006.10:g.31430785_31430786delinsAG	NCBI36
NG_023187.1:g.7183_7184delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+77_3059+78delinsCT
ENST00000481849.6:n.2655_2656delinsCT
ENST00000497377.6:n.2562_2563delinsCT
ENST00000640094.2:c.895+287_895+288delinsCT	ENSP00000491275.2:n.895+287_895+288delinsCT
ENST00000696558.1:c.1081+77_1081+78delinsCT	ENSP00000512716.1:n.1081+77_1081+78delinsCT
ENST00000696559.1:c.1012+77_1012+78delinsCT	ENSP00000512717.1:n.1012+77_1012+78delinsCT
ENST00000696560.1:c.1012+77_1012+78delinsCT	ENSP00000512718.1:n.1012+77_1012+78delinsCT
ENST00000696561.1:c.1012+77_1012+78delinsCT	ENSP00000512719.1:n.1012+77_1012+78delinsCT
ENST00000696562.1:c.1012+77_1012+78delinsCT	ENSP00000512720.1:n.1012+77_1012+78delinsCT
ENST00000412585.7:c.1012+77_1012+78delinsCT MANE Select	ENSP00000399168.2:n.1012+77_1012+78delinsCT
ENST00000640094.1:c.88+287_88+288delinsCT	ENSP00000491275.1:n.88+287_88+288delinsCT
ENST00000412585.6:c.1012+77_1012+78delinsCT	ENSP00000399168.2:n.1012+77_1012+78delinsCT
ENST00000497377.5:n.47_48delinsCT
NM_005514.6:c.1012+77_1012+78delinsCT	NP_005505.2:n.1012+77_1012+78delinsCT
XM_011514556.1:c.1045+77_1045+78delinsCT	XP_011512858.1:n.1045+77_1045+78delinsCT
XM_011514557.1:c.895+287_895+288delinsCT	XP_011512859.1:n.895+287_895+288delinsCT
XR_926175.1:n.1451+77_1451+78delinsCT
NM_005514.7:c.1012+77_1012+78delinsCT	NP_005505.2:n.1012+77_1012+78delinsCT
NM_005514.8:c.1012+77_1012+78delinsCT MANE Select	NP_005505.2:n.1012+77_1012+78delinsCT