Canonical Allele Identifier: CA1619118169

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355132_31355133delinsAG , CM000668.2:g.31355132_31355133delinsAG	GRCh38
NC_000006.11:g.31322909_31322910delinsAG , CM000668.1:g.31322909_31322910delinsAG	GRCh37
NC_000006.10:g.31430888_31430889delinsAG	NCBI36
NG_023187.1:g.7080_7081delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3033_3034delinsCT
ENST00000481849.6:n.2552_2553delinsCT
ENST00000497377.6:n.2459_2460delinsCT
ENST00000640094.2:c.895+184_895+185delinsCT	ENSP00000491275.2:n.895+184_895+185delinsCT
ENST00000696558.1:c.1055_1056delinsCT	ENSP00000512716.1:n.1055_1056delinsCT
ENST00000696559.1:c.986_987delinsCT	ENSP00000512717.1:p.Ala329=
ENST00000696560.1:c.986_987delinsCT	ENSP00000512718.1:p.Ala329=
ENST00000696561.1:c.986_987delinsCT	ENSP00000512719.1:p.Ala329=
ENST00000696562.1:c.986_987delinsCT	ENSP00000512720.1:p.Ala329=
ENST00000412585.7:c.986_987delinsCT MANE Select	ENSP00000399168.2:p.Ala329=
ENST00000640094.1:c.88+184_88+185delinsCT	ENSP00000491275.1:n.88+184_88+185delinsCT
ENST00000412585.6:c.986_987delinsCT	ENSP00000399168.2:p.Ala329=
ENST00000463574.1:n.577_578delinsCT
NM_005514.6:c.986_987delinsCT	NP_005505.2:p.Ala329=
XM_011514556.1:c.1019_1020delinsCT	XP_011512858.1:p.Ala340=
XM_011514557.1:c.895+184_895+185delinsCT	XP_011512859.1:n.895+184_895+185delinsCT
XR_926175.1:n.1425_1426delinsCT
NM_005514.7:c.986_987delinsCT	NP_005505.2:p.Ala329=
NM_005514.8:c.986_987delinsCT MANE Select	NP_005505.2:p.Ala329=