Canonical Allele Identifier: CA645561005

Gene: HLA-B

Linked Data

• COSMIC: COSM1443260

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355187dup , CM000668.2:g.31355187dup	GRCh38
NC_000006.11:g.31322964dup , CM000668.1:g.31322964dup	GRCh37
NC_000006.10:g.31430943dup	NCBI36
NG_023187.1:g.7027dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2980dup
ENST00000481849.6:n.2499dup
ENST00000497377.6:n.2406dup
ENST00000640094.2:c.895+131dup	ENSP00000491275.2:n.895+131dup
ENST00000696558.1:c.1002dup	ENSP00000512716.1:n.1002dup
ENST00000696559.1:c.933dup	ENSP00000512717.1:p.Val312CysfsTer22
ENST00000696560.1:c.933dup	ENSP00000512718.1:p.Val312CysfsTer22
ENST00000696561.1:c.933dup	ENSP00000512719.1:p.Val312CysfsTer22
ENST00000696562.1:c.933dup	ENSP00000512720.1:p.Val312CysfsTer22
ENST00000412585.7:c.933dup MANE Select	ENSP00000399168.2:p.Val312CysfsTer22
ENST00000640094.1:c.88+131dup	ENSP00000491275.1:n.88+131dup
ENST00000412585.6:c.933dup	ENSP00000399168.2:p.Val312CysfsTer22
ENST00000463574.1:n.524dup
NM_005514.6:c.933dup	NP_005505.2:p.Val312CysfsTer22
XM_011514556.1:c.966dup	XP_011512858.1:p.Val323CysfsTer22
XM_011514557.1:c.895+131dup	XP_011512859.1:n.895+131dup
XR_926175.1:n.1372dup
NM_005514.7:c.933dup	NP_005505.2:p.Val312CysfsTer22
NM_005514.8:c.933dup MANE Select	NP_005505.2:p.Val312CysfsTer22