Canonical Allele Identifier: CA645561015

Gene: HLA-B

Linked Data

• COSMIC: COSM5367700

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355585dup , CM000668.2:g.31355585dup	GRCh38
NC_000006.11:g.31323362dup , CM000668.1:g.31323362dup	GRCh37
NC_000006.10:g.31431341dup	NCBI36
NG_023187.1:g.6630dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2676dup
ENST00000481849.6:n.2102dup
ENST00000497377.6:n.2102dup
ENST00000640094.2:c.629dup	ENSP00000491275.2:p.Thr211AspfsTer10
ENST00000696558.1:c.698dup	ENSP00000512716.1:n.698dup
ENST00000696559.1:c.629dup	ENSP00000512717.1:p.Thr211AspfsTer10
ENST00000696560.1:c.629dup	ENSP00000512718.1:p.Thr211AspfsTer10
ENST00000696561.1:c.629dup	ENSP00000512719.1:p.Thr211AspfsTer10
ENST00000696562.1:c.629dup	ENSP00000512720.1:p.Thr211AspfsTer10
ENST00000412585.7:c.629dup MANE Select	ENSP00000399168.2:p.Thr211AspfsTer10
ENST00000412585.6:c.629dup	ENSP00000399168.2:p.Thr211AspfsTer10
ENST00000434333.1:c.662dup	ENSP00000405931.1:p.Thr222AspfsTer10
ENST00000463574.1:n.220dup
ENST00000474381.1:n.1078dup
ENST00000498007.1:n.895dup
NM_005514.6:c.629dup	NP_005505.2:p.Thr211AspfsTer10
XM_011514556.1:c.662dup	XP_011512858.1:p.Thr222AspfsTer10
XM_011514557.1:c.629dup	XP_011512859.1:p.Thr211AspfsTer10
XR_926175.1:n.1068dup
NM_005514.7:c.629dup	NP_005505.2:p.Thr211AspfsTer10
NM_005514.8:c.629dup MANE Select	NP_005505.2:p.Thr211AspfsTer10