Canonical Allele Identifier: CA645561006

Gene: HLA-B

Linked Data

• COSMIC: COSM3722057

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355193_31355194del , CM000668.2:g.31355193_31355194del	GRCh38
NC_000006.11:g.31322970_31322971del , CM000668.1:g.31322970_31322971del	GRCh37
NC_000006.10:g.31430949_31430950del	NCBI36
NG_023187.1:g.7020_7021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2973_2974del
ENST00000481849.6:n.2492_2493del
ENST00000497377.6:n.2399_2400del
ENST00000640094.2:c.895+124_895+125del	ENSP00000491275.2:n.895+124_895+125del
ENST00000696558.1:c.995_996del	ENSP00000512716.1:n.995_996del
ENST00000696559.1:c.926_927del	ENSP00000512717.1:p.Val309GlyfsTer24
ENST00000696560.1:c.926_927del	ENSP00000512718.1:p.Val309GlyfsTer24
ENST00000696561.1:c.926_927del	ENSP00000512719.1:p.Val309GlyfsTer24
ENST00000696562.1:c.926_927del	ENSP00000512720.1:p.Val309GlyfsTer24
ENST00000412585.7:c.926_927del MANE Select	ENSP00000399168.2:p.Val309GlyfsTer24
ENST00000640094.1:c.88+124_88+125del	ENSP00000491275.1:n.88+124_88+125del
ENST00000412585.6:c.926_927del	ENSP00000399168.2:p.Val309GlyfsTer24
ENST00000463574.1:n.517_518del
NM_005514.6:c.926_927del	NP_005505.2:p.Val309GlyfsTer24
XM_011514556.1:c.959_960del	XP_011512858.1:p.Val320GlyfsTer24
XM_011514557.1:c.895+124_895+125del	XP_011512859.1:n.895+124_895+125del
XR_926175.1:n.1365_1366del
NM_005514.7:c.926_927del	NP_005505.2:p.Val309GlyfsTer24
NM_005514.8:c.926_927del MANE Select	NP_005505.2:p.Val309GlyfsTer24