Canonical Allele Identifier: CA2770503705

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356218_31356221del , CM000668.2:g.31356218_31356221del	GRCh38
NC_000006.11:g.31323995_31323998del , CM000668.1:g.31323995_31323998del	GRCh37
NC_000006.10:g.31431974_31431977del	NCBI36
NG_023187.1:g.5992_5995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2038_2041del
ENST00000481849.6:n.2038_2041del
ENST00000497377.6:n.2038_2041del
ENST00000640094.2:c.565_568del	ENSP00000491275.2:p.Val189SerfsTer24
ENST00000696558.1:c.565_568del	ENSP00000512716.1:p.Val189SerfsTer?
ENST00000696559.1:c.565_568del	ENSP00000512717.1:p.Val189SerfsTer24
ENST00000696560.1:c.565_568del	ENSP00000512718.1:p.Val189SerfsTer24
ENST00000696561.1:c.565_568del	ENSP00000512719.1:p.Val189SerfsTer24
ENST00000696562.1:c.565_568del	ENSP00000512720.1:p.Val189SerfsTer24
ENST00000412585.7:c.565_568del MANE Select	ENSP00000399168.2:p.Val189SerfsTer24
ENST00000412585.6:c.565_568del	ENSP00000399168.2:p.Val189SerfsTer24
ENST00000434333.1:c.598_601del	ENSP00000405931.1:p.Val200SerfsTer24
ENST00000474381.1:n.440_443del
ENST00000498007.1:n.831_834del
NM_005514.6:c.565_568del	NP_005505.2:p.Val189SerfsTer24
XM_011514556.1:c.598_601del	XP_011512858.1:p.Val200SerfsTer24
XM_011514557.1:c.565_568del	XP_011512859.1:p.Val189SerfsTer24
XR_926175.1:n.575_578del
NM_005514.7:c.565_568del	NP_005505.2:p.Val189SerfsTer24
NM_005514.8:c.565_568del MANE Select	NP_005505.2:p.Val189SerfsTer24