Canonical Allele Identifier: CA2770503541

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354634del , CM000668.2:g.31354634del	GRCh38
NC_000006.11:g.31322411del , CM000668.1:g.31322411del	GRCh37
NC_000006.10:g.31430390del	NCBI36
NG_023187.1:g.7579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3091del
ENST00000481849.6:n.3051del
ENST00000497377.6:n.2958del
ENST00000640094.2:c.927del	ENSP00000491275.2:p.Cys310AlafsTer?
ENST00000696558.1:c.1113del	ENSP00000512716.1:n.1113del
ENST00000696559.1:c.1044del	ENSP00000512717.1:p.Cys349AlafsTer23
ENST00000696560.1:c.1044del	ENSP00000512718.1:p.Cys349AlafsTer23
ENST00000696561.1:c.1044del	ENSP00000512719.1:p.Cys349AlafsTer23
ENST00000696562.1:c.1044del	ENSP00000512720.1:p.Cys349AlafsTer23
ENST00000412585.7:c.1044del MANE Select	ENSP00000399168.2:p.Cys349AlafsTer23
ENST00000640094.1:c.120del	ENSP00000491275.1:p.Cys41AlafsTer?
ENST00000412585.6:c.1044del	ENSP00000399168.2:p.Cys349AlafsTer23
ENST00000481849.5:n.173del
ENST00000497377.5:n.443del
NM_005514.6:c.1044del	NP_005505.2:p.Cys349AlafsTer23
XM_011514556.1:c.1077del	XP_011512858.1:p.Cys360AlafsTer23
XM_011514557.1:c.927del	XP_011512859.1:p.Cys310AlafsTer23
XR_926175.1:n.1483del
NM_005514.7:c.1044del	NP_005505.2:p.Cys349AlafsTer23
NM_005514.8:c.1044del MANE Select	NP_005505.2:p.Cys349AlafsTer23