Canonical Allele Identifier: CA2770503786

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356364del , CM000668.2:g.31356364del	GRCh38
NC_000006.11:g.31324141del , CM000668.1:g.31324141del	GRCh37
NC_000006.10:g.31432120del	NCBI36
NG_023187.1:g.5850del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1896del
ENST00000481849.6:n.1896del
ENST00000497377.6:n.1896del
ENST00000640094.2:c.423del	ENSP00000491275.2:p.Tyr142ThrfsTer9
ENST00000696558.1:c.423del	ENSP00000512716.1:p.Tyr142ThrfsTer9
ENST00000696559.1:c.423del	ENSP00000512717.1:p.Tyr142ThrfsTer9
ENST00000696560.1:c.423del	ENSP00000512718.1:p.Tyr142ThrfsTer9
ENST00000696561.1:c.423del	ENSP00000512719.1:p.Tyr142ThrfsTer9
ENST00000696562.1:c.423del	ENSP00000512720.1:p.Tyr142ThrfsTer9
ENST00000412585.7:c.423del MANE Select	ENSP00000399168.2:p.Tyr142ThrfsTer9
ENST00000412585.6:c.423del	ENSP00000399168.2:p.Tyr142ThrfsTer9
ENST00000434333.1:c.456del	ENSP00000405931.1:p.Tyr153ThrfsTer9
ENST00000474381.1:n.298del
ENST00000498007.1:n.689del
NM_005514.6:c.423del	NP_005505.2:p.Tyr142ThrfsTer9
XM_011514556.1:c.456del	XP_011512858.1:p.Tyr153ThrfsTer9
XM_011514557.1:c.423del	XP_011512859.1:p.Tyr142ThrfsTer9
XR_926175.1:n.433del
NM_005514.7:c.423del	NP_005505.2:p.Tyr142ThrfsTer9
NM_005514.8:c.423del MANE Select	NP_005505.2:p.Tyr142ThrfsTer9