Canonical Allele Identifier: CA2770503829

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356707_31356713del , CM000668.2:g.31356707_31356713del	GRCh38
NC_000006.11:g.31324484_31324490del , CM000668.1:g.31324484_31324490del	GRCh37
NC_000006.10:g.31432463_31432469del	NCBI36
NG_023187.1:g.5500_5506del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1791_1797del
ENST00000481849.6:n.1791_1797del
ENST00000497377.6:n.1791_1797del
ENST00000640094.2:c.318_324del	ENSP00000491275.2:p.Gly107ThrfsTer?
ENST00000696558.1:c.318_324del	ENSP00000512716.1:p.Gly107ThrfsTer?
ENST00000696559.1:c.318_324del	ENSP00000512717.1:p.Gly107ThrfsTer?
ENST00000696560.1:c.318_324del	ENSP00000512718.1:p.Gly107ThrfsTer?
ENST00000696561.1:c.318_324del	ENSP00000512719.1:p.Gly107ThrfsTer?
ENST00000696562.1:c.318_324del	ENSP00000512720.1:p.Gly107ThrfsTer?
ENST00000412585.7:c.318_324del MANE Select	ENSP00000399168.2:p.Gly107ThrfsTer?
ENST00000412585.6:c.318_324del	ENSP00000399168.2:p.Gly107ThrfsTer?
ENST00000434333.1:c.351_357del	ENSP00000405931.1:p.Gly118ThrfsTer?
ENST00000474381.1:n.193_199del
ENST00000498007.1:n.339_345del
ENST00000603274.1:n.61_67del
NM_005514.6:c.318_324del	NP_005505.2:p.Gly107ThrfsTer?
XM_011514556.1:c.351_357del	XP_011512858.1:p.Gly118ThrfsTer?
XM_011514557.1:c.318_324del	XP_011512859.1:p.Gly107ThrfsTer?
XR_926175.1:n.328_334del
NM_005514.7:c.318_324del	NP_005505.2:p.Gly107ThrfsTer?
NM_005514.8:c.318_324del MANE Select	NP_005505.2:p.Gly107ThrfsTer?