Canonical Allele Identifier: CA2534217765

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356826_31356827insA , CM000668.2:g.31356826_31356827insA	GRCh38
NC_000006.11:g.31324603_31324604insA , CM000668.1:g.31324603_31324604insA	GRCh37
NC_000006.10:g.31432582_31432583insA	NCBI36
NG_023187.1:g.5386_5387insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1677_1678insT
ENST00000481849.6:n.1677_1678insT
ENST00000497377.6:n.1677_1678insT
ENST00000640094.2:c.204_205insT	ENSP00000491275.2:p.Glu69Ter
ENST00000696558.1:c.204_205insT	ENSP00000512716.1:p.Glu69Ter
ENST00000696559.1:c.204_205insT	ENSP00000512717.1:p.Glu69Ter
ENST00000696560.1:c.204_205insT	ENSP00000512718.1:p.Glu69Ter
ENST00000696561.1:c.204_205insT	ENSP00000512719.1:p.Glu69Ter
ENST00000696562.1:c.204_205insT	ENSP00000512720.1:p.Glu69Ter
ENST00000412585.7:c.204_205insT MANE Select	ENSP00000399168.2:p.Glu69Ter
ENST00000412585.6:c.204_205insT	ENSP00000399168.2:p.Glu69Ter
ENST00000434333.1:c.237_238insT	ENSP00000405931.1:p.Glu80Ter
ENST00000474381.1:n.79_80insT
ENST00000498007.1:n.225_226insT
ENST00000603274.1:n.180_181insA
NM_005514.6:c.204_205insT	NP_005505.2:p.Glu69Ter
XM_011514556.1:c.237_238insT	XP_011512858.1:p.Glu80Ter
XM_011514557.1:c.204_205insT	XP_011512859.1:p.Glu69Ter
XR_926175.1:n.214_215insT
NM_005514.7:c.204_205insT	NP_005505.2:p.Glu69Ter
NM_005514.8:c.204_205insT MANE Select	NP_005505.2:p.Glu69Ter