Canonical Allele Identifier: CA1619112859

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356717_31356720delinsAGGT , CM000668.2:g.31356717_31356720delinsAGGT	GRCh38
NC_000006.11:g.31324494_31324497delinsAGGT , CM000668.1:g.31324494_31324497delinsAGGT	GRCh37
NC_000006.10:g.31432473_31432476delinsAGGT	NCBI36
NG_023187.1:g.5493_5496delinsACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1784_1787delinsACCT
ENST00000481849.6:n.1784_1787delinsACCT
ENST00000497377.6:n.1784_1787delinsACCT
ENST00000640094.2:c.311_314delinsACCT	ENSP00000491275.2:p.Asn104=
ENST00000696558.1:c.311_314delinsACCT	ENSP00000512716.1:p.Asn104=
ENST00000696559.1:c.311_314delinsACCT	ENSP00000512717.1:p.Asn104=
ENST00000696560.1:c.311_314delinsACCT	ENSP00000512718.1:p.Asn104=
ENST00000696561.1:c.311_314delinsACCT	ENSP00000512719.1:p.Asn104=
ENST00000696562.1:c.311_314delinsACCT	ENSP00000512720.1:p.Asn104=
ENST00000412585.7:c.311_314delinsACCT MANE Select	ENSP00000399168.2:p.Asn104=
ENST00000412585.6:c.311_314delinsACCT	ENSP00000399168.2:p.Asn104=
ENST00000434333.1:c.344_347delinsACCT	ENSP00000405931.1:p.Asn115=
ENST00000474381.1:n.186_189delinsACCT
ENST00000498007.1:n.332_335delinsACCT
ENST00000603274.1:n.71_74delinsAGGT
NM_005514.6:c.311_314delinsACCT	NP_005505.2:p.Asn104=
XM_011514556.1:c.344_347delinsACCT	XP_011512858.1:p.Asn115=
XM_011514557.1:c.311_314delinsACCT	XP_011512859.1:p.Asn104=
XR_926175.1:n.321_324delinsACCT
NM_005514.7:c.311_314delinsACCT	NP_005505.2:p.Asn104=
NM_005514.8:c.311_314delinsACCT MANE Select	NP_005505.2:p.Asn104=