Canonical Allele Identifier: CA1619118167

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355132_31355134delinsAGC , CM000668.2:g.31355132_31355134delinsAGC	GRCh38
NC_000006.11:g.31322909_31322911delinsAGC , CM000668.1:g.31322909_31322911delinsAGC	GRCh37
NC_000006.10:g.31430888_31430890delinsAGC	NCBI36
NG_023187.1:g.7079_7081delinsGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3032_3034delinsGCT
ENST00000481849.6:n.2551_2553delinsGCT
ENST00000497377.6:n.2458_2460delinsGCT
ENST00000640094.2:c.895+183_895+185delinsGCT	ENSP00000491275.2:n.895+183_895+185delins...
ENST00000696558.1:c.1054_1056delinsGCT	ENSP00000512716.1:n.1054_1056delinsGCT
ENST00000696559.1:c.985_987delinsGCT	ENSP00000512717.1:p.Ala329=
ENST00000696560.1:c.985_987delinsGCT	ENSP00000512718.1:p.Ala329=
ENST00000696561.1:c.985_987delinsGCT	ENSP00000512719.1:p.Ala329=
ENST00000696562.1:c.985_987delinsGCT	ENSP00000512720.1:p.Ala329=
ENST00000412585.7:c.985_987delinsGCT MANE Select	ENSP00000399168.2:p.Ala329=
ENST00000640094.1:c.88+183_88+185delinsGCT	ENSP00000491275.1:n.88+183_88+185delinsGC...
ENST00000412585.6:c.985_987delinsGCT	ENSP00000399168.2:p.Ala329=
ENST00000463574.1:n.576_578delinsGCT
NM_005514.6:c.985_987delinsGCT	NP_005505.2:p.Ala329=
XM_011514556.1:c.1018_1020delinsGCT	XP_011512858.1:p.Ala340=
XM_011514557.1:c.895+183_895+185delinsGCT	XP_011512859.1:n.895+183_895+185delinsGCT...
XR_926175.1:n.1424_1426delinsGCT
NM_005514.7:c.985_987delinsGCT	NP_005505.2:p.Ala329=
NM_005514.8:c.985_987delinsGCT MANE Select	NP_005505.2:p.Ala329=