Canonical Allele Identifier: CA2677954978

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355133-G-GTAGCGACCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133_31355134insTAGCGACCA , CM000668.2:g.31355133_31355134insTAGCGACCA	GRCh38
NC_000006.11:g.31322910_31322911insTAGCGACCA , CM000668.1:g.31322910_31322911insTAGCGACCA	GRCh37
NC_000006.10:g.31430889_31430890insTAGCGACCA	NCBI36
NG_023187.1:g.7079_7080insTGGTCGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3032_3033insTGGTCGCTA
ENST00000481849.6:n.2551_2552insTGGTCGCTA
ENST00000497377.6:n.2458_2459insTGGTCGCTA
ENST00000640094.2:c.895+183_895+184insTGGTCGCTA	ENSP00000491275.2:n.895+183_895+184insTGGTCGCTA
ENST00000696558.1:c.1054_1055insTGGTCGCTA	ENSP00000512716.1:n.1054_1055insTGGTCGCTA
ENST00000696559.1:c.985_986insTGGTCGCTA	ENSP00000512717.1:p.Ala329delinsValValAlaThr
ENST00000696560.1:c.985_986insTGGTCGCTA	ENSP00000512718.1:p.Ala329delinsValValAlaThr
ENST00000696561.1:c.985_986insTGGTCGCTA	ENSP00000512719.1:p.Ala329delinsValValAlaThr
ENST00000696562.1:c.985_986insTGGTCGCTA	ENSP00000512720.1:p.Ala329delinsValValAlaThr
ENST00000412585.7:c.985_986insTGGTCGCTA MANE Select	ENSP00000399168.2:p.Ala329delinsValValAlaThr
ENST00000640094.1:c.88+183_88+184insTGGTCGCTA	ENSP00000491275.1:n.88+183_88+184insTGGTCGCTA
ENST00000412585.6:c.985_986insTGGTCGCTA	ENSP00000399168.2:p.Ala329delinsValValAlaThr
ENST00000463574.1:n.576_577insTGGTCGCTA
NM_005514.6:c.985_986insTGGTCGCTA	NP_005505.2:p.Ala329delinsValValAlaThr
XM_011514556.1:c.1018_1019insTGGTCGCTA	XP_011512858.1:p.Ala340delinsValValAlaThr
XM_011514557.1:c.895+183_895+184insTGGTCGCTA	XP_011512859.1:n.895+183_895+184insTGGTCGCTA
XR_926175.1:n.1424_1425insTGGTCGCTA
NM_005514.7:c.985_986insTGGTCGCTA	NP_005505.2:p.Ala329delinsValValAlaThr
NM_005514.8:c.985_986insTGGTCGCTA MANE Select	NP_005505.2:p.Ala329delinsValValAlaThr