Canonical Allele Identifier: CA1619117537

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354649_31354653delinsGCTCC , CM000668.2:g.31354649_31354653delinsGCTCC	GRCh38
NC_000006.11:g.31322426_31322430delinsGCTCC , CM000668.1:g.31322426_31322430delinsGCTCC	GRCh37
NC_000006.10:g.31430405_31430409delinsGCTCC	NCBI36
NG_023187.1:g.7560_7564delinsGGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3072_3076delinsGGAGC
ENST00000481849.6:n.3032_3036delinsGGAGC
ENST00000497377.6:n.2939_2943delinsGGAGC
ENST00000640094.2:c.908_912delinsGGAGC	ENSP00000491275.2:p.Gly303=
ENST00000696558.1:c.1094_1098delinsGGAGC	ENSP00000512716.1:n.1094_1098delinsGGAGC
ENST00000696559.1:c.1025_1029delinsGGAGC	ENSP00000512717.1:p.Gly342=
ENST00000696560.1:c.1025_1029delinsGGAGC	ENSP00000512718.1:p.Gly342=
ENST00000696561.1:c.1025_1029delinsGGAGC	ENSP00000512719.1:p.Gly342=
ENST00000696562.1:c.1025_1029delinsGGAGC	ENSP00000512720.1:p.Gly342=
ENST00000412585.7:c.1025_1029delinsGGAGC MANE Select	ENSP00000399168.2:p.Gly342=
ENST00000640094.1:c.101_105delinsGGAGC	ENSP00000491275.1:p.Gly34=
ENST00000412585.6:c.1025_1029delinsGGAGC	ENSP00000399168.2:p.Gly342=
ENST00000481849.5:n.154_158delinsGGAGC
ENST00000497377.5:n.424_428delinsGGAGC
NM_005514.6:c.1025_1029delinsGGAGC	NP_005505.2:p.Gly342=
XM_011514556.1:c.1058_1062delinsGGAGC	XP_011512858.1:p.Gly353=
XM_011514557.1:c.908_912delinsGGAGC	XP_011512859.1:p.Gly303=
XR_926175.1:n.1464_1468delinsGGAGC
NM_005514.7:c.1025_1029delinsGGAGC	NP_005505.2:p.Gly342=
NM_005514.8:c.1025_1029delinsGGAGC MANE Select	NP_005505.2:p.Gly342=