Canonical Allele Identifier: CA1087464736

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355184-A-AGGACAGCTGGG
• gnomAD v4: 6-31355184-A-AGGACAGCTGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355184_31355185insGGACAGCTGGG , CM000668.2:g.31355184_31355185insGGACAGCTGGG	GRCh38
NC_000006.11:g.31322961_31322962insGGACAGCTGGG , CM000668.1:g.31322961_31322962insGGACAGCTGGG	GRCh37
NC_000006.10:g.31430940_31430941insGGACAGCTGGG	NCBI36
NG_023187.1:g.7028_7029insCCCAGCTGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2981_2982insCCCAGCTGTCC
ENST00000481849.6:n.2500_2501insCCCAGCTGTCC
ENST00000497377.6:n.2407_2408insCCCAGCTGTCC
ENST00000640094.2:c.895+132_895+133insCCCAGCTGTCC	ENSP00000491275.2:n.895+132_895+133insCCCAGCTGTCC
ENST00000696558.1:c.1003_1004insCCCAGCTGTCC	ENSP00000512716.1:n.1003_1004insCCCAGCTGTCC
ENST00000696559.1:c.934_935insCCCAGCTGTCC	ENSP00000512717.1:p.Val312AlafsTer11
ENST00000696560.1:c.934_935insCCCAGCTGTCC	ENSP00000512718.1:p.Val312AlafsTer11
ENST00000696561.1:c.934_935insCCCAGCTGTCC	ENSP00000512719.1:p.Val312AlafsTer11
ENST00000696562.1:c.934_935insCCCAGCTGTCC	ENSP00000512720.1:p.Val312AlafsTer11
ENST00000412585.7:c.934_935insCCCAGCTGTCC MANE Select	ENSP00000399168.2:p.Val312AlafsTer11
ENST00000640094.1:c.88+132_88+133insCCCAGCTGTCC	ENSP00000491275.1:n.88+132_88+133insCCCAGCTGTCC
ENST00000412585.6:c.934_935insCCCAGCTGTCC	ENSP00000399168.2:p.Val312AlafsTer11
ENST00000463574.1:n.525_526insCCCAGCTGTCC
NM_005514.6:c.934_935insCCCAGCTGTCC	NP_005505.2:p.Val312AlafsTer11
XM_011514556.1:c.967_968insCCCAGCTGTCC	XP_011512858.1:p.Val323AlafsTer11
XM_011514557.1:c.895+132_895+133insCCCAGCTGTCC	XP_011512859.1:n.895+132_895+133insCCCAGCTGTCC
XR_926175.1:n.1373_1374insCCCAGCTGTCC
NM_005514.7:c.934_935insCCCAGCTGTCC	NP_005505.2:p.Val312AlafsTer11
NM_005514.8:c.934_935insCCCAGCTGTCC MANE Select	NP_005505.2:p.Val312AlafsTer11