Canonical Allele Identifier: CA2677954969

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355131-C-CAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133_31355134insTAG , CM000668.2:g.31355133_31355134insTAG	GRCh38
NC_000006.11:g.31322910_31322911insTAG , CM000668.1:g.31322910_31322911insTAG	GRCh37
NC_000006.10:g.31430889_31430890insTAG	NCBI36
NG_023187.1:g.7081_7082insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3034_3035insACT
ENST00000481849.6:n.2553_2554insACT
ENST00000497377.6:n.2460_2461insACT
ENST00000640094.2:c.895+185_895+186insACT	ENSP00000491275.2:n.895+185_895+186insACT
ENST00000696558.1:c.1056_1057insACT	ENSP00000512716.1:n.1056_1057insACT
ENST00000696559.1:c.987_988insACT	ENSP00000512717.1:p.Ala329_Val330insThr
ENST00000696560.1:c.987_988insACT	ENSP00000512718.1:p.Ala329_Val330insThr
ENST00000696561.1:c.987_988insACT	ENSP00000512719.1:p.Ala329_Val330insThr
ENST00000696562.1:c.987_988insACT	ENSP00000512720.1:p.Ala329_Val330insThr
ENST00000412585.7:c.987_988insACT MANE Select	ENSP00000399168.2:p.Ala329_Val330insThr
ENST00000640094.1:c.88+185_88+186insACT	ENSP00000491275.1:n.88+185_88+186insACT
ENST00000412585.6:c.987_988insACT	ENSP00000399168.2:p.Ala329_Val330insThr
ENST00000463574.1:n.578_579insACT
NM_005514.6:c.987_988insACT	NP_005505.2:p.Ala329_Val330insThr
XM_011514556.1:c.1020_1021insACT	XP_011512858.1:p.Ala340_Val341insThr
XM_011514557.1:c.895+185_895+186insACT	XP_011512859.1:n.895+185_895+186insACT
XR_926175.1:n.1426_1427insACT
NM_005514.7:c.987_988insACT	NP_005505.2:p.Ala329_Val330insThr
NM_005514.8:c.987_988insACT MANE Select	NP_005505.2:p.Ala329_Val330insThr