Canonical Allele Identifier: CA2677957925

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357152-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357152_31357153insA , CM000668.2:g.31357152_31357153insA	GRCh38
NC_000006.11:g.31324929_31324930insA , CM000668.1:g.31324929_31324930insA	GRCh37
NC_000006.10:g.31432908_31432909insA	NCBI36
NG_023187.1:g.5060_5061insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1479_1480insT
ENST00000481849.6:n.1479_1480insT
ENST00000497377.6:n.1479_1480insT
ENST00000640094.2:c.6_7insT	ENSP00000491275.2:p.Val3CysfsTer?
ENST00000696558.1:c.6_7insT	ENSP00000512716.1:p.Val3CysfsTer?
ENST00000696559.1:c.6_7insT	ENSP00000512717.1:p.Val3CysfsTer?
ENST00000696560.1:c.6_7insT	ENSP00000512718.1:p.Val3CysfsTer?
ENST00000696561.1:c.6_7insT	ENSP00000512719.1:p.Val3CysfsTer?
ENST00000696562.1:c.6_7insT	ENSP00000512720.1:p.Val3CysfsTer?
ENST00000412585.7:c.6_7insT MANE Select	ENSP00000399168.2:p.Val3CysfsTer?
ENST00000412585.6:c.6_7insT	ENSP00000399168.2:p.Val3CysfsTer?
ENST00000434333.1:c.-90_-89insT	ENSP00000405931.1:n.-90_-89insT
ENST00000498007.1:n.27_28insT
ENST00000603274.1:n.506_507insA
NM_005514.6:c.6_7insT	NP_005505.2:p.Val3CysfsTer?
XM_011514557.1:c.6_7insT	XP_011512859.1:p.Val3CysfsTer?
XR_926175.1:n.16_17insT
NM_005514.7:c.6_7insT	NP_005505.2:p.Val3CysfsTer?
NM_005514.8:c.6_7insT MANE Select	NP_005505.2:p.Val3CysfsTer?