Canonical Allele Identifier: CA1087469644

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356771-T-TC
• gnomAD v4: 6-31356771-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356771_31356772insC , CM000668.2:g.31356771_31356772insC	GRCh38
NC_000006.11:g.31324548_31324549insC , CM000668.1:g.31324548_31324549insC	GRCh37
NC_000006.10:g.31432527_31432528insC	NCBI36
NG_023187.1:g.5441_5442insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1732_1733insG
ENST00000481849.6:n.1732_1733insG
ENST00000497377.6:n.1732_1733insG
ENST00000640094.2:c.259_260insG	ENSP00000491275.2:p.Asn87ArgfsTer12
ENST00000696558.1:c.259_260insG	ENSP00000512716.1:p.Asn87ArgfsTer12
ENST00000696559.1:c.259_260insG	ENSP00000512717.1:p.Asn87ArgfsTer12
ENST00000696560.1:c.259_260insG	ENSP00000512718.1:p.Asn87ArgfsTer12
ENST00000696561.1:c.259_260insG	ENSP00000512719.1:p.Asn87ArgfsTer12
ENST00000696562.1:c.259_260insG	ENSP00000512720.1:p.Asn87ArgfsTer12
ENST00000412585.7:c.259_260insG MANE Select	ENSP00000399168.2:p.Asn87ArgfsTer12
ENST00000412585.6:c.259_260insG	ENSP00000399168.2:p.Asn87ArgfsTer12
ENST00000434333.1:c.292_293insG	ENSP00000405931.1:p.Asn98ArgfsTer12
ENST00000474381.1:n.134_135insG
ENST00000498007.1:n.280_281insG
ENST00000603274.1:n.125_126insC
NM_005514.6:c.259_260insG	NP_005505.2:p.Asn87ArgfsTer12
XM_011514556.1:c.292_293insG	XP_011512858.1:p.Asn98ArgfsTer12
XM_011514557.1:c.259_260insG	XP_011512859.1:p.Asn87ArgfsTer12
XR_926175.1:n.269_270insG
NM_005514.7:c.259_260insG	NP_005505.2:p.Asn87ArgfsTer12
NM_005514.8:c.259_260insG MANE Select	NP_005505.2:p.Asn87ArgfsTer12