Canonical Allele Identifier: CA2677957909

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357118-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357118_31357119insC , CM000668.2:g.31357118_31357119insC	GRCh38
NC_000006.11:g.31324895_31324896insC , CM000668.1:g.31324895_31324896insC	GRCh37
NC_000006.10:g.31432874_31432875insC	NCBI36
NG_023187.1:g.5094_5095insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1513_1514insG
ENST00000481849.6:n.1513_1514insG
ENST00000497377.6:n.1513_1514insG
ENST00000640094.2:c.40_41insG	ENSP00000491275.2:p.Ser14CysfsTer?
ENST00000696558.1:c.40_41insG	ENSP00000512716.1:p.Ser14CysfsTer?
ENST00000696559.1:c.40_41insG	ENSP00000512717.1:p.Ser14CysfsTer?
ENST00000696560.1:c.40_41insG	ENSP00000512718.1:p.Ser14CysfsTer?
ENST00000696561.1:c.40_41insG	ENSP00000512719.1:p.Ser14CysfsTer?
ENST00000696562.1:c.40_41insG	ENSP00000512720.1:p.Ser14CysfsTer?
ENST00000412585.7:c.40_41insG MANE Select	ENSP00000399168.2:p.Ser14CysfsTer?
ENST00000412585.6:c.40_41insG	ENSP00000399168.2:p.Ser14CysfsTer?
ENST00000434333.1:c.-56_-55insG	ENSP00000405931.1:n.-56_-55insG
ENST00000498007.1:n.61_62insG
ENST00000603274.1:n.472_473insC
NM_005514.6:c.40_41insG	NP_005505.2:p.Ser14CysfsTer?
XM_011514557.1:c.40_41insG	XP_011512859.1:p.Ser14CysfsTer?
XR_926175.1:n.50_51insG
NM_005514.7:c.40_41insG	NP_005505.2:p.Ser14CysfsTer?
NM_005514.8:c.40_41insG MANE Select	NP_005505.2:p.Ser14CysfsTer?