Canonical Allele Identifier: CA2770503838

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356775_31356776insCCCC , CM000668.2:g.31356775_31356776insCCCC	GRCh38
NC_000006.11:g.31324552_31324553insCCCC , CM000668.1:g.31324552_31324553insCCCC	GRCh37
NC_000006.10:g.31432531_31432532insCCCC	NCBI36
NG_023187.1:g.5437_5438insGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1728_1729insGGGG
ENST00000481849.6:n.1728_1729insGGGG
ENST00000497377.6:n.1728_1729insGGGG
ENST00000640094.2:c.255_256insGGGG	ENSP00000491275.2:p.Arg86GlyfsTer14
ENST00000696558.1:c.255_256insGGGG	ENSP00000512716.1:p.Arg86GlyfsTer14
ENST00000696559.1:c.255_256insGGGG	ENSP00000512717.1:p.Arg86GlyfsTer14
ENST00000696560.1:c.255_256insGGGG	ENSP00000512718.1:p.Arg86GlyfsTer14
ENST00000696561.1:c.255_256insGGGG	ENSP00000512719.1:p.Arg86GlyfsTer14
ENST00000696562.1:c.255_256insGGGG	ENSP00000512720.1:p.Arg86GlyfsTer14
ENST00000412585.7:c.255_256insGGGG MANE Select	ENSP00000399168.2:p.Arg86GlyfsTer14
ENST00000412585.6:c.255_256insGGGG	ENSP00000399168.2:p.Arg86GlyfsTer14
ENST00000434333.1:c.288_289insGGGG	ENSP00000405931.1:p.Arg97GlyfsTer14
ENST00000474381.1:n.130_131insGGGG
ENST00000498007.1:n.276_277insGGGG
ENST00000603274.1:n.129_130insCCCC
NM_005514.6:c.255_256insGGGG	NP_005505.2:p.Arg86GlyfsTer14
XM_011514556.1:c.288_289insGGGG	XP_011512858.1:p.Arg97GlyfsTer14
XM_011514557.1:c.255_256insGGGG	XP_011512859.1:p.Arg86GlyfsTer14
XR_926175.1:n.265_266insGGGG
NM_005514.7:c.255_256insGGGG	NP_005505.2:p.Arg86GlyfsTer14
NM_005514.8:c.255_256insGGGG MANE Select	NP_005505.2:p.Arg86GlyfsTer14