Canonical Allele Identifier: CA2770503830

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356732_31356733insG , CM000668.2:g.31356732_31356733insG	GRCh38
NC_000006.11:g.31324509_31324510insG , CM000668.1:g.31324509_31324510insG	GRCh37
NC_000006.10:g.31432488_31432489insG	NCBI36
NG_023187.1:g.5480_5481insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1771_1772insC
ENST00000481849.6:n.1771_1772insC
ENST00000497377.6:n.1771_1772insC
ENST00000640094.2:c.298_299insC	ENSP00000491275.2:p.Glu100AlafsTer?
ENST00000696558.1:c.298_299insC	ENSP00000512716.1:p.Glu100AlafsTer?
ENST00000696559.1:c.298_299insC	ENSP00000512717.1:p.Glu100AlafsTer?
ENST00000696560.1:c.298_299insC	ENSP00000512718.1:p.Glu100AlafsTer?
ENST00000696561.1:c.298_299insC	ENSP00000512719.1:p.Glu100AlafsTer?
ENST00000696562.1:c.298_299insC	ENSP00000512720.1:p.Glu100AlafsTer?
ENST00000412585.7:c.298_299insC MANE Select	ENSP00000399168.2:p.Glu100AlafsTer?
ENST00000412585.6:c.298_299insC	ENSP00000399168.2:p.Glu100AlafsTer?
ENST00000434333.1:c.331_332insC	ENSP00000405931.1:p.Glu111AlafsTer?
ENST00000474381.1:n.173_174insC
ENST00000498007.1:n.319_320insC
ENST00000603274.1:n.86_87insG
NM_005514.6:c.298_299insC	NP_005505.2:p.Glu100AlafsTer?
XM_011514556.1:c.331_332insC	XP_011512858.1:p.Glu111AlafsTer?
XM_011514557.1:c.298_299insC	XP_011512859.1:p.Glu100AlafsTer?
XR_926175.1:n.308_309insC
NM_005514.7:c.298_299insC	NP_005505.2:p.Glu100AlafsTer?
NM_005514.8:c.298_299insC MANE Select	NP_005505.2:p.Glu100AlafsTer?