Canonical Allele Identifier: CA2770503837

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356770_31356772delinsCTC , CM000668.2:g.31356770_31356772delinsCTC	GRCh38
NC_000006.11:g.31324547_31324549delinsCTC , CM000668.1:g.31324547_31324549delinsCTC	GRCh37
NC_000006.10:g.31432526_31432528delinsCTC	NCBI36
NG_023187.1:g.5441_5443delinsGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1732_1734delinsGAG
ENST00000481849.6:n.1732_1734delinsGAG
ENST00000497377.6:n.1732_1734delinsGAG
ENST00000640094.2:c.259_261delinsGAG	ENSP00000491275.2:p.Asn87Glu
ENST00000696558.1:c.259_261delinsGAG	ENSP00000512716.1:p.Asn87Glu
ENST00000696559.1:c.259_261delinsGAG	ENSP00000512717.1:p.Asn87Glu
ENST00000696560.1:c.259_261delinsGAG	ENSP00000512718.1:p.Asn87Glu
ENST00000696561.1:c.259_261delinsGAG	ENSP00000512719.1:p.Asn87Glu
ENST00000696562.1:c.259_261delinsGAG	ENSP00000512720.1:p.Asn87Glu
ENST00000412585.7:c.259_261delinsGAG MANE Select	ENSP00000399168.2:p.Asn87Glu
ENST00000412585.6:c.259_261delinsGAG	ENSP00000399168.2:p.Asn87Glu
ENST00000434333.1:c.292_294delinsGAG	ENSP00000405931.1:p.Asn98Glu
ENST00000474381.1:n.134_136delinsGAG
ENST00000498007.1:n.280_282delinsGAG
ENST00000603274.1:n.124_126delinsCTC
NM_005514.6:c.259_261delinsGAG	NP_005505.2:p.Asn87Glu
XM_011514556.1:c.292_294delinsGAG	XP_011512858.1:p.Asn98Glu
XM_011514557.1:c.259_261delinsGAG	XP_011512859.1:p.Asn87Glu
XR_926175.1:n.269_271delinsGAG
NM_005514.7:c.259_261delinsGAG	NP_005505.2:p.Asn87Glu
NM_005514.8:c.259_261delinsGAG MANE Select	NP_005505.2:p.Asn87Glu