Canonical Allele Identifier: CA2770503821

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356440_31356441insT , CM000668.2:g.31356440_31356441insT	GRCh38
NC_000006.11:g.31324217_31324218insT , CM000668.1:g.31324217_31324218insT	GRCh37
NC_000006.10:g.31432196_31432197insT	NCBI36
NG_023187.1:g.5772_5773insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1818_1819insA
ENST00000481849.6:n.1818_1819insA
ENST00000497377.6:n.1818_1819insA
ENST00000640094.2:c.345_346insA	ENSP00000491275.2:p.Ser116IlefsTer23
ENST00000696558.1:c.345_346insA	ENSP00000512716.1:p.Ser116IlefsTer23
ENST00000696559.1:c.345_346insA	ENSP00000512717.1:p.Ser116IlefsTer23
ENST00000696560.1:c.345_346insA	ENSP00000512718.1:p.Ser116IlefsTer23
ENST00000696561.1:c.345_346insA	ENSP00000512719.1:p.Ser116IlefsTer23
ENST00000696562.1:c.345_346insA	ENSP00000512720.1:p.Ser116IlefsTer23
ENST00000412585.7:c.345_346insA MANE Select	ENSP00000399168.2:p.Ser116IlefsTer23
ENST00000412585.6:c.345_346insA	ENSP00000399168.2:p.Ser116IlefsTer23
ENST00000434333.1:c.378_379insA	ENSP00000405931.1:p.Ser127IlefsTer23
ENST00000474381.1:n.220_221insA
ENST00000498007.1:n.611_612insA
NM_005514.6:c.345_346insA	NP_005505.2:p.Ser116IlefsTer23
XM_011514556.1:c.378_379insA	XP_011512858.1:p.Ser127IlefsTer23
XM_011514557.1:c.345_346insA	XP_011512859.1:p.Ser116IlefsTer23
XR_926175.1:n.355_356insA
NM_005514.7:c.345_346insA	NP_005505.2:p.Ser116IlefsTer23
NM_005514.8:c.345_346insA MANE Select	NP_005505.2:p.Ser116IlefsTer23