Canonical Allele Identifier: CA1619112126

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356430_31356432delinsAGG , CM000668.2:g.31356430_31356432delinsAGG	GRCh38
NC_000006.11:g.31324207_31324209delinsAGG , CM000668.1:g.31324207_31324209delinsAGG	GRCh37
NC_000006.10:g.31432186_31432188delinsAGG	NCBI36
NG_023187.1:g.5781_5783delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1827_1829delinsCCT
ENST00000481849.6:n.1827_1829delinsCCT
ENST00000497377.6:n.1827_1829delinsCCT
ENST00000640094.2:c.354_356delinsCCT	ENSP00000491275.2:p.Thr118=
ENST00000696558.1:c.354_356delinsCCT	ENSP00000512716.1:p.Thr118=
ENST00000696559.1:c.354_356delinsCCT	ENSP00000512717.1:p.Thr118=
ENST00000696560.1:c.354_356delinsCCT	ENSP00000512718.1:p.Thr118=
ENST00000696561.1:c.354_356delinsCCT	ENSP00000512719.1:p.Thr118=
ENST00000696562.1:c.354_356delinsCCT	ENSP00000512720.1:p.Thr118=
ENST00000412585.7:c.354_356delinsCCT MANE Select	ENSP00000399168.2:p.Thr118=
ENST00000412585.6:c.354_356delinsCCT	ENSP00000399168.2:p.Thr118=
ENST00000434333.1:c.387_389delinsCCT	ENSP00000405931.1:p.Thr129=
ENST00000474381.1:n.229_231delinsCCT
ENST00000498007.1:n.620_622delinsCCT
NM_005514.6:c.354_356delinsCCT	NP_005505.2:p.Thr118=
XM_011514556.1:c.387_389delinsCCT	XP_011512858.1:p.Thr129=
XM_011514557.1:c.354_356delinsCCT	XP_011512859.1:p.Thr118=
XR_926175.1:n.364_366delinsCCT
NM_005514.7:c.354_356delinsCCT	NP_005505.2:p.Thr118=
NM_005514.8:c.354_356delinsCCT MANE Select	NP_005505.2:p.Thr118=