Canonical Allele Identifier: CA2770503807

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356377_31356378insTA , CM000668.2:g.31356377_31356378insTA	GRCh38
NC_000006.11:g.31324154_31324155insTA , CM000668.1:g.31324154_31324155insTA	GRCh37
NC_000006.10:g.31432133_31432134insTA	NCBI36
NG_023187.1:g.5835_5836insTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1881_1882insTA
ENST00000481849.6:n.1881_1882insTA
ENST00000497377.6:n.1881_1882insTA
ENST00000640094.2:c.408_409insTA	ENSP00000491275.2:p.His137TyrfsTer15
ENST00000696558.1:c.408_409insTA	ENSP00000512716.1:p.His137TyrfsTer15
ENST00000696559.1:c.408_409insTA	ENSP00000512717.1:p.His137TyrfsTer15
ENST00000696560.1:c.408_409insTA	ENSP00000512718.1:p.His137TyrfsTer15
ENST00000696561.1:c.408_409insTA	ENSP00000512719.1:p.His137TyrfsTer15
ENST00000696562.1:c.408_409insTA	ENSP00000512720.1:p.His137TyrfsTer15
ENST00000412585.7:c.408_409insTA MANE Select	ENSP00000399168.2:p.His137TyrfsTer15
ENST00000412585.6:c.408_409insTA	ENSP00000399168.2:p.His137TyrfsTer15
ENST00000434333.1:c.441_442insTA	ENSP00000405931.1:p.His148TyrfsTer15
ENST00000474381.1:n.283_284insTA
ENST00000498007.1:n.674_675insTA
NM_005514.6:c.408_409insTA	NP_005505.2:p.His137TyrfsTer15
XM_011514556.1:c.441_442insTA	XP_011512858.1:p.His148TyrfsTer15
XM_011514557.1:c.408_409insTA	XP_011512859.1:p.His137TyrfsTer15
XR_926175.1:n.418_419insTA
NM_005514.7:c.408_409insTA	NP_005505.2:p.His137TyrfsTer15
NM_005514.8:c.408_409insTA MANE Select	NP_005505.2:p.His137TyrfsTer15