Canonical Allele Identifier: CA2515366310

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355094_31355095insTC , CM000668.2:g.31355094_31355095insTC	GRCh38
NC_000006.11:g.31322871_31322872insTC , CM000668.1:g.31322871_31322872insTC	GRCh37
NC_000006.10:g.31430850_31430851insTC	NCBI36
NG_023187.1:g.7118_7119insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+12_3059+13insGA
ENST00000481849.6:n.2590_2591insGA
ENST00000497377.6:n.2497_2498insGA
ENST00000640094.2:c.895+222_895+223insGA	ENSP00000491275.2:n.895+222_895+223insGA
ENST00000696558.1:c.1081+12_1081+13insGA	ENSP00000512716.1:n.1081+12_1081+13insGA
ENST00000696559.1:c.1012+12_1012+13insGA	ENSP00000512717.1:n.1012+12_1012+13insGA
ENST00000696560.1:c.1012+12_1012+13insGA	ENSP00000512718.1:n.1012+12_1012+13insGA
ENST00000696561.1:c.1012+12_1012+13insGA	ENSP00000512719.1:n.1012+12_1012+13insGA
ENST00000696562.1:c.1012+12_1012+13insGA	ENSP00000512720.1:n.1012+12_1012+13insGA
ENST00000412585.7:c.1012+12_1012+13insGA MANE Select	ENSP00000399168.2:n.1012+12_1012+13insGA
ENST00000640094.1:c.88+222_88+223insGA	ENSP00000491275.1:n.88+222_88+223insGA
ENST00000412585.6:c.1012+12_1012+13insGA	ENSP00000399168.2:n.1012+12_1012+13insGA
NM_005514.6:c.1012+12_1012+13insGA	NP_005505.2:n.1012+12_1012+13insGA
XM_011514556.1:c.1045+12_1045+13insGA	XP_011512858.1:n.1045+12_1045+13insGA
XM_011514557.1:c.895+222_895+223insGA	XP_011512859.1:n.895+222_895+223insGA
XR_926175.1:n.1451+12_1451+13insGA
NM_005514.7:c.1012+12_1012+13insGA	NP_005505.2:n.1012+12_1012+13insGA
NM_005514.8:c.1012+12_1012+13insGA MANE Select	NP_005505.2:n.1012+12_1012+13insGA