Canonical Allele Identifier: CA650785948

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355094-A-AT
• COSMIC: COSN2534181 ; COSN2534660

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355094_31355095insT , CM000668.2:g.31355094_31355095insT	GRCh38
NC_000006.11:g.31322871_31322872insT , CM000668.1:g.31322871_31322872insT	GRCh37
NC_000006.10:g.31430850_31430851insT	NCBI36
NG_023187.1:g.7118_7119insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+12_3059+13insA
ENST00000481849.6:n.2590_2591insA
ENST00000497377.6:n.2497_2498insA
ENST00000640094.2:c.895+222_895+223insA	ENSP00000491275.2:n.895+222_895+223insA
ENST00000696558.1:c.1081+12_1081+13insA	ENSP00000512716.1:n.1081+12_1081+13insA
ENST00000696559.1:c.1012+12_1012+13insA	ENSP00000512717.1:n.1012+12_1012+13insA
ENST00000696560.1:c.1012+12_1012+13insA	ENSP00000512718.1:n.1012+12_1012+13insA
ENST00000696561.1:c.1012+12_1012+13insA	ENSP00000512719.1:n.1012+12_1012+13insA
ENST00000696562.1:c.1012+12_1012+13insA	ENSP00000512720.1:n.1012+12_1012+13insA
ENST00000412585.7:c.1012+12_1012+13insA MANE Select	ENSP00000399168.2:n.1012+12_1012+13insA
ENST00000640094.1:c.88+222_88+223insA	ENSP00000491275.1:n.88+222_88+223insA
ENST00000412585.6:c.1012+12_1012+13insA	ENSP00000399168.2:n.1012+12_1012+13insA
NM_005514.6:c.1012+12_1012+13insA	NP_005505.2:n.1012+12_1012+13insA
XM_011514556.1:c.1045+12_1045+13insA	XP_011512858.1:n.1045+12_1045+13insA
XM_011514557.1:c.895+222_895+223insA	XP_011512859.1:n.895+222_895+223insA
XR_926175.1:n.1451+12_1451+13insA
NM_005514.7:c.1012+12_1012+13insA	NP_005505.2:n.1012+12_1012+13insA
NM_005514.8:c.1012+12_1012+13insA MANE Select	NP_005505.2:n.1012+12_1012+13insA