Canonical Allele Identifier: CA2564581111

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354430-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354430_31354431insAT , CM000668.2:g.31354430_31354431insAT	GRCh38
NC_000006.11:g.31322207_31322208insAT , CM000668.1:g.31322207_31322208insAT	GRCh37
NC_000006.10:g.31430186_31430187insAT	NCBI36
NG_023187.1:g.7782_7783insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+48_3140+49insAT
ENST00000481849.6:n.3100+48_3100+49insAT
ENST00000497377.6:n.3007+48_3007+49insAT
ENST00000696558.1:c.1162+48_1162+49insAT	ENSP00000512716.1:n.1162+48_1162+49insAT
ENST00000696559.1:c.*4+48_*4+49insAT	ENSP00000512717.1:n.*4+48_*4+49insAT
ENST00000696560.1:c.*4+48_*4+49insAT	ENSP00000512718.1:n.*4+48_*4+49insAT
ENST00000696561.1:c.*4+48_*4+49insAT	ENSP00000512719.1:n.*4+48_*4+49insAT
ENST00000696562.1:c.*4+48_*4+49insAT	ENSP00000512720.1:n.*4+48_*4+49insAT
ENST00000412585.7:c.*4+48_*4+49insAT MANE Select	ENSP00000399168.2:n.*4+48_*4+49insAT
ENST00000412585.6:c.*4+48_*4+49insAT	ENSP00000399168.2:n.*4+48_*4+49insAT
ENST00000481849.5:n.328+48_328+49insAT
ENST00000497377.5:n.492+48_492+49insAT
NM_005514.6:c.*4+48_*4+49insAT	NP_005505.2:n.*4+48_*4+49insAT
XM_011514556.1:c.*4+48_*4+49insAT	XP_011512858.1:n.*4+48_*4+49insAT
XM_011514557.1:c.*4+48_*4+49insAT	XP_011512859.1:n.*4+48_*4+49insAT
XR_926175.1:n.1532+48_1532+49insAT
NM_005514.7:c.*4+48_*4+49insAT	NP_005505.2:n.*4+48_*4+49insAT
NM_005514.8:c.*4+48_*4+49insAT MANE Select	NP_005505.2:n.*4+48_*4+49insAT