Canonical Allele Identifier: CA2677953791

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354425-C-CCCCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354427_31354428insCTTCC , CM000668.2:g.31354427_31354428insCTTCC	GRCh38
NC_000006.11:g.31322204_31322205insCTTCC , CM000668.1:g.31322204_31322205insCTTCC	GRCh37
NC_000006.10:g.31430183_31430184insCTTCC	NCBI36
NG_023187.1:g.7787_7788insAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+53_3140+54insAAGGG
ENST00000481849.6:n.3100+53_3100+54insAAGGG
ENST00000497377.6:n.3007+53_3007+54insAAGGG
ENST00000696558.1:c.1162+53_1162+54insAAGGG	ENSP00000512716.1:n.1162+53_1162+54insAAGGG
ENST00000696559.1:c.*4+53_*4+54insAAGGG	ENSP00000512717.1:n.*4+53_*4+54insAAGGG
ENST00000696560.1:c.*4+53_*4+54insAAGGG	ENSP00000512718.1:n.*4+53_*4+54insAAGGG
ENST00000696561.1:c.*4+53_*4+54insAAGGG	ENSP00000512719.1:n.*4+53_*4+54insAAGGG
ENST00000696562.1:c.*4+53_*4+54insAAGGG	ENSP00000512720.1:n.*4+53_*4+54insAAGGG
ENST00000412585.7:c.*4+53_*4+54insAAGGG MANE Select	ENSP00000399168.2:n.*4+53_*4+54insAAGGG
ENST00000412585.6:c.*4+53_*4+54insAAGGG	ENSP00000399168.2:n.*4+53_*4+54insAAGGG
ENST00000481849.5:n.328+53_328+54insAAGGG
ENST00000497377.5:n.492+53_492+54insAAGGG
NM_005514.6:c.*4+53_*4+54insAAGGG	NP_005505.2:n.*4+53_*4+54insAAGGG
XM_011514556.1:c.*4+53_*4+54insAAGGG	XP_011512858.1:n.*4+53_*4+54insAAGGG
XM_011514557.1:c.*4+53_*4+54insAAGGG	XP_011512859.1:n.*4+53_*4+54insAAGGG
XR_926175.1:n.1532+53_1532+54insAAGGG
NM_005514.7:c.*4+53_*4+54insAAGGG	NP_005505.2:n.*4+53_*4+54insAAGGG
NM_005514.8:c.*4+53_*4+54insAAGGG MANE Select	NP_005505.2:n.*4+53_*4+54insAAGGG