Canonical Allele Identifier: CA1087464653

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355156-C-CTAGG
• gnomAD v4: 6-31355156-C-CTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355156_31355157insTAGG , CM000668.2:g.31355156_31355157insTAGG	GRCh38
NC_000006.11:g.31322933_31322934insTAGG , CM000668.1:g.31322933_31322934insTAGG	GRCh37
NC_000006.10:g.31430912_31430913insTAGG	NCBI36
NG_023187.1:g.7056_7057insCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3009_3010insCCTA
ENST00000481849.6:n.2528_2529insCCTA
ENST00000497377.6:n.2435_2436insCCTA
ENST00000640094.2:c.895+160_895+161insCCTA	ENSP00000491275.2:n.895+160_895+161insCCTA
ENST00000696558.1:c.1031_1032insCCTA	ENSP00000512716.1:n.1031_1032insCCTA
ENST00000696559.1:c.962_963insCCTA	ENSP00000512717.1:p.Val322LeufsTer13
ENST00000696560.1:c.962_963insCCTA	ENSP00000512718.1:p.Val322LeufsTer13
ENST00000696561.1:c.962_963insCCTA	ENSP00000512719.1:p.Val322LeufsTer13
ENST00000696562.1:c.962_963insCCTA	ENSP00000512720.1:p.Val322LeufsTer13
ENST00000412585.7:c.962_963insCCTA MANE Select	ENSP00000399168.2:p.Val322LeufsTer13
ENST00000640094.1:c.88+160_88+161insCCTA	ENSP00000491275.1:n.88+160_88+161insCCTA
ENST00000412585.6:c.962_963insCCTA	ENSP00000399168.2:p.Val322LeufsTer13
ENST00000463574.1:n.553_554insCCTA
NM_005514.6:c.962_963insCCTA	NP_005505.2:p.Val322LeufsTer13
XM_011514556.1:c.995_996insCCTA	XP_011512858.1:p.Val333LeufsTer13
XM_011514557.1:c.895+160_895+161insCCTA	XP_011512859.1:n.895+160_895+161insCCTA
XR_926175.1:n.1401_1402insCCTA
NM_005514.7:c.962_963insCCTA	NP_005505.2:p.Val322LeufsTer13
NM_005514.8:c.962_963insCCTA MANE Select	NP_005505.2:p.Val322LeufsTer13