Canonical Allele Identifier: CA1938907776

Gene: HSPA12A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.116816574G= , CM000672.2:g.116816574G=	GRCh38
NC_000010.10:g.118576085G= , CM000672.1:g.118576085G=	GRCh37
NC_000010.9:g.118566075G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635765.1:c.91+18361C=	ENSP00000489674.1:n.91+18361C=
ENST00000674167.1:c.-124+18361C=	ENSP00000501417.1:n.-124+18361C=
ENST00000674197.1:c.88+18361C=	ENSP00000501472.1:n.88+18361C=
ENST00000674401.1:c.-210+32992C=	ENSP00000501414.1:n.-210+32992C=
ENST00000674505.1:c.-210+32992C=	ENSP00000501396.1:n.-210+32992C=
XM_005269672.2:c.91+18361C=	XP_005269729.1:n.91+18361C=
XM_005269673.3:c.88+18361C=	XP_005269730.1:n.88+18361C=
XM_011539579.1:c.88+18361C=	XP_011537881.1:n.88+18361C=
NM_001330164.1:c.91+18361C=	NP_001317093.1:n.91+18361C=
XM_005269673.5:c.88+18361C=	XP_005269730.1:n.88+18361C=
XM_011539579.2:c.88+18361C=	XP_011537881.1:n.88+18361C=
NM_001330164.2:c.91+18361C=	NP_001317093.1:n.91+18361C=