Canonical Allele Identifier: CA932930135

Gene: HSPA12A

Linked Data

• dbSNP Id: rs1845311703
• gnomAD v3: 10-116816646-C-T
• gnomAD v4: 10-116816646-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.116816646C>T , CM000672.2:g.116816646C>T	GRCh38
NC_000010.10:g.118576157C>T , CM000672.1:g.118576157C>T	GRCh37
NC_000010.9:g.118566147C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635765.1:c.91+18289G>A	ENSP00000489674.1:n.91+18289G>A
ENST00000674167.1:c.-124+18289G>A	ENSP00000501417.1:n.-124+18289G>A
ENST00000674197.1:c.88+18289G>A	ENSP00000501472.1:n.88+18289G>A
ENST00000674401.1:c.-210+32920G>A	ENSP00000501414.1:n.-210+32920G>A
ENST00000674505.1:c.-210+32920G>A	ENSP00000501396.1:n.-210+32920G>A
XM_005269672.2:c.91+18289G>A	XP_005269729.1:n.91+18289G>A
XM_005269673.3:c.88+18289G>A	XP_005269730.1:n.88+18289G>A
XM_011539579.1:c.88+18289G>A	XP_011537881.1:n.88+18289G>A
NM_001330164.1:c.91+18289G>A	NP_001317093.1:n.91+18289G>A
XM_005269673.5:c.88+18289G>A	XP_005269730.1:n.88+18289G>A
XM_011539579.2:c.88+18289G>A	XP_011537881.1:n.88+18289G>A
NM_001330164.2:c.91+18289G>A	NP_001317093.1:n.91+18289G>A