Canonical Allele Identifier: CA1938907831

Gene: HSPA12A

Linked Data

• dbSNP Id: rs1564829211

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.116816672C>G , CM000672.2:g.116816672C>G	GRCh38
NC_000010.10:g.118576183C>G , CM000672.1:g.118576183C>G	GRCh37
NC_000010.9:g.118566173C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635765.1:c.91+18263G>C	ENSP00000489674.1:n.91+18263G>C
ENST00000674167.1:c.-124+18263G>C	ENSP00000501417.1:n.-124+18263G>C
ENST00000674197.1:c.88+18263G>C	ENSP00000501472.1:n.88+18263G>C
ENST00000674401.1:c.-210+32894G>C	ENSP00000501414.1:n.-210+32894G>C
ENST00000674505.1:c.-210+32894G>C	ENSP00000501396.1:n.-210+32894G>C
XM_005269672.2:c.91+18263G>C	XP_005269729.1:n.91+18263G>C
XM_005269673.3:c.88+18263G>C	XP_005269730.1:n.88+18263G>C
XM_011539579.1:c.88+18263G>C	XP_011537881.1:n.88+18263G>C
NM_001330164.1:c.91+18263G>C	NP_001317093.1:n.91+18263G>C
XM_005269673.5:c.88+18263G>C	XP_005269730.1:n.88+18263G>C
XM_011539579.2:c.88+18263G>C	XP_011537881.1:n.88+18263G>C
NM_001330164.2:c.91+18263G>C	NP_001317093.1:n.91+18263G>C