Canonical Allele Identifier: CA214930790

Gene: HSPA12A

Linked Data

• dbSNP Id: rs559326839
• gnomAD v3: 10-116816551-A-G
• gnomAD v4: 10-116816551-A-G
• MyVariant Identifiers: chr10:g.118576062A>G (hg19) ; chr10:g.116816551A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.116816551A>G , CM000672.2:g.116816551A>G	GRCh38
NC_000010.10:g.118576062A>G , CM000672.1:g.118576062A>G	GRCh37
NC_000010.9:g.118566052A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635765.1:c.91+18384T>C	ENSP00000489674.1:n.91+18384T>C
ENST00000674167.1:c.-124+18384T>C	ENSP00000501417.1:n.-124+18384T>C
ENST00000674197.1:c.88+18384T>C	ENSP00000501472.1:n.88+18384T>C
ENST00000674401.1:c.-210+33015T>C	ENSP00000501414.1:n.-210+33015T>C
ENST00000674505.1:c.-210+33015T>C	ENSP00000501396.1:n.-210+33015T>C
XM_005269672.2:c.91+18384T>C	XP_005269729.1:n.91+18384T>C
XM_005269673.3:c.88+18384T>C	XP_005269730.1:n.88+18384T>C
XM_011539579.1:c.88+18384T>C	XP_011537881.1:n.88+18384T>C
NM_001330164.1:c.91+18384T>C	NP_001317093.1:n.91+18384T>C
XM_005269673.5:c.88+18384T>C	XP_005269730.1:n.88+18384T>C
XM_011539579.2:c.88+18384T>C	XP_011537881.1:n.88+18384T>C
NM_001330164.2:c.91+18384T>C	NP_001317093.1:n.91+18384T>C