Canonical Allele Identifier: CA625104254

Gene: ALDH3A2

Linked Data

• dbSNP Id: rs1261365038
• gnomAD v2: 17-19552055-G-A
• gnomAD v3: 17-19648742-G-A
• gnomAD v4: 17-19648742-G-A
• MyVariant Identifiers: chr17:g.19552055G>A (hg19) ; chr17:g.19648742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19648742G>A , CM000679.2:g.19648742G>A	GRCh38
NC_000017.10:g.19552055G>A , CM000679.1:g.19552055G>A	GRCh37
NC_000017.9:g.19492647G>A	NCBI36
NG_007095.2:g.4992G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467473.6:n.87-193G>A
ENST00000581518.6:c.-37-193G>A	ENSP00000461916.2:n.-37-193G>A
ENST00000672357.1:c.-139G>A	ENSP00000500092.1:n.-139G>A
ENST00000672465.1:c.-37-193G>A	ENSP00000500517.1:n.-37-193G>A
ENST00000673136.1:c.-37-193G>A	ENSP00000500380.1:n.-37-193G>A
ENST00000176643.10:c.-230G>A	ENSP00000176643.6:n.-230G>A
ENST00000395575.6:c.-139G>A	ENSP00000378942.2:n.-139G>A
ENST00000446398.6:c.-37-193G>A	ENSP00000395845.2:n.-37-193G>A
ENST00000467473.5:n.121-193G>A
ENST00000580550.5:c.-9-221G>A	ENSP00000462964.1:n.-9-221G>A
ENST00000581518.5:c.-230G>A	ENSP00000461916.1:n.-230G>A
ENST00000582991.5:c.-230G>A	ENSP00000464153.1:n.-230G>A
ENST00000626500.2:c.-230G>A	ENSP00000486283.1:n.-230G>A
ENST00000631291.2:c.-230G>A	ENSP00000486085.1:n.-230G>A
XM_011523733.1:c.-37-193G>A	XP_011522035.1:n.-37-193G>A
XM_011523733.2:c.-37-193G>A	XP_011522035.1:n.-37-193G>A
XM_017024356.2:c.-37-193G>A	XP_016879845.1:n.-37-193G>A
XM_017024358.2:c.-37-193G>A	XP_016879847.1:n.-37-193G>A
XM_024450652.1:c.-725-193G>A	XP_024306420.1:n.-725-193G>A
NM_001369137.1:c.-37-193G>A	NP_001356066.1:n.-37-193G>A
NM_001369138.1:c.-37-193G>A	NP_001356067.1:n.-37-193G>A
NM_001369146.1:c.-37-193G>A	NP_001356075.1:n.-37-193G>A
NM_001369148.1:c.-725-193G>A	NP_001356077.1:n.-725-193G>A
NM_001369137.2:c.-37-193G>A	NP_001356066.1:n.-37-193G>A
NM_001369138.2:c.-37-193G>A	NP_001356067.1:n.-37-193G>A
NM_001369146.2:c.-37-193G>A	NP_001356075.1:n.-37-193G>A
NM_001369148.2:c.-725-193G>A	NP_001356077.1:n.-725-193G>A