Canonical Allele Identifier: CA288537088

Gene: ALDH3A2

Linked Data

• dbSNP Id: rs1030689155
• gnomAD v4: 17-19648778-A-G
• MyVariant Identifiers: chr17:g.19552091A>G (hg19) ; chr17:g.19648778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19648778A>G , CM000679.2:g.19648778A>G	GRCh38
NC_000017.10:g.19552091A>G , CM000679.1:g.19552091A>G	GRCh37
NC_000017.9:g.19492683A>G	NCBI36
NG_007095.2:g.5028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.-194A>G MANE Select	ENSP00000176643.6:n.-194A>G
ENST00000467473.6:n.87-157A>G
ENST00000581518.6:c.-37-157A>G	ENSP00000461916.2:n.-37-157A>G
ENST00000672357.1:c.-103A>G	ENSP00000500092.1:n.-103A>G
ENST00000672465.1:c.-37-157A>G	ENSP00000500517.1:n.-37-157A>G
ENST00000672564.1:n.28A>G
ENST00000673136.1:c.-37-157A>G	ENSP00000500380.1:n.-37-157A>G
ENST00000176643.10:c.-194A>G	ENSP00000176643.6:n.-194A>G
ENST00000339618.8:c.-194A>G	ENSP00000345774.4:n.-194A>G
ENST00000395575.6:c.-103A>G	ENSP00000378942.2:n.-103A>G
ENST00000446398.6:c.-37-157A>G	ENSP00000395845.2:n.-37-157A>G
ENST00000467473.5:n.121-157A>G
ENST00000578614.1:c.-194A>G	ENSP00000463128.1:n.-194A>G
ENST00000579855.5:c.-72A>G	ENSP00000463637.1:n.-72A>G
ENST00000580550.5:c.-9-185A>G	ENSP00000462964.1:n.-9-185A>G
ENST00000581518.5:c.-194A>G	ENSP00000461916.1:n.-194A>G
ENST00000582991.5:c.-194A>G	ENSP00000464153.1:n.-194A>G
ENST00000584332.6:c.-166A>G	ENSP00000466814.1:n.-166A>G
ENST00000626500.2:c.-194A>G	ENSP00000486283.1:n.-194A>G
ENST00000631291.2:c.-194A>G	ENSP00000486085.1:n.-194A>G
NM_000382.2:c.-194A>G	NP_000373.1:n.-194A>G
NM_001031806.1:c.-194A>G	NP_001026976.1:n.-194A>G
XM_011523732.1:c.-103A>G	XP_011522034.1:n.-103A>G
XM_011523733.1:c.-37-157A>G	XP_011522035.1:n.-37-157A>G
XM_011523733.2:c.-37-157A>G	XP_011522035.1:n.-37-157A>G
XM_017024356.2:c.-37-157A>G	XP_016879845.1:n.-37-157A>G
XM_017024357.1:c.-103A>G	XP_016879846.1:n.-103A>G
XM_017024358.2:c.-37-157A>G	XP_016879847.1:n.-37-157A>G
XM_024450652.1:c.-725-157A>G	XP_024306420.1:n.-725-157A>G
NM_000382.3:c.-194A>G MANE Select	NP_000373.1:n.-194A>G
NM_001031806.2:c.-194A>G	NP_001026976.1:n.-194A>G
NM_001369136.1:c.-103A>G	NP_001356065.1:n.-103A>G
NM_001369137.1:c.-37-157A>G	NP_001356066.1:n.-37-157A>G
NM_001369138.1:c.-37-157A>G	NP_001356067.1:n.-37-157A>G
NM_001369139.1:c.-103A>G	NP_001356068.1:n.-103A>G
NM_001369146.1:c.-37-157A>G	NP_001356075.1:n.-37-157A>G
NM_001369148.1:c.-725-157A>G	NP_001356077.1:n.-725-157A>G
NM_001369137.2:c.-37-157A>G	NP_001356066.1:n.-37-157A>G
NM_001369138.2:c.-37-157A>G	NP_001356067.1:n.-37-157A>G
NM_001369146.2:c.-37-157A>G	NP_001356075.1:n.-37-157A>G
NM_001369148.2:c.-725-157A>G	NP_001356077.1:n.-725-157A>G