Canonical Allele Identifier: CA398709068

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19564458A>G (hg19) ; chr17:g.19661145A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19661145A>G , CM000679.2:g.19661145A>G	GRCh38
NC_000017.10:g.19564458A>G , CM000679.1:g.19564458A>G	GRCh37
NC_000017.9:g.19505050A>G	NCBI36
NG_007095.2:g.17395A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.817A>G MANE Select	ENSP00000176643.6:p.Ile273Val
ENST00000395575.7:c.490A>G	ENSP00000378942.3:p.Ile164Val
ENST00000472059.6:c.*375A>G	ENSP00000458397.1:n.*375A>G
ENST00000574078.3:n.146A>G
ENST00000581518.6:c.817A>G	ENSP00000461916.2:p.Ile273Val
ENST00000582991.6:c.817A>G	ENSP00000464153.1:p.Ile273Val
ENST00000671841.1:n.2496A>G
ENST00000671878.1:c.817A>G	ENSP00000500516.1:p.Ile273Val
ENST00000672059.1:n.1268A>G
ENST00000672357.1:c.817A>G	ENSP00000500092.1:p.Ile273Val
ENST00000672465.1:c.817A>G	ENSP00000500517.1:p.Ile273Val
ENST00000672487.1:c.699A>G	ENSP00000500740.1:p.Ile233Met
ENST00000672564.1:n.1038A>G
ENST00000672567.1:c.708A>G
ENST00000672608.1:n.1806A>G
ENST00000672709.1:c.671A>G
ENST00000673064.1:n.1317A>G
ENST00000673136.1:c.817A>G	ENSP00000500380.1:p.Ile273Val
ENST00000673472.1:n.1153A>G
ENST00000673516.1:n.1277A>G
ENST00000176643.10:c.817A>G	ENSP00000176643.6:p.Ile273Val
ENST00000339618.8:c.817A>G	ENSP00000345774.4:p.Ile273Val
ENST00000395575.6:c.817A>G	ENSP00000378942.2:p.Ile273Val
ENST00000472059.5:c.*375A>G	ENSP00000458397.1:n.*375A>G
ENST00000476965.5:n.567A>G
ENST00000571537.1:c.310A>G	ENSP00000458942.1:p.Ile104Val
ENST00000574078.2:n.146A>G
ENST00000578696.1:c.248A>G
ENST00000579855.5:c.817A>G	ENSP00000463637.1:p.Ile273Val
ENST00000581518.5:c.817A>G	ENSP00000461916.1:p.Ile273Val
ENST00000582991.5:c.817A>G	ENSP00000464153.1:p.Ile273Val
ENST00000630662.2:c.-165A>G	ENSP00000487353.1:n.-165A>G
ENST00000631291.2:c.817A>G	ENSP00000486085.1:p.Ile273Val
NM_000382.2:c.817A>G	NP_000373.1:p.Ile273Val
NM_001031806.1:c.817A>G	NP_001026976.1:p.Ile273Val
XM_011523732.1:c.817A>G	XP_011522034.1:p.Ile273Val
XM_011523733.1:c.817A>G	XP_011522035.1:p.Ile273Val
XM_011523733.2:c.817A>G	XP_011522035.1:p.Ile273Val
XM_017024355.1:c.817A>G	XP_016879844.1:p.Ile273Val
XM_017024356.2:c.817A>G	XP_016879845.1:p.Ile273Val
XM_017024357.1:c.817A>G	XP_016879846.1:p.Ile273Val
XM_017024358.2:c.817A>G	XP_016879847.1:p.Ile273Val
XM_024450651.1:c.238A>G	XP_024306419.1:p.Ile80Val
XM_024450652.1:c.238A>G	XP_024306420.1:p.Ile80Val
NM_000382.3:c.817A>G MANE Select	NP_000373.1:p.Ile273Val
NM_001031806.2:c.817A>G	NP_001026976.1:p.Ile273Val
NM_001369136.1:c.817A>G	NP_001356065.1:p.Ile273Val
NM_001369137.1:c.817A>G	NP_001356066.1:p.Ile273Val
NM_001369138.1:c.817A>G	NP_001356067.1:p.Ile273Val
NM_001369139.1:c.817A>G	NP_001356068.1:p.Ile273Val
NM_001369146.1:c.817A>G	NP_001356075.1:p.Ile273Val
NM_001369148.1:c.238A>G	NP_001356077.1:p.Ile80Val
NM_001369137.2:c.817A>G	NP_001356066.1:p.Ile273Val
NM_001369138.2:c.817A>G	NP_001356067.1:p.Ile273Val
NM_001369146.2:c.817A>G	NP_001356075.1:p.Ile273Val
NM_001369148.2:c.238A>G	NP_001356077.1:p.Ile80Val