Canonical Allele Identifier: CA398709300

Gene: ALDH3A2

Linked Data

• gnomAD v4: 17-19661218-G-A
• MyVariant Identifiers: chr17:g.19564531G>A (hg19) ; chr17:g.19661218G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19661218G>A , CM000679.2:g.19661218G>A	GRCh38
NC_000017.10:g.19564531G>A , CM000679.1:g.19564531G>A	GRCh37
NC_000017.9:g.19505123G>A	NCBI36
NG_007095.2:g.17468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.890G>A MANE Select	ENSP00000176643.6:p.Gly297Glu
ENST00000395575.7:c.563G>A	ENSP00000378942.3:p.Gly188Glu
ENST00000472059.6:c.*448G>A	ENSP00000458397.1:n.*448G>A
ENST00000574078.3:n.219G>A
ENST00000581518.6:c.890G>A	ENSP00000461916.2:p.Gly297Glu
ENST00000582991.6:c.890G>A	ENSP00000464153.1:p.Gly297Glu
ENST00000671841.1:n.2569G>A
ENST00000671878.1:c.890G>A	ENSP00000500516.1:p.Gly297Glu
ENST00000672059.1:n.1341G>A
ENST00000672357.1:c.890G>A	ENSP00000500092.1:p.Gly297Glu
ENST00000672465.1:c.890G>A	ENSP00000500517.1:p.Gly297Glu
ENST00000672487.1:c.*70G>A	ENSP00000500740.1:n.*70G>A
ENST00000672564.1:n.1111G>A
ENST00000672567.1:c.781G>A
ENST00000672608.1:n.1879G>A
ENST00000672709.1:c.744G>A
ENST00000673064.1:n.1390G>A
ENST00000673136.1:c.890G>A	ENSP00000500380.1:p.Gly297Glu
ENST00000673472.1:n.1226G>A
ENST00000673516.1:n.1350G>A
ENST00000176643.10:c.890G>A	ENSP00000176643.6:p.Gly297Glu
ENST00000339618.8:c.890G>A	ENSP00000345774.4:p.Gly297Glu
ENST00000395575.6:c.890G>A	ENSP00000378942.2:p.Gly297Glu
ENST00000472059.5:c.*448G>A	ENSP00000458397.1:n.*448G>A
ENST00000476965.5:n.640G>A
ENST00000571537.1:c.383G>A	ENSP00000458942.1:p.Gly128Glu
ENST00000574078.2:n.219G>A
ENST00000578696.1:c.321G>A
ENST00000579855.5:c.890G>A	ENSP00000463637.1:p.Gly297Glu
ENST00000581518.5:c.890G>A	ENSP00000461916.1:p.Gly297Glu
ENST00000582991.5:c.890G>A	ENSP00000464153.1:p.Gly297Glu
ENST00000630662.2:c.-92G>A	ENSP00000487353.1:n.-92G>A
ENST00000631291.2:c.890G>A	ENSP00000486085.1:p.Gly297Glu
NM_000382.2:c.890G>A	NP_000373.1:p.Gly297Glu
NM_001031806.1:c.890G>A	NP_001026976.1:p.Gly297Glu
XM_011523732.1:c.890G>A	XP_011522034.1:p.Gly297Glu
XM_011523733.1:c.890G>A	XP_011522035.1:p.Gly297Glu
XM_011523733.2:c.890G>A	XP_011522035.1:p.Gly297Glu
XM_017024355.1:c.890G>A	XP_016879844.1:p.Gly297Glu
XM_017024356.2:c.890G>A	XP_016879845.1:p.Gly297Glu
XM_017024357.1:c.890G>A	XP_016879846.1:p.Gly297Glu
XM_017024358.2:c.890G>A	XP_016879847.1:p.Gly297Glu
XM_024450651.1:c.311G>A	XP_024306419.1:p.Gly104Glu
XM_024450652.1:c.311G>A	XP_024306420.1:p.Gly104Glu
NM_000382.3:c.890G>A MANE Select	NP_000373.1:p.Gly297Glu
NM_001031806.2:c.890G>A	NP_001026976.1:p.Gly297Glu
NM_001369136.1:c.890G>A	NP_001356065.1:p.Gly297Glu
NM_001369137.1:c.890G>A	NP_001356066.1:p.Gly297Glu
NM_001369138.1:c.890G>A	NP_001356067.1:p.Gly297Glu
NM_001369139.1:c.890G>A	NP_001356068.1:p.Gly297Glu
NM_001369146.1:c.890G>A	NP_001356075.1:p.Gly297Glu
NM_001369148.1:c.311G>A	NP_001356077.1:p.Gly104Glu
NM_001369137.2:c.890G>A	NP_001356066.1:p.Gly297Glu
NM_001369138.2:c.890G>A	NP_001356067.1:p.Gly297Glu
NM_001369146.2:c.890G>A	NP_001356075.1:p.Gly297Glu
NM_001369148.2:c.311G>A	NP_001356077.1:p.Gly104Glu