Canonical Allele Identifier: CA398710576

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19575049G>C (hg19) ; chr17:g.19671736G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671736G>C , CM000679.2:g.19671736G>C	GRCh38
NC_000017.10:g.19575049G>C , CM000679.1:g.19575049G>C	GRCh37
NC_000017.9:g.19515641G>C	NCBI36
NG_007095.2:g.27986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1223G>C MANE Select	ENSP00000176643.6:p.Gly408Ala
ENST00000395575.7:c.896G>C	ENSP00000378942.3:p.Gly299Ala
ENST00000472059.6:c.*781G>C	ENSP00000458397.1:n.*781G>C
ENST00000571163.2:c.227-3760G>C	ENSP00000459977.2:n.227-3760G>C
ENST00000573947.2:c.23G>C	ENSP00000462933.2:p.Gly8Ala
ENST00000574078.3:n.552G>C
ENST00000581518.6:c.1223G>C	ENSP00000461916.2:p.Gly408Ala
ENST00000582991.6:c.1123G>C	ENSP00000464153.1:p.Glu375Gln
ENST00000671878.1:c.1223G>C	ENSP00000500516.1:p.Gly408Ala
ENST00000672059.1:n.1574G>C
ENST00000672357.1:c.1223G>C	ENSP00000500092.1:p.Gly408Ala
ENST00000672465.1:c.1223G>C	ENSP00000500517.1:p.Gly408Ala
ENST00000672487.1:c.*403G>C	ENSP00000500740.1:n.*403G>C
ENST00000672564.1:n.2892G>C
ENST00000672567.1:c.1098+6689G>C
ENST00000672591.1:c.283G>C
ENST00000672608.1:n.2212G>C
ENST00000672709.1:c.1077G>C
ENST00000673064.1:n.1723G>C
ENST00000673136.1:c.1208-3760G>C	ENSP00000500380.1:n.1208-3760G>C
ENST00000673472.1:n.1559G>C
ENST00000673516.1:n.1683G>C
ENST00000176643.10:c.1223G>C	ENSP00000176643.6:p.Gly408Ala
ENST00000339618.8:c.1223G>C	ENSP00000345774.4:p.Gly408Ala
ENST00000395575.6:c.1223G>C	ENSP00000378942.2:p.Gly408Ala
ENST00000472059.5:c.*781G>C	ENSP00000458397.1:n.*781G>C
ENST00000476965.5:n.973G>C
ENST00000571163.1:c.227-3822G>C	ENSP00000459977.1:n.227-3822G>C
ENST00000573947.1:c.130G>C	ENSP00000462933.1:p.Glu44Gln
ENST00000579855.5:c.1223G>C	ENSP00000463637.1:p.Gly408Ala
ENST00000581518.5:c.1223G>C	ENSP00000461916.1:p.Gly408Ala
ENST00000582991.5:c.1123G>C	ENSP00000464153.1:p.Glu375Gln
ENST00000630662.2:c.227-3822G>C	ENSP00000487353.1:n.227-3822G>C
ENST00000631291.2:c.1123G>C	ENSP00000486085.1:p.Glu375Gln
NM_000382.2:c.1223G>C	NP_000373.1:p.Gly408Ala
NM_001031806.1:c.1223G>C	NP_001026976.1:p.Gly408Ala
XM_011523732.1:c.1223G>C	XP_011522034.1:p.Gly408Ala
XM_011523733.1:c.1223G>C	XP_011522035.1:p.Gly408Ala
XM_011523733.2:c.1223G>C	XP_011522035.1:p.Gly408Ala
XM_017024355.1:c.1208-3822G>C	XP_016879844.1:n.1208-3822G>C
XM_017024356.2:c.1223G>C	XP_016879845.1:p.Gly408Ala
XM_017024357.1:c.1223G>C	XP_016879846.1:p.Gly408Ala
XM_017024358.2:c.1208-3822G>C	XP_016879847.1:n.1208-3822G>C
XM_024450651.1:c.644G>C	XP_024306419.1:p.Gly215Ala
XM_024450652.1:c.644G>C	XP_024306420.1:p.Gly215Ala
NM_000382.3:c.1223G>C MANE Select	NP_000373.1:p.Gly408Ala
NM_001031806.2:c.1223G>C	NP_001026976.1:p.Gly408Ala
NM_001369136.1:c.1223G>C	NP_001356065.1:p.Gly408Ala
NM_001369137.1:c.1223G>C	NP_001356066.1:p.Gly408Ala
NM_001369138.1:c.1223G>C	NP_001356067.1:p.Gly408Ala
NM_001369139.1:c.1223G>C	NP_001356068.1:p.Gly408Ala
NM_001369146.1:c.1208-3822G>C	NP_001356075.1:n.1208-3822G>C
NM_001369148.1:c.644G>C	NP_001356077.1:p.Gly215Ala
NM_001369137.2:c.1223G>C	NP_001356066.1:p.Gly408Ala
NM_001369138.2:c.1223G>C	NP_001356067.1:p.Gly408Ala
NM_001369146.2:c.1208-3822G>C	NP_001356075.1:n.1208-3822G>C
NM_001369148.2:c.644G>C	NP_001356077.1:p.Gly215Ala