Canonical Allele Identifier: CA498608173

Gene: ALDH3A2

Linked Data

• ClinVar Variation Id: 2859498
• ClinVar RCV Id: RCV003701867
• gnomAD v4: 17-19649040-G-A
• MyVariant Identifiers: chr17:g.19552353G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19649040G>A , CM000679.2:g.19649040G>A	GRCh38
NC_000017.10:g.19552353G>A , CM000679.1:g.19552353G>A	GRCh37
NC_000017.9:g.19492945G>A	NCBI36
NG_007095.2:g.5290G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.69G>A MANE Select	ENSP00000176643.6:p.Arg23=
ENST00000395575.7:c.69G>A	ENSP00000378942.3:p.Arg23=
ENST00000446398.7:n.79G>A
ENST00000467473.6:n.192G>A
ENST00000472059.6:c.69G>A	ENSP00000458397.1:p.Arg23=
ENST00000581518.6:c.69G>A	ENSP00000461916.2:p.Arg23=
ENST00000582991.6:c.69G>A	ENSP00000464153.1:p.Arg23=
ENST00000671878.1:c.69G>A	ENSP00000500516.1:p.Arg23=
ENST00000672357.1:c.69G>A	ENSP00000500092.1:p.Arg23=
ENST00000672465.1:c.69G>A	ENSP00000500517.1:p.Arg23=
ENST00000672487.1:c.69G>A	ENSP00000500740.1:p.Arg23=
ENST00000672564.1:n.290G>A
ENST00000673136.1:c.69G>A	ENSP00000500380.1:p.Arg23=
ENST00000176643.10:c.69G>A	ENSP00000176643.6:p.Arg23=
ENST00000339618.8:c.69G>A	ENSP00000345774.4:p.Arg23=
ENST00000395575.6:c.69G>A	ENSP00000378942.2:p.Arg23=
ENST00000446398.6:c.69G>A	ENSP00000395845.2:p.Arg23=
ENST00000467473.5:n.226G>A
ENST00000472059.5:c.69G>A	ENSP00000458397.1:p.Arg23=
ENST00000578614.1:c.69G>A	ENSP00000463128.1:p.Arg23=
ENST00000579403.1:n.115G>A
ENST00000579855.5:c.69G>A	ENSP00000463637.1:p.Arg23=
ENST00000580550.5:c.69G>A	ENSP00000462964.1:p.Arg23=
ENST00000581518.5:c.69G>A	ENSP00000461916.1:p.Arg23=
ENST00000582991.5:c.69G>A	ENSP00000464153.1:p.Arg23=
ENST00000584332.6:c.-28G>A	ENSP00000466814.1:n.-28G>A
ENST00000626500.2:c.69G>A	ENSP00000486283.1:p.Arg23=
ENST00000630662.2:c.-913G>A	ENSP00000487353.1:n.-913G>A
ENST00000631291.2:c.69G>A	ENSP00000486085.1:p.Arg23=
NM_000382.2:c.69G>A	NP_000373.1:p.Arg23=
NM_001031806.1:c.69G>A	NP_001026976.1:p.Arg23=
XM_011523732.1:c.69G>A	XP_011522034.1:p.Arg23=
XM_011523733.1:c.69G>A	XP_011522035.1:p.Arg23=
XM_011523733.2:c.69G>A	XP_011522035.1:p.Arg23=
XM_017024355.1:c.69G>A	XP_016879844.1:p.Arg23=
XM_017024356.2:c.69G>A	XP_016879845.1:p.Arg23=
XM_017024357.1:c.69G>A	XP_016879846.1:p.Arg23=
XM_017024358.2:c.69G>A	XP_016879847.1:p.Arg23=
XM_024450652.1:c.-620G>A	XP_024306420.1:n.-620G>A
NM_000382.3:c.69G>A MANE Select	NP_000373.1:p.Arg23=
NM_001031806.2:c.69G>A	NP_001026976.1:p.Arg23=
NM_001369136.1:c.69G>A	NP_001356065.1:p.Arg23=
NM_001369137.1:c.69G>A	NP_001356066.1:p.Arg23=
NM_001369138.1:c.69G>A	NP_001356067.1:p.Arg23=
NM_001369139.1:c.69G>A	NP_001356068.1:p.Arg23=
NM_001369146.1:c.69G>A	NP_001356075.1:p.Arg23=
NM_001369148.1:c.-620G>A	NP_001356077.1:n.-620G>A
NM_001369137.2:c.69G>A	NP_001356066.1:p.Arg23=
NM_001369138.2:c.69G>A	NP_001356067.1:p.Arg23=
NM_001369146.2:c.69G>A	NP_001356075.1:p.Arg23=
NM_001369148.2:c.-620G>A	NP_001356077.1:n.-620G>A