Canonical Allele Identifier: CA398710705

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19575095T>G (hg19) ; chr17:g.19671782T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671782T>G , CM000679.2:g.19671782T>G	GRCh38
NC_000017.10:g.19575095T>G , CM000679.1:g.19575095T>G	GRCh37
NC_000017.9:g.19515687T>G	NCBI36
NG_007095.2:g.28032T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1269T>G MANE Select	ENSP00000176643.6:p.Arg423=
ENST00000395575.7:c.942T>G	ENSP00000378942.3:p.Arg314=
ENST00000472059.6:c.*827T>G	ENSP00000458397.1:n.*827T>G
ENST00000571163.2:c.227-3714T>G	ENSP00000459977.2:n.227-3714T>G
ENST00000573947.2:c.69T>G	ENSP00000462933.2:p.Arg23=
ENST00000574078.3:n.598T>G
ENST00000581518.6:c.1269T>G	ENSP00000461916.2:p.Arg423=
ENST00000582991.6:c.1169T>G	ENSP00000464153.1:p.Val390Gly
ENST00000671878.1:c.1269T>G	ENSP00000500516.1:p.Arg423=
ENST00000672059.1:n.1620T>G
ENST00000672357.1:c.1269T>G	ENSP00000500092.1:p.Arg423=
ENST00000672465.1:c.1269T>G	ENSP00000500517.1:p.Arg423=
ENST00000672487.1:c.*449T>G	ENSP00000500740.1:n.*449T>G
ENST00000672564.1:n.2938T>G
ENST00000672567.1:c.1098+6735T>G
ENST00000672591.1:c.329T>G
ENST00000672608.1:n.2258T>G
ENST00000672709.1:c.1123T>G
ENST00000673064.1:n.1769T>G
ENST00000673136.1:c.1208-3714T>G	ENSP00000500380.1:n.1208-3714T>G
ENST00000673472.1:n.1605T>G
ENST00000673516.1:n.1729T>G
ENST00000176643.10:c.1269T>G	ENSP00000176643.6:p.Arg423=
ENST00000339618.8:c.1269T>G	ENSP00000345774.4:p.Arg423=
ENST00000395575.6:c.1269T>G	ENSP00000378942.2:p.Arg423=
ENST00000472059.5:c.*827T>G	ENSP00000458397.1:n.*827T>G
ENST00000476965.5:n.1019T>G
ENST00000571163.1:c.227-3776T>G	ENSP00000459977.1:n.227-3776T>G
ENST00000573947.1:c.176T>G	ENSP00000462933.1:p.Val59Gly
ENST00000575384.2:c.15T>G	ENSP00000461235.2:p.Arg5=
ENST00000579855.5:c.1269T>G	ENSP00000463637.1:p.Arg423=
ENST00000581518.5:c.1269T>G	ENSP00000461916.1:p.Arg423=
ENST00000582991.5:c.1169T>G	ENSP00000464153.1:p.Val390Gly
ENST00000630662.2:c.227-3776T>G	ENSP00000487353.1:n.227-3776T>G
ENST00000631291.2:c.1169T>G	ENSP00000486085.1:p.Val390Gly
NM_000382.2:c.1269T>G	NP_000373.1:p.Arg423=
NM_001031806.1:c.1269T>G	NP_001026976.1:p.Arg423=
XM_011523732.1:c.1269T>G	XP_011522034.1:p.Arg423=
XM_011523733.1:c.1269T>G	XP_011522035.1:p.Arg423=
XM_011523733.2:c.1269T>G	XP_011522035.1:p.Arg423=
XM_017024355.1:c.1208-3776T>G	XP_016879844.1:n.1208-3776T>G
XM_017024356.2:c.1269T>G	XP_016879845.1:p.Arg423=
XM_017024357.1:c.1269T>G	XP_016879846.1:p.Arg423=
XM_017024358.2:c.1208-3776T>G	XP_016879847.1:n.1208-3776T>G
XM_024450651.1:c.690T>G	XP_024306419.1:p.Arg230=
XM_024450652.1:c.690T>G	XP_024306420.1:p.Arg230=
NM_000382.3:c.1269T>G MANE Select	NP_000373.1:p.Arg423=
NM_001031806.2:c.1269T>G	NP_001026976.1:p.Arg423=
NM_001369136.1:c.1269T>G	NP_001356065.1:p.Arg423=
NM_001369137.1:c.1269T>G	NP_001356066.1:p.Arg423=
NM_001369138.1:c.1269T>G	NP_001356067.1:p.Arg423=
NM_001369139.1:c.1269T>G	NP_001356068.1:p.Arg423=
NM_001369146.1:c.1208-3776T>G	NP_001356075.1:n.1208-3776T>G
NM_001369148.1:c.690T>G	NP_001356077.1:p.Arg230=
NM_001369137.2:c.1269T>G	NP_001356066.1:p.Arg423=
NM_001369138.2:c.1269T>G	NP_001356067.1:p.Arg423=
NM_001369146.2:c.1208-3776T>G	NP_001356075.1:n.1208-3776T>G
NM_001369148.2:c.690T>G	NP_001356077.1:p.Arg230=