Canonical Allele Identifier: CA398710582

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19575051G>T (hg19) ; chr17:g.19671738G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671738G>T , CM000679.2:g.19671738G>T	GRCh38
NC_000017.10:g.19575051G>T , CM000679.1:g.19575051G>T	GRCh37
NC_000017.9:g.19515643G>T	NCBI36
NG_007095.2:g.27988G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1225G>T MANE Select	ENSP00000176643.6:p.Ala409Ser
ENST00000395575.7:c.898G>T	ENSP00000378942.3:p.Ala300Ser
ENST00000472059.6:c.*783G>T	ENSP00000458397.1:n.*783G>T
ENST00000571163.2:c.227-3758G>T	ENSP00000459977.2:n.227-3758G>T
ENST00000573947.2:c.25G>T	ENSP00000462933.2:p.Ala9Ser
ENST00000574078.3:n.554G>T
ENST00000581518.6:c.1225G>T	ENSP00000461916.2:p.Ala409Ser
ENST00000582991.6:c.1125G>T	ENSP00000464153.1:p.Glu375Asp
ENST00000671878.1:c.1225G>T	ENSP00000500516.1:p.Ala409Ser
ENST00000672059.1:n.1576G>T
ENST00000672357.1:c.1225G>T	ENSP00000500092.1:p.Ala409Ser
ENST00000672465.1:c.1225G>T	ENSP00000500517.1:p.Ala409Ser
ENST00000672487.1:c.*405G>T	ENSP00000500740.1:n.*405G>T
ENST00000672564.1:n.2894G>T
ENST00000672567.1:c.1098+6691G>T
ENST00000672591.1:c.285G>T
ENST00000672608.1:n.2214G>T
ENST00000672709.1:c.1079G>T
ENST00000673064.1:n.1725G>T
ENST00000673136.1:c.1208-3758G>T	ENSP00000500380.1:n.1208-3758G>T
ENST00000673472.1:n.1561G>T
ENST00000673516.1:n.1685G>T
ENST00000176643.10:c.1225G>T	ENSP00000176643.6:p.Ala409Ser
ENST00000339618.8:c.1225G>T	ENSP00000345774.4:p.Ala409Ser
ENST00000395575.6:c.1225G>T	ENSP00000378942.2:p.Ala409Ser
ENST00000472059.5:c.*783G>T	ENSP00000458397.1:n.*783G>T
ENST00000476965.5:n.975G>T
ENST00000571163.1:c.227-3820G>T	ENSP00000459977.1:n.227-3820G>T
ENST00000573947.1:c.132G>T	ENSP00000462933.1:p.Glu44Asp
ENST00000579855.5:c.1225G>T	ENSP00000463637.1:p.Ala409Ser
ENST00000581518.5:c.1225G>T	ENSP00000461916.1:p.Ala409Ser
ENST00000582991.5:c.1125G>T	ENSP00000464153.1:p.Glu375Asp
ENST00000630662.2:c.227-3820G>T	ENSP00000487353.1:n.227-3820G>T
ENST00000631291.2:c.1125G>T	ENSP00000486085.1:p.Glu375Asp
NM_000382.2:c.1225G>T	NP_000373.1:p.Ala409Ser
NM_001031806.1:c.1225G>T	NP_001026976.1:p.Ala409Ser
XM_011523732.1:c.1225G>T	XP_011522034.1:p.Ala409Ser
XM_011523733.1:c.1225G>T	XP_011522035.1:p.Ala409Ser
XM_011523733.2:c.1225G>T	XP_011522035.1:p.Ala409Ser
XM_017024355.1:c.1208-3820G>T	XP_016879844.1:n.1208-3820G>T
XM_017024356.2:c.1225G>T	XP_016879845.1:p.Ala409Ser
XM_017024357.1:c.1225G>T	XP_016879846.1:p.Ala409Ser
XM_017024358.2:c.1208-3820G>T	XP_016879847.1:n.1208-3820G>T
XM_024450651.1:c.646G>T	XP_024306419.1:p.Ala216Ser
XM_024450652.1:c.646G>T	XP_024306420.1:p.Ala216Ser
NM_000382.3:c.1225G>T MANE Select	NP_000373.1:p.Ala409Ser
NM_001031806.2:c.1225G>T	NP_001026976.1:p.Ala409Ser
NM_001369136.1:c.1225G>T	NP_001356065.1:p.Ala409Ser
NM_001369137.1:c.1225G>T	NP_001356066.1:p.Ala409Ser
NM_001369138.1:c.1225G>T	NP_001356067.1:p.Ala409Ser
NM_001369139.1:c.1225G>T	NP_001356068.1:p.Ala409Ser
NM_001369146.1:c.1208-3820G>T	NP_001356075.1:n.1208-3820G>T
NM_001369148.1:c.646G>T	NP_001356077.1:p.Ala216Ser
NM_001369137.2:c.1225G>T	NP_001356066.1:p.Ala409Ser
NM_001369138.2:c.1225G>T	NP_001356067.1:p.Ala409Ser
NM_001369146.2:c.1208-3820G>T	NP_001356075.1:n.1208-3820G>T
NM_001369148.2:c.646G>T	NP_001356077.1:p.Ala216Ser