Canonical Allele Identifier: CA398710982

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19575213A>G (hg19) ; chr17:g.19671900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671900A>G , CM000679.2:g.19671900A>G	GRCh38
NC_000017.10:g.19575213A>G , CM000679.1:g.19575213A>G	GRCh37
NC_000017.9:g.19515805A>G	NCBI36
NG_007095.2:g.28150A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1387A>G MANE Select	ENSP00000176643.6:p.Lys463Glu
ENST00000395575.7:c.1060A>G	ENSP00000378942.3:p.Lys354Glu
ENST00000472059.6:c.*945A>G	ENSP00000458397.1:n.*945A>G
ENST00000571163.2:c.227-3596A>G	ENSP00000459977.2:n.227-3596A>G
ENST00000573947.2:c.187A>G	ENSP00000462933.2:p.Lys63Glu
ENST00000574078.3:n.716A>G
ENST00000581518.6:c.1387A>G	ENSP00000461916.2:p.Lys463Glu
ENST00000582991.6:c.*105A>G	ENSP00000464153.1:n.*105A>G
ENST00000671878.1:c.1387A>G	ENSP00000500516.1:p.Lys463Glu
ENST00000672059.1:n.1738A>G
ENST00000672357.1:c.1387A>G	ENSP00000500092.1:p.Lys463Glu
ENST00000672465.1:c.1387A>G	ENSP00000500517.1:p.Lys463Glu
ENST00000672487.1:c.*567A>G	ENSP00000500740.1:n.*567A>G
ENST00000672564.1:n.3056A>G
ENST00000672567.1:c.1098+6853A>G
ENST00000672591.1:c.447A>G
ENST00000672608.1:n.2376A>G
ENST00000672709.1:c.1241A>G
ENST00000673064.1:n.1887A>G
ENST00000673136.1:c.1208-3596A>G	ENSP00000500380.1:n.1208-3596A>G
ENST00000673472.1:n.1723A>G
ENST00000673516.1:n.1847A>G
ENST00000176643.10:c.1387A>G	ENSP00000176643.6:p.Lys463Glu
ENST00000339618.8:c.1387A>G	ENSP00000345774.4:p.Lys463Glu
ENST00000395575.6:c.1387A>G	ENSP00000378942.2:p.Lys463Glu
ENST00000472059.5:c.*945A>G	ENSP00000458397.1:n.*945A>G
ENST00000476965.5:n.1137A>G
ENST00000571163.1:c.227-3658A>G	ENSP00000459977.1:n.227-3658A>G
ENST00000573565.1:c.102A>G
ENST00000573947.1:c.294A>G	ENSP00000462933.1:n.294A>G
ENST00000575384.2:c.133A>G	ENSP00000461235.2:p.Lys45Glu
ENST00000579855.5:c.1387A>G	ENSP00000463637.1:p.Lys463Glu
ENST00000581518.5:c.1387A>G	ENSP00000461916.1:p.Lys463Glu
ENST00000582991.5:c.*105A>G	ENSP00000464153.1:n.*105A>G
ENST00000630662.2:c.227-3658A>G	ENSP00000487353.1:n.227-3658A>G
ENST00000631291.2:c.*105A>G	ENSP00000486085.1:n.*105A>G
NM_000382.2:c.1387A>G	NP_000373.1:p.Lys463Glu
NM_001031806.1:c.1387A>G	NP_001026976.1:p.Lys463Glu
XM_011523732.1:c.1387A>G	XP_011522034.1:p.Lys463Glu
XM_011523733.1:c.1387A>G	XP_011522035.1:p.Lys463Glu
XM_011523733.2:c.1387A>G	XP_011522035.1:p.Lys463Glu
XM_017024355.1:c.1208-3658A>G	XP_016879844.1:n.1208-3658A>G
XM_017024356.2:c.1387A>G	XP_016879845.1:p.Lys463Glu
XM_017024357.1:c.1387A>G	XP_016879846.1:p.Lys463Glu
XM_017024358.2:c.1208-3658A>G	XP_016879847.1:n.1208-3658A>G
XM_024450651.1:c.808A>G	XP_024306419.1:p.Lys270Glu
XM_024450652.1:c.808A>G	XP_024306420.1:p.Lys270Glu
NM_000382.3:c.1387A>G MANE Select	NP_000373.1:p.Lys463Glu
NM_001031806.2:c.1387A>G	NP_001026976.1:p.Lys463Glu
NM_001369136.1:c.1387A>G	NP_001356065.1:p.Lys463Glu
NM_001369137.1:c.1387A>G	NP_001356066.1:p.Lys463Glu
NM_001369138.1:c.1387A>G	NP_001356067.1:p.Lys463Glu
NM_001369139.1:c.1387A>G	NP_001356068.1:p.Lys463Glu
NM_001369146.1:c.1208-3658A>G	NP_001356075.1:n.1208-3658A>G
NM_001369148.1:c.808A>G	NP_001356077.1:p.Lys270Glu
NM_001369137.2:c.1387A>G	NP_001356066.1:p.Lys463Glu
NM_001369138.2:c.1387A>G	NP_001356067.1:p.Lys463Glu
NM_001369146.2:c.1208-3658A>G	NP_001356075.1:n.1208-3658A>G
NM_001369148.2:c.808A>G	NP_001356077.1:p.Lys270Glu