Canonical Allele Identifier: CA2741523182

Gene: ALDH3A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19655812T>C , CM000679.2:g.19655812T>C	GRCh38
NC_000017.10:g.19559125T>C , CM000679.1:g.19559125T>C	GRCh37
NC_000017.9:g.19499717T>C	NCBI36
NG_007095.2:g.12062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.472-554T>C MANE Select	ENSP00000176643.6:n.472-554T>C
ENST00000395575.7:c.471+3180T>C	ENSP00000378942.3:n.471+3180T>C
ENST00000472059.6:c.*29+425T>C	ENSP00000458397.1:n.*29+425T>C
ENST00000581518.6:c.472-554T>C	ENSP00000461916.2:n.472-554T>C
ENST00000582991.6:c.472-554T>C	ENSP00000464153.1:n.472-554T>C
ENST00000671841.1:n.427T>C
ENST00000671878.1:c.472-554T>C	ENSP00000500516.1:n.472-554T>C
ENST00000672059.1:n.922+425T>C
ENST00000672322.1:n.989T>C
ENST00000672357.1:c.472-554T>C	ENSP00000500092.1:n.472-554T>C
ENST00000672465.1:c.472-554T>C	ENSP00000500517.1:n.472-554T>C
ENST00000672487.1:c.472-554T>C	ENSP00000500740.1:n.472-554T>C
ENST00000672564.1:n.693-554T>C
ENST00000672567.1:c.363-554T>C
ENST00000672608.1:n.907T>C
ENST00000672709.1:c.326-554T>C
ENST00000673136.1:c.472-554T>C	ENSP00000500380.1:n.472-554T>C
ENST00000673472.1:n.807+425T>C
ENST00000176643.10:c.472-554T>C	ENSP00000176643.6:n.472-554T>C
ENST00000339618.8:c.472-554T>C	ENSP00000345774.4:n.472-554T>C
ENST00000395575.6:c.472-554T>C	ENSP00000378942.2:n.472-554T>C
ENST00000446398.6:c.472-554T>C	ENSP00000395845.2:n.472-554T>C
ENST00000472059.5:c.*29+425T>C	ENSP00000458397.1:n.*29+425T>C
ENST00000578614.1:c.*75-554T>C	ENSP00000463128.1:n.*75-554T>C
ENST00000579855.5:c.472-554T>C	ENSP00000463637.1:n.472-554T>C
ENST00000581518.5:c.472-554T>C	ENSP00000461916.1:n.472-554T>C
ENST00000582991.5:c.472-554T>C	ENSP00000464153.1:n.472-554T>C
ENST00000584332.6:c.376-554T>C	ENSP00000466814.1:n.376-554T>C
ENST00000630662.2:c.-510-554T>C	ENSP00000487353.1:n.-510-554T>C
ENST00000631291.2:c.472-554T>C	ENSP00000486085.1:n.472-554T>C
NM_000382.2:c.472-554T>C	NP_000373.1:n.472-554T>C
NM_001031806.1:c.472-554T>C	NP_001026976.1:n.472-554T>C
XM_011523732.1:c.472-554T>C	XP_011522034.1:n.472-554T>C
XM_011523733.1:c.472-554T>C	XP_011522035.1:n.472-554T>C
XM_011523733.2:c.472-554T>C	XP_011522035.1:n.472-554T>C
XM_017024355.1:c.472-554T>C	XP_016879844.1:n.472-554T>C
XM_017024356.2:c.472-554T>C	XP_016879845.1:n.472-554T>C
XM_017024357.1:c.472-554T>C	XP_016879846.1:n.472-554T>C
XM_017024358.2:c.472-554T>C	XP_016879847.1:n.472-554T>C
XM_024450651.1:c.-109+425T>C	XP_024306419.1:n.-109+425T>C
XM_024450652.1:c.-109+425T>C	XP_024306420.1:n.-109+425T>C
NM_000382.3:c.472-554T>C MANE Select	NP_000373.1:n.472-554T>C
NM_001031806.2:c.472-554T>C	NP_001026976.1:n.472-554T>C
NM_001369136.1:c.472-554T>C	NP_001356065.1:n.472-554T>C
NM_001369137.1:c.472-554T>C	NP_001356066.1:n.472-554T>C
NM_001369138.1:c.472-554T>C	NP_001356067.1:n.472-554T>C
NM_001369139.1:c.472-554T>C	NP_001356068.1:n.472-554T>C
NM_001369146.1:c.472-554T>C	NP_001356075.1:n.472-554T>C
NM_001369148.1:c.-109+425T>C	NP_001356077.1:n.-109+425T>C
NM_001369137.2:c.472-554T>C	NP_001356066.1:n.472-554T>C
NM_001369138.2:c.472-554T>C	NP_001356067.1:n.472-554T>C
NM_001369146.2:c.472-554T>C	NP_001356075.1:n.472-554T>C
NM_001369148.2:c.-109+425T>C	NP_001356077.1:n.-109+425T>C