Canonical Allele Identifier: CA398705818

Gene: ALDH3A2

Linked Data

• ClinVar Variation Id: 554479
• ClinVar RCV Id: RCV000670121
• MyVariant Identifiers: chr17:g.19559677A>G (hg19) ; chr17:g.19656364A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19656364A>G , CM000679.2:g.19656364A>G	GRCh38
NC_000017.10:g.19559677A>G , CM000679.1:g.19559677A>G	GRCh37
NC_000017.9:g.19500269A>G	NCBI36
NG_007095.2:g.12614A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.472-2A>G MANE Select	ENSP00000176643.6:n.472-2A>G
ENST00000395575.7:c.471+3732A>G	ENSP00000378942.3:n.471+3732A>G
ENST00000472059.6:c.*30-2A>G	ENSP00000458397.1:n.*30-2A>G
ENST00000581518.6:c.472-2A>G	ENSP00000461916.2:n.472-2A>G
ENST00000582991.6:c.472-2A>G	ENSP00000464153.1:n.472-2A>G
ENST00000671841.1:n.979A>G
ENST00000671878.1:c.472-2A>G	ENSP00000500516.1:n.472-2A>G
ENST00000672059.1:n.923-2A>G
ENST00000672322.1:n.1541A>G
ENST00000672357.1:c.472-2A>G	ENSP00000500092.1:n.472-2A>G
ENST00000672465.1:c.472-2A>G	ENSP00000500517.1:n.472-2A>G
ENST00000672487.1:c.472-2A>G	ENSP00000500740.1:n.472-2A>G
ENST00000672564.1:n.693-2A>G
ENST00000672567.1:c.363-2A>G
ENST00000672608.1:n.1459A>G
ENST00000672709.1:c.326-2A>G
ENST00000673136.1:c.472-2A>G	ENSP00000500380.1:n.472-2A>G
ENST00000673472.1:n.808-2A>G
ENST00000176643.10:c.472-2A>G	ENSP00000176643.6:n.472-2A>G
ENST00000339618.8:c.472-2A>G	ENSP00000345774.4:n.472-2A>G
ENST00000395575.6:c.472-2A>G	ENSP00000378942.2:n.472-2A>G
ENST00000446398.6:c.472-2A>G	ENSP00000395845.2:n.472-2A>G
ENST00000472059.5:c.*30-2A>G	ENSP00000458397.1:n.*30-2A>G
ENST00000476965.5:n.220A>G
ENST00000578614.1:c.*75-2A>G	ENSP00000463128.1:n.*75-2A>G
ENST00000579855.5:c.472-2A>G	ENSP00000463637.1:n.472-2A>G
ENST00000581518.5:c.472-2A>G	ENSP00000461916.1:n.472-2A>G
ENST00000582991.5:c.472-2A>G	ENSP00000464153.1:n.472-2A>G
ENST00000584332.6:c.376-2A>G	ENSP00000466814.1:n.376-2A>G
ENST00000630662.2:c.-510-2A>G	ENSP00000487353.1:n.-510-2A>G
ENST00000631291.2:c.472-2A>G	ENSP00000486085.1:n.472-2A>G
NM_000382.2:c.472-2A>G	NP_000373.1:n.472-2A>G
NM_001031806.1:c.472-2A>G	NP_001026976.1:n.472-2A>G
XM_011523732.1:c.472-2A>G	XP_011522034.1:n.472-2A>G
XM_011523733.1:c.472-2A>G	XP_011522035.1:n.472-2A>G
XM_011523733.2:c.472-2A>G	XP_011522035.1:n.472-2A>G
XM_017024355.1:c.472-2A>G	XP_016879844.1:n.472-2A>G
XM_017024356.2:c.472-2A>G	XP_016879845.1:n.472-2A>G
XM_017024357.1:c.472-2A>G	XP_016879846.1:n.472-2A>G
XM_017024358.2:c.472-2A>G	XP_016879847.1:n.472-2A>G
XM_024450651.1:c.-108-2A>G	XP_024306419.1:n.-108-2A>G
XM_024450652.1:c.-108-2A>G	XP_024306420.1:n.-108-2A>G
NM_000382.3:c.472-2A>G MANE Select	NP_000373.1:n.472-2A>G
NM_001031806.2:c.472-2A>G	NP_001026976.1:n.472-2A>G
NM_001369136.1:c.472-2A>G	NP_001356065.1:n.472-2A>G
NM_001369137.1:c.472-2A>G	NP_001356066.1:n.472-2A>G
NM_001369138.1:c.472-2A>G	NP_001356067.1:n.472-2A>G
NM_001369139.1:c.472-2A>G	NP_001356068.1:n.472-2A>G
NM_001369146.1:c.472-2A>G	NP_001356075.1:n.472-2A>G
NM_001369148.1:c.-108-2A>G	NP_001356077.1:n.-108-2A>G
NM_001369137.2:c.472-2A>G	NP_001356066.1:n.472-2A>G
NM_001369138.2:c.472-2A>G	NP_001356067.1:n.472-2A>G
NM_001369146.2:c.472-2A>G	NP_001356075.1:n.472-2A>G
NM_001369148.2:c.-108-2A>G	NP_001356077.1:n.-108-2A>G