Canonical Allele Identifier: CA16607184
Gene: ALDH3A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 379490
dbSNP Id: rs1010078101

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19665042G>A , CM000679.2:g.19665042G>A GRCh38
NC_000017.10:g.19568355G>A , CM000679.1:g.19568355G>A GRCh37
NC_000017.9:g.19508947G>A NCBI36
NG_007095.2:g.21292G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000176643.11:c.1202G>A MANE Select ENSP00000176643.6:p.Gly401Glu
ENST00000395575.7:c.875G>A ENSP00000378942.3:p.Gly292Glu
ENST00000472059.6:c.*760G>A ENSP00000458397.1:n.*760G>A
ENST00000571163.2:c.221G>A ENSP00000459977.2:p.Gly74Glu
ENST00000573947.2:c.2G>A ENSP00000462933.2:p.Gly1Glu
ENST00000574078.3:n.531G>A
ENST00000581518.6:c.1202G>A ENSP00000461916.2:p.Gly401Glu
ENST00000582991.6:c.1107+1543G>A ENSP00000464153.1:n.1107+1543G>A
ENST00000671878.1:c.1202G>A ENSP00000500516.1:p.Gly401Glu
ENST00000672059.1:n.1558+1543G>A
ENST00000672357.1:c.1202G>A ENSP00000500092.1:p.Gly401Glu
ENST00000672465.1:c.1202G>A ENSP00000500517.1:p.Gly401Glu
ENST00000672487.1:c.*382G>A ENSP00000500740.1:n.*382G>A
ENST00000672564.1:n.2871G>A
ENST00000672567.1:c.1093G>A
ENST00000672591.1:c.262G>A
ENST00000672608.1:n.2191G>A
ENST00000672709.1:c.1056G>A
ENST00000673064.1:n.1702G>A
ENST00000673136.1:c.1202G>A ENSP00000500380.1:p.Gly401Glu
ENST00000673472.1:n.1538G>A
ENST00000673516.1:n.1662G>A
ENST00000176643.10:c.1202G>A ENSP00000176643.6:p.Gly401Glu
ENST00000339618.8:c.1202G>A ENSP00000345774.4:p.Gly401Glu
ENST00000395575.6:c.1202G>A ENSP00000378942.2:p.Gly401Glu
ENST00000472059.5:c.*760G>A ENSP00000458397.1:n.*760G>A
ENST00000476965.5:n.952G>A
ENST00000571163.1:c.221G>A ENSP00000459977.1:p.Gly74Glu
ENST00000573947.1:c.114+1543G>A ENSP00000462933.1:n.114+1543G>A
ENST00000579855.5:c.1202G>A ENSP00000463637.1:p.Gly401Glu
ENST00000581518.5:c.1202G>A ENSP00000461916.1:p.Gly401Glu
ENST00000582991.5:c.1107+1543G>A ENSP00000464153.1:n.1107+1543G>A
ENST00000630662.2:c.221G>A ENSP00000487353.1:p.Gly74Glu
ENST00000631291.2:c.1107+1543G>A ENSP00000486085.1:n.1107+1543G>A
NM_000382.2:c.1202G>A NP_000373.1:p.Gly401Glu
NM_001031806.1:c.1202G>A NP_001026976.1:p.Gly401Glu
XM_011523732.1:c.1202G>A XP_011522034.1:p.Gly401Glu
XM_011523733.1:c.1202G>A XP_011522035.1:p.Gly401Glu
XM_011523733.2:c.1202G>A XP_011522035.1:p.Gly401Glu
XM_017024355.1:c.1202G>A XP_016879844.1:p.Gly401Glu
XM_017024356.2:c.1202G>A XP_016879845.1:p.Gly401Glu
XM_017024357.1:c.1202G>A XP_016879846.1:p.Gly401Glu
XM_017024358.2:c.1202G>A XP_016879847.1:p.Gly401Glu
XM_024450651.1:c.623G>A XP_024306419.1:p.Gly208Glu
XM_024450652.1:c.623G>A XP_024306420.1:p.Gly208Glu
NM_000382.3:c.1202G>A MANE Select NP_000373.1:p.Gly401Glu
NM_001031806.2:c.1202G>A NP_001026976.1:p.Gly401Glu
NM_001369136.1:c.1202G>A NP_001356065.1:p.Gly401Glu
NM_001369137.1:c.1202G>A NP_001356066.1:p.Gly401Glu
NM_001369138.1:c.1202G>A NP_001356067.1:p.Gly401Glu
NM_001369139.1:c.1202G>A NP_001356068.1:p.Gly401Glu
NM_001369146.1:c.1202G>A NP_001356075.1:p.Gly401Glu
NM_001369148.1:c.623G>A NP_001356077.1:p.Gly208Glu
NM_001369137.2:c.1202G>A NP_001356066.1:p.Gly401Glu
NM_001369138.2:c.1202G>A NP_001356067.1:p.Gly401Glu
NM_001369146.2:c.1202G>A NP_001356075.1:p.Gly401Glu
NM_001369148.2:c.623G>A NP_001356077.1:p.Gly208Glu