Canonical Allele Identifier: CA115120
Gene: ALDH3A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1644
dbSNP Id: rs72547575

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19664997A>G , CM000679.2:g.19664997A>G GRCh38
NC_000017.10:g.19568310A>G , CM000679.1:g.19568310A>G GRCh37
NC_000017.9:g.19508902A>G NCBI36
NG_007095.2:g.21247A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000176643.11:c.1157A>G MANE Select ENSP00000176643.6:p.Asn386Ser
ENST00000395575.7:c.830A>G ENSP00000378942.3:p.Asn277Ser
ENST00000472059.6:c.*715A>G ENSP00000458397.1:n.*715A>G
ENST00000571163.2:c.176A>G ENSP00000459977.2:p.Asn59Ser
ENST00000574078.3:n.486A>G
ENST00000581518.6:c.1157A>G ENSP00000461916.2:p.Asn386Ser
ENST00000582991.6:c.1107+1498A>G ENSP00000464153.1:n.1107+1498A>G
ENST00000671878.1:c.1157A>G ENSP00000500516.1:p.Asn386Ser
ENST00000672059.1:n.1558+1498A>G
ENST00000672357.1:c.1157A>G ENSP00000500092.1:p.Asn386Ser
ENST00000672465.1:c.1157A>G ENSP00000500517.1:p.Asn386Ser
ENST00000672487.1:c.*337A>G ENSP00000500740.1:n.*337A>G
ENST00000672564.1:n.2826A>G
ENST00000672567.1:c.1048A>G
ENST00000672591.1:c.217A>G
ENST00000672608.1:n.2146A>G
ENST00000672709.1:c.1011A>G
ENST00000673064.1:n.1657A>G
ENST00000673136.1:c.1157A>G ENSP00000500380.1:p.Asn386Ser
ENST00000673472.1:n.1493A>G
ENST00000673516.1:n.1617A>G
ENST00000176643.10:c.1157A>G ENSP00000176643.6:p.Asn386Ser
ENST00000339618.8:c.1157A>G ENSP00000345774.4:p.Asn386Ser
ENST00000395575.6:c.1157A>G ENSP00000378942.2:p.Asn386Ser
ENST00000472059.5:c.*715A>G ENSP00000458397.1:n.*715A>G
ENST00000476965.5:n.907A>G
ENST00000571163.1:c.176A>G ENSP00000459977.1:p.Asn59Ser
ENST00000573947.1:c.114+1498A>G ENSP00000462933.1:n.114+1498A>G
ENST00000579855.5:c.1157A>G ENSP00000463637.1:p.Asn386Ser
ENST00000581518.5:c.1157A>G ENSP00000461916.1:p.Asn386Ser
ENST00000582991.5:c.1107+1498A>G ENSP00000464153.1:n.1107+1498A>G
ENST00000630662.2:c.176A>G ENSP00000487353.1:p.Asn59Ser
ENST00000631291.2:c.1107+1498A>G ENSP00000486085.1:n.1107+1498A>G
NM_000382.2:c.1157A>G NP_000373.1:p.Asn386Ser
NM_001031806.1:c.1157A>G NP_001026976.1:p.Asn386Ser
XM_011523732.1:c.1157A>G XP_011522034.1:p.Asn386Ser
XM_011523733.1:c.1157A>G XP_011522035.1:p.Asn386Ser
XM_011523733.2:c.1157A>G XP_011522035.1:p.Asn386Ser
XM_017024355.1:c.1157A>G XP_016879844.1:p.Asn386Ser
XM_017024356.2:c.1157A>G XP_016879845.1:p.Asn386Ser
XM_017024357.1:c.1157A>G XP_016879846.1:p.Asn386Ser
XM_017024358.2:c.1157A>G XP_016879847.1:p.Asn386Ser
XM_024450651.1:c.578A>G XP_024306419.1:p.Asn193Ser
XM_024450652.1:c.578A>G XP_024306420.1:p.Asn193Ser
NM_000382.3:c.1157A>G MANE Select NP_000373.1:p.Asn386Ser
NM_001031806.2:c.1157A>G NP_001026976.1:p.Asn386Ser
NM_001369136.1:c.1157A>G NP_001356065.1:p.Asn386Ser
NM_001369137.1:c.1157A>G NP_001356066.1:p.Asn386Ser
NM_001369138.1:c.1157A>G NP_001356067.1:p.Asn386Ser
NM_001369139.1:c.1157A>G NP_001356068.1:p.Asn386Ser
NM_001369146.1:c.1157A>G NP_001356075.1:p.Asn386Ser
NM_001369148.1:c.578A>G NP_001356077.1:p.Asn193Ser
NM_001369137.2:c.1157A>G NP_001356066.1:p.Asn386Ser
NM_001369138.2:c.1157A>G NP_001356067.1:p.Asn386Ser
NM_001369146.2:c.1157A>G NP_001356075.1:p.Asn386Ser
NM_001369148.2:c.578A>G NP_001356077.1:p.Asn193Ser