Canonical Allele Identifier: CA2580092705
Gene: ALDH3A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416519
ClinVar RCV Id: RCV003107268

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19671816_19671827delinsAGTTGGG , CM000679.2:g.19671816_19671827delinsAGTTGGG GRCh38
NC_000017.10:g.19575129_19575140delinsAGTTGGG , CM000679.1:g.19575129_19575140delinsAGTTGGG GRCh37
NC_000017.9:g.19515721_19515732delinsAGTTGGG NCBI36
NG_007095.2:g.28066_28077delinsAGTTGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000176643.11:c.1303_1314delinsAGTTGGG MANE Select ENSP00000176643.6:p.Ala435SerfsTer?
ENST00000395575.7:c.976_987delinsAGTTGGG ENSP00000378942.3:p.Ala326SerfsTer?
ENST00000472059.6:c.*861_*872delinsAGTTGGG ENSP00000458397.1:n.*861_*872delinsAGTTGG...
ENST00000571163.2:c.227-3680_227-3669delinsAGTTGGG ENSP00000459977.2:n.227-3680_227-3669deli...
ENST00000573947.2:c.103_114delinsAGTTGGG ENSP00000462933.2:p.Ala35SerfsTer?
ENST00000574078.3:n.632_643delinsAGTTGGG
ENST00000581518.6:c.1303_1314delinsAGTTGGG ENSP00000461916.2:p.Ala435SerfsTer?
ENST00000582991.6:c.*21_*32delinsAGTTGGG ENSP00000464153.1:n.*21_*32delinsAGTTGGG
ENST00000671878.1:c.1303_1314delinsAGTTGGG ENSP00000500516.1:p.Ala435SerfsTer?
ENST00000672059.1:n.1654_1665delinsAGTTGGG
ENST00000672357.1:c.1303_1314delinsAGTTGGG ENSP00000500092.1:p.Ala435SerfsTer?
ENST00000672465.1:c.1303_1314delinsAGTTGGG ENSP00000500517.1:p.Ala435SerfsTer?
ENST00000672487.1:c.*483_*494delinsAGTTGGG ENSP00000500740.1:n.*483_*494delinsAGTTGG...
ENST00000672564.1:n.2972_2983delinsAGTTGGG
ENST00000672567.1:c.1098+6769_1098+6780delinsAGTTGGG
ENST00000672591.1:c.363_374delinsAGTTGGG
ENST00000672608.1:n.2292_2303delinsAGTTGGG
ENST00000672709.1:c.1157_1168delinsAGTTGGG
ENST00000673064.1:n.1803_1814delinsAGTTGGG
ENST00000673136.1:c.1208-3680_1208-3669delinsAGTTGGG ENSP00000500380.1:n.1208-3680_1208-3669de...
ENST00000673472.1:n.1639_1650delinsAGTTGGG
ENST00000673516.1:n.1763_1774delinsAGTTGGG
ENST00000176643.10:c.1303_1314delinsAGTTGGG ENSP00000176643.6:p.Ala435SerfsTer?
ENST00000339618.8:c.1303_1314delinsAGTTGGG ENSP00000345774.4:p.Ala435SerfsTer?
ENST00000395575.6:c.1303_1314delinsAGTTGGG ENSP00000378942.2:p.Ala435SerfsTer?
ENST00000472059.5:c.*861_*872delinsAGTTGGG ENSP00000458397.1:n.*861_*872delinsAGTTGG...
ENST00000476965.5:n.1053_1064delinsAGTTGGG
ENST00000571163.1:c.227-3742_227-3731delinsAGTTGGG ENSP00000459977.1:n.227-3742_227-3731deli...
ENST00000573565.1:c.18_29delinsAGTTGGG
ENST00000573947.1:c.210_221delinsAGTTGGG ENSP00000462933.1:n.210_221delinsAGTTGGG
ENST00000575384.2:c.49_60delinsAGTTGGG ENSP00000461235.2:p.Ala17SerfsTer?
ENST00000579855.5:c.1303_1314delinsAGTTGGG ENSP00000463637.1:p.Ala435SerfsTer?
ENST00000581518.5:c.1303_1314delinsAGTTGGG ENSP00000461916.1:p.Ala435SerfsTer?
ENST00000582991.5:c.*21_*32delinsAGTTGGG ENSP00000464153.1:n.*21_*32delinsAGTTGGG
ENST00000630662.2:c.227-3742_227-3731delinsAGTTGGG ENSP00000487353.1:n.227-3742_227-3731deli...
ENST00000631291.2:c.*21_*32delinsAGTTGGG ENSP00000486085.1:n.*21_*32delinsAGTTGGG
NM_000382.2:c.1303_1314delinsAGTTGGG NP_000373.1:p.Ala435SerfsTer?
NM_001031806.1:c.1303_1314delinsAGTTGGG NP_001026976.1:p.Ala435SerfsTer?
XM_011523732.1:c.1303_1314delinsAGTTGGG XP_011522034.1:p.Ala435SerfsTer?
XM_011523733.1:c.1303_1314delinsAGTTGGG XP_011522035.1:p.Ala435SerfsTer?
XM_011523733.2:c.1303_1314delinsAGTTGGG XP_011522035.1:p.Ala435SerfsTer?
XM_017024355.1:c.1208-3742_1208-3731delinsAGTTGGG XP_016879844.1:n.1208-3742_1208-3731delin...
XM_017024356.2:c.1303_1314delinsAGTTGGG XP_016879845.1:p.Ala435SerfsTer?
XM_017024357.1:c.1303_1314delinsAGTTGGG XP_016879846.1:p.Ala435SerfsTer?
XM_017024358.2:c.1208-3742_1208-3731delinsAGTTGGG XP_016879847.1:n.1208-3742_1208-3731delin...
XM_024450651.1:c.724_735delinsAGTTGGG XP_024306419.1:p.Ala242SerfsTer?
XM_024450652.1:c.724_735delinsAGTTGGG XP_024306420.1:p.Ala242SerfsTer?
NM_000382.3:c.1303_1314delinsAGTTGGG MANE Select NP_000373.1:p.Ala435SerfsTer?
NM_001031806.2:c.1303_1314delinsAGTTGGG NP_001026976.1:p.Ala435SerfsTer?
NM_001369136.1:c.1303_1314delinsAGTTGGG NP_001356065.1:p.Ala435SerfsTer?
NM_001369137.1:c.1303_1314delinsAGTTGGG NP_001356066.1:p.Ala435SerfsTer?
NM_001369138.1:c.1303_1314delinsAGTTGGG NP_001356067.1:p.Ala435SerfsTer?
NM_001369139.1:c.1303_1314delinsAGTTGGG NP_001356068.1:p.Ala435SerfsTer?
NM_001369146.1:c.1208-3742_1208-3731delinsAGTTGGG NP_001356075.1:n.1208-3742_1208-3731delin...
NM_001369148.1:c.724_735delinsAGTTGGG NP_001356077.1:p.Ala242SerfsTer?
NM_001369137.2:c.1303_1314delinsAGTTGGG NP_001356066.1:p.Ala435SerfsTer?
NM_001369138.2:c.1303_1314delinsAGTTGGG NP_001356067.1:p.Ala435SerfsTer?
NM_001369146.2:c.1208-3742_1208-3731delinsAGTTGGG NP_001356075.1:n.1208-3742_1208-3731delin...
NM_001369148.2:c.724_735delinsAGTTGGG NP_001356077.1:p.Ala242SerfsTer?