Canonical Allele Identifier: CA288537209
Gene: ALDH3A2 HGNC NCBI

Linked Data

dbSNP Id: rs375453263

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19648844dup , CM000679.2:g.19648844dup GRCh38
NC_000017.10:g.19552157dup , CM000679.1:g.19552157dup GRCh37
NC_000017.9:g.19492749dup NCBI36
NG_007095.2:g.5094dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000176643.11:c.-128dup MANE Select ENSP00000176643.6:n.-128dup
ENST00000395575.7:c.-128dup ENSP00000378942.3:n.-128dup
ENST00000467473.6:n.87-91dup
ENST00000581518.6:c.-37-91dup ENSP00000461916.2:n.-37-91dup
ENST00000582991.6:c.-38+1dup ENSP00000464153.1:n.-38+1dup
ENST00000671878.1:c.-128dup ENSP00000500516.1:n.-128dup
ENST00000672357.1:c.-38+1dup ENSP00000500092.1:n.-38+1dup
ENST00000672465.1:c.-37-91dup ENSP00000500517.1:n.-37-91dup
ENST00000672487.1:c.-128dup ENSP00000500740.1:n.-128dup
ENST00000672564.1:n.94dup
ENST00000673136.1:c.-37-91dup ENSP00000500380.1:n.-37-91dup
ENST00000176643.10:c.-128dup ENSP00000176643.6:n.-128dup
ENST00000339618.8:c.-128dup ENSP00000345774.4:n.-128dup
ENST00000395575.6:c.-38+1dup ENSP00000378942.2:n.-38+1dup
ENST00000446398.6:c.-37-91dup ENSP00000395845.2:n.-37-91dup
ENST00000467473.5:n.121-91dup
ENST00000578614.1:c.-128dup ENSP00000463128.1:n.-128dup
ENST00000579855.5:c.-20+14dup ENSP00000463637.1:n.-20+14dup
ENST00000580550.5:c.-9-119dup ENSP00000462964.1:n.-9-119dup
ENST00000581518.5:c.-128dup ENSP00000461916.1:n.-128dup
ENST00000582991.5:c.-128dup ENSP00000464153.1:n.-128dup
ENST00000584332.6:c.-100dup ENSP00000466814.1:n.-100dup
ENST00000626500.2:c.-128dup ENSP00000486283.1:n.-128dup
ENST00000630662.2:c.-1109dup ENSP00000487353.1:n.-1109dup
ENST00000631291.2:c.-128dup ENSP00000486085.1:n.-128dup
NM_000382.2:c.-128dup NP_000373.1:n.-128dup
NM_001031806.1:c.-128dup NP_001026976.1:n.-128dup
XM_011523732.1:c.-38+1dup XP_011522034.1:n.-38+1dup
XM_011523733.1:c.-37-91dup XP_011522035.1:n.-37-91dup
XM_011523733.2:c.-37-91dup XP_011522035.1:n.-37-91dup
XM_017024356.2:c.-37-91dup XP_016879845.1:n.-37-91dup
XM_017024357.1:c.-38+1dup XP_016879846.1:n.-38+1dup
XM_017024358.2:c.-37-91dup XP_016879847.1:n.-37-91dup
XM_024450652.1:c.-725-91dup XP_024306420.1:n.-725-91dup
NM_000382.3:c.-128dup MANE Select NP_000373.1:n.-128dup
NM_001031806.2:c.-128dup NP_001026976.1:n.-128dup
NM_001369136.1:c.-38+1dup NP_001356065.1:n.-38+1dup
NM_001369137.1:c.-37-91dup NP_001356066.1:n.-37-91dup
NM_001369138.1:c.-37-91dup NP_001356067.1:n.-37-91dup
NM_001369139.1:c.-38+1dup NP_001356068.1:n.-38+1dup
NM_001369146.1:c.-37-91dup NP_001356075.1:n.-37-91dup
NM_001369148.1:c.-725-91dup NP_001356077.1:n.-725-91dup
NM_001369137.2:c.-37-91dup NP_001356066.1:n.-37-91dup
NM_001369138.2:c.-37-91dup NP_001356067.1:n.-37-91dup
NM_001369146.2:c.-37-91dup NP_001356075.1:n.-37-91dup
NM_001369148.2:c.-725-91dup NP_001356077.1:n.-725-91dup