Canonical Allele Identifier: CA2636599126
Gene: ALDH3A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19671700dup , CM000679.2:g.19671700dup GRCh38
NC_000017.10:g.19575013dup , CM000679.1:g.19575013dup GRCh37
NC_000017.9:g.19515605dup NCBI36
NG_007095.2:g.27950dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000176643.11:c.1208-21dup MANE Select ENSP00000176643.6:n.1208-21dup
ENST00000395575.7:c.881-21dup ENSP00000378942.3:n.881-21dup
ENST00000472059.6:c.*766-21dup ENSP00000458397.1:n.*766-21dup
ENST00000571163.2:c.227-3796dup ENSP00000459977.2:n.227-3796dup
ENST00000573947.2:c.8-21dup ENSP00000462933.2:n.8-21dup
ENST00000574078.3:n.537-21dup
ENST00000581518.6:c.1208-21dup ENSP00000461916.2:n.1208-21dup
ENST00000582991.6:c.1108-21dup ENSP00000464153.1:n.1108-21dup
ENST00000671878.1:c.1208-21dup ENSP00000500516.1:n.1208-21dup
ENST00000672059.1:n.1559-21dup
ENST00000672357.1:c.1208-21dup ENSP00000500092.1:n.1208-21dup
ENST00000672465.1:c.1208-21dup ENSP00000500517.1:n.1208-21dup
ENST00000672487.1:c.*388-21dup ENSP00000500740.1:n.*388-21dup
ENST00000672564.1:n.2877-21dup
ENST00000672567.1:c.1098+6653dup
ENST00000672591.1:c.268-21dup
ENST00000672608.1:n.2197-21dup
ENST00000672709.1:c.1062-21dup
ENST00000673064.1:n.1708-21dup
ENST00000673136.1:c.1208-3796dup ENSP00000500380.1:n.1208-3796dup
ENST00000673472.1:n.1544-21dup
ENST00000673516.1:n.1668-21dup
ENST00000176643.10:c.1208-21dup ENSP00000176643.6:n.1208-21dup
ENST00000339618.8:c.1208-21dup ENSP00000345774.4:n.1208-21dup
ENST00000395575.6:c.1208-21dup ENSP00000378942.2:n.1208-21dup
ENST00000472059.5:c.*766-21dup ENSP00000458397.1:n.*766-21dup
ENST00000476965.5:n.958-21dup
ENST00000571163.1:c.227-3858dup ENSP00000459977.1:n.227-3858dup
ENST00000573947.1:c.115-21dup ENSP00000462933.1:n.115-21dup
ENST00000579855.5:c.1208-21dup ENSP00000463637.1:n.1208-21dup
ENST00000581518.5:c.1208-21dup ENSP00000461916.1:n.1208-21dup
ENST00000582991.5:c.1108-21dup ENSP00000464153.1:n.1108-21dup
ENST00000630662.2:c.227-3858dup ENSP00000487353.1:n.227-3858dup
ENST00000631291.2:c.1108-21dup ENSP00000486085.1:n.1108-21dup
NM_000382.2:c.1208-21dup NP_000373.1:n.1208-21dup
NM_001031806.1:c.1208-21dup NP_001026976.1:n.1208-21dup
XM_011523732.1:c.1208-21dup XP_011522034.1:n.1208-21dup
XM_011523733.1:c.1208-21dup XP_011522035.1:n.1208-21dup
XM_011523733.2:c.1208-21dup XP_011522035.1:n.1208-21dup
XM_017024355.1:c.1208-3858dup XP_016879844.1:n.1208-3858dup
XM_017024356.2:c.1208-21dup XP_016879845.1:n.1208-21dup
XM_017024357.1:c.1208-21dup XP_016879846.1:n.1208-21dup
XM_017024358.2:c.1208-3858dup XP_016879847.1:n.1208-3858dup
XM_024450651.1:c.629-21dup XP_024306419.1:n.629-21dup
XM_024450652.1:c.629-21dup XP_024306420.1:n.629-21dup
NM_000382.3:c.1208-21dup MANE Select NP_000373.1:n.1208-21dup
NM_001031806.2:c.1208-21dup NP_001026976.1:n.1208-21dup
NM_001369136.1:c.1208-21dup NP_001356065.1:n.1208-21dup
NM_001369137.1:c.1208-21dup NP_001356066.1:n.1208-21dup
NM_001369138.1:c.1208-21dup NP_001356067.1:n.1208-21dup
NM_001369139.1:c.1208-21dup NP_001356068.1:n.1208-21dup
NM_001369146.1:c.1208-3858dup NP_001356075.1:n.1208-3858dup
NM_001369148.1:c.629-21dup NP_001356077.1:n.629-21dup
NM_001369137.2:c.1208-21dup NP_001356066.1:n.1208-21dup
NM_001369138.2:c.1208-21dup NP_001356067.1:n.1208-21dup
NM_001369146.2:c.1208-3858dup NP_001356075.1:n.1208-3858dup
NM_001369148.2:c.629-21dup NP_001356077.1:n.629-21dup