Canonical Allele Identifier: CA3223273791
Community Standard Title: NM_000382.3(ALDH3A2):c.529C= (p.Arg177=)
Gene: ALDH3A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19656423C= , CM000679.2:g.19656423C= GRCh38
NC_000017.10:g.19559736C= , CM000679.1:g.19559736C= GRCh37
NC_000017.9:g.19500328C= NCBI36
NG_007095.2:g.12673C=

Transcript Alleles

HGVS Amino-acid Change
NM_000382.3:c.529C= MANE Select NP_000373.1:p.Arg177=
ENST00000176643.11:c.529C= MANE Select ENSP00000176643.6:p.Arg177=
NM_000382.2:c.529C= NP_000373.1:p.Arg177=
NM_001031806.1:c.529C= NP_001026976.1:p.Arg177=
NM_001031806.2:c.529C= NP_001026976.1:p.Arg177=
NM_001369136.1:c.529C= NP_001356065.1:p.Arg177=
NM_001369137.1:c.529C= NP_001356066.1:p.Arg177=
NM_001369137.2:c.529C= NP_001356066.1:p.Arg177=
NM_001369138.1:c.529C= NP_001356067.1:p.Arg177=
NM_001369138.2:c.529C= NP_001356067.1:p.Arg177=
NM_001369139.1:c.529C= NP_001356068.1:p.Arg177=
NM_001369146.1:c.529C= NP_001356075.1:p.Arg177=
NM_001369146.2:c.529C= NP_001356075.1:p.Arg177=
NM_001369148.1:c.-51C= NP_001356077.1:n.-51C=
NM_001369148.2:c.-51C= NP_001356077.1:n.-51C=
ENST00000176643.10:c.529C= ENSP00000176643.6:p.Arg177=
ENST00000339618.8:c.529C= ENSP00000345774.4:p.Arg177=
ENST00000395575.6:c.529C= ENSP00000378942.2:p.Arg177=
ENST00000395575.7:c.471+3791C= ENSP00000378942.3:n.471+3791C=
ENST00000472059.5:c.*87C= ENSP00000458397.1:n.*87C=
ENST00000472059.6:c.*87C= ENSP00000458397.1:n.*87C=
ENST00000476965.5:n.279C=
ENST00000571537.1:c.22C= ENSP00000458942.1:p.Arg8=
ENST00000578614.1:c.*132C= ENSP00000463128.1:n.*132C=
ENST00000579855.5:c.529C= ENSP00000463637.1:p.Arg177=
ENST00000581518.5:c.529C= ENSP00000461916.1:p.Arg177=
ENST00000581518.6:c.529C= ENSP00000461916.2:p.Arg177=
ENST00000582991.5:c.529C= ENSP00000464153.1:p.Arg177=
ENST00000582991.6:c.529C= ENSP00000464153.1:p.Arg177=
ENST00000630662.2:c.-453C= ENSP00000487353.1:n.-453C=
ENST00000631291.2:c.529C= ENSP00000486085.1:p.Arg177=
ENST00000671841.1:n.1038C=
ENST00000671878.1:c.529C= ENSP00000500516.1:p.Arg177=
ENST00000672059.1:n.980C=
ENST00000672322.1:n.1600C=
ENST00000672357.1:c.529C= ENSP00000500092.1:p.Arg177=
ENST00000672465.1:c.529C= ENSP00000500517.1:p.Arg177=
ENST00000672487.1:c.529C= ENSP00000500740.1:p.Arg177=
ENST00000672564.1:n.750C=
ENST00000672567.1:c.420C=
ENST00000672608.1:n.1518C=
ENST00000672709.1:c.383C=
ENST00000673136.1:c.529C= ENSP00000500380.1:p.Arg177=
ENST00000673472.1:n.865C=
XM_011523732.1:c.529C= XP_011522034.1:p.Arg177=
XM_011523733.1:c.529C= XP_011522035.1:p.Arg177=
XM_011523733.2:c.529C= XP_011522035.1:p.Arg177=
XM_017024355.1:c.529C= XP_016879844.1:p.Arg177=
XM_017024356.2:c.529C= XP_016879845.1:p.Arg177=
XM_017024357.1:c.529C= XP_016879846.1:p.Arg177=
XM_017024358.2:c.529C= XP_016879847.1:p.Arg177=
XM_024450651.1:c.-51C= XP_024306419.1:n.-51C=
XM_024450652.1:c.-51C= XP_024306420.1:n.-51C=