Canonical Allele Identifier: CA2838179936
Community Standard Title: NM_000382.3(ALDH3A2):c.943C= (p.Pro315=)
Gene: ALDH3A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19663335C= , CM000679.2:g.19663335C= GRCh38
NC_000017.10:g.19566648C= , CM000679.1:g.19566648C= GRCh37
NC_000017.9:g.19507240C= NCBI36
NG_007095.2:g.19585C=

Transcript Alleles

HGVS Amino-acid Change
NM_000382.3:c.943C= MANE Select NP_000373.1:p.Pro315=
ENST00000176643.11:c.943C= MANE Select ENSP00000176643.6:p.Pro315=
NM_000382.2:c.943C= NP_000373.1:p.Pro315=
NM_001031806.1:c.943C= NP_001026976.1:p.Pro315=
NM_001031806.2:c.943C= NP_001026976.1:p.Pro315=
NM_001369136.1:c.943C= NP_001356065.1:p.Pro315=
NM_001369137.1:c.943C= NP_001356066.1:p.Pro315=
NM_001369137.2:c.943C= NP_001356066.1:p.Pro315=
NM_001369138.1:c.943C= NP_001356067.1:p.Pro315=
NM_001369138.2:c.943C= NP_001356067.1:p.Pro315=
NM_001369139.1:c.943C= NP_001356068.1:p.Pro315=
NM_001369146.1:c.943C= NP_001356075.1:p.Pro315=
NM_001369146.2:c.943C= NP_001356075.1:p.Pro315=
NM_001369148.1:c.364C= NP_001356077.1:p.Pro122=
NM_001369148.2:c.364C= NP_001356077.1:p.Pro122=
ENST00000176643.10:c.943C= ENSP00000176643.6:p.Pro315=
ENST00000339618.8:c.943C= ENSP00000345774.4:p.Pro315=
ENST00000395575.6:c.943C= ENSP00000378942.2:p.Pro315=
ENST00000395575.7:c.616C= ENSP00000378942.3:p.Pro206=
ENST00000472059.5:c.*501C= ENSP00000458397.1:n.*501C=
ENST00000472059.6:c.*501C= ENSP00000458397.1:n.*501C=
ENST00000476965.5:n.693C=
ENST00000574078.2:n.272C=
ENST00000574078.3:n.272C=
ENST00000578696.1:c.374C=
ENST00000579855.5:c.943C= ENSP00000463637.1:p.Pro315=
ENST00000581518.5:c.943C= ENSP00000461916.1:p.Pro315=
ENST00000581518.6:c.943C= ENSP00000461916.2:p.Pro315=
ENST00000582991.5:c.943C= ENSP00000464153.1:p.Pro315=
ENST00000582991.6:c.943C= ENSP00000464153.1:p.Pro315=
ENST00000630662.2:c.-39C= ENSP00000487353.1:n.-39C=
ENST00000631291.2:c.943C= ENSP00000486085.1:p.Pro315=
ENST00000671878.1:c.943C= ENSP00000500516.1:p.Pro315=
ENST00000672059.1:n.1394C=
ENST00000672357.1:c.943C= ENSP00000500092.1:p.Pro315=
ENST00000672465.1:c.943C= ENSP00000500517.1:p.Pro315=
ENST00000672487.1:c.*123C= ENSP00000500740.1:n.*123C=
ENST00000672564.1:n.1164C=
ENST00000672567.1:c.834C=
ENST00000672591.1:c.3C=
ENST00000672608.1:n.1932C=
ENST00000672709.1:c.797C=
ENST00000673064.1:n.1443C=
ENST00000673136.1:c.943C= ENSP00000500380.1:p.Pro315=
ENST00000673472.1:n.1279C=
ENST00000673516.1:n.1403C=
XM_011523732.1:c.943C= XP_011522034.1:p.Pro315=
XM_011523733.1:c.943C= XP_011522035.1:p.Pro315=
XM_011523733.2:c.943C= XP_011522035.1:p.Pro315=
XM_017024355.1:c.943C= XP_016879844.1:p.Pro315=
XM_017024356.2:c.943C= XP_016879845.1:p.Pro315=
XM_017024357.1:c.943C= XP_016879846.1:p.Pro315=
XM_017024358.2:c.943C= XP_016879847.1:p.Pro315=
XM_024450651.1:c.364C= XP_024306419.1:p.Pro122=
XM_024450652.1:c.364C= XP_024306420.1:p.Pro122=