Canonical Allele Identifier: CA2843146258

Gene: ALDH3A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19661076dup , CM000679.2:g.19661076dup	GRCh38
NC_000017.10:g.19564389dup , CM000679.1:g.19564389dup	GRCh37
NC_000017.9:g.19504981dup	NCBI36
NG_007095.2:g.17326dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.799-51dup MANE Select	ENSP00000176643.6:n.799-51dup
ENST00000395575.7:c.472-51dup	ENSP00000378942.3:n.472-51dup
ENST00000472059.6:c.*357-51dup	ENSP00000458397.1:n.*357-51dup
ENST00000574078.3:n.128-51dup
ENST00000581518.6:c.799-51dup	ENSP00000461916.2:n.799-51dup
ENST00000582991.6:c.799-51dup	ENSP00000464153.1:n.799-51dup
ENST00000671841.1:n.2478-51dup
ENST00000671878.1:c.799-51dup	ENSP00000500516.1:n.799-51dup
ENST00000672059.1:n.1250-51dup
ENST00000672357.1:c.799-51dup	ENSP00000500092.1:n.799-51dup
ENST00000672465.1:c.799-51dup	ENSP00000500517.1:n.799-51dup
ENST00000672487.1:c.681-51dup	ENSP00000500740.1:n.681-51dup
ENST00000672564.1:n.1020-51dup
ENST00000672567.1:c.690-51dup
ENST00000672608.1:n.1788-51dup
ENST00000672709.1:c.653-51dup
ENST00000673064.1:n.1248dup
ENST00000673136.1:c.799-51dup	ENSP00000500380.1:n.799-51dup
ENST00000673472.1:n.1135-51dup
ENST00000673516.1:n.1208dup
ENST00000176643.10:c.799-51dup	ENSP00000176643.6:n.799-51dup
ENST00000339618.8:c.799-51dup	ENSP00000345774.4:n.799-51dup
ENST00000395575.6:c.799-51dup	ENSP00000378942.2:n.799-51dup
ENST00000472059.5:c.*357-51dup	ENSP00000458397.1:n.*357-51dup
ENST00000476965.5:n.549-51dup
ENST00000571537.1:c.292-51dup	ENSP00000458942.1:n.292-51dup
ENST00000574078.2:n.128-51dup
ENST00000578696.1:c.230-51dup
ENST00000579855.5:c.799-51dup	ENSP00000463637.1:n.799-51dup
ENST00000581518.5:c.799-51dup	ENSP00000461916.1:n.799-51dup
ENST00000582991.5:c.799-51dup	ENSP00000464153.1:n.799-51dup
ENST00000630662.2:c.-183-51dup	ENSP00000487353.1:n.-183-51dup
ENST00000631291.2:c.799-51dup	ENSP00000486085.1:n.799-51dup
NM_000382.2:c.799-51dup	NP_000373.1:n.799-51dup
NM_001031806.1:c.799-51dup	NP_001026976.1:n.799-51dup
XM_011523732.1:c.799-51dup	XP_011522034.1:n.799-51dup
XM_011523733.1:c.799-51dup	XP_011522035.1:n.799-51dup
XM_011523733.2:c.799-51dup	XP_011522035.1:n.799-51dup
XM_017024355.1:c.799-51dup	XP_016879844.1:n.799-51dup
XM_017024356.2:c.799-51dup	XP_016879845.1:n.799-51dup
XM_017024357.1:c.799-51dup	XP_016879846.1:n.799-51dup
XM_017024358.2:c.799-51dup	XP_016879847.1:n.799-51dup
XM_024450651.1:c.220-51dup	XP_024306419.1:n.220-51dup
XM_024450652.1:c.220-51dup	XP_024306420.1:n.220-51dup
NM_000382.3:c.799-51dup MANE Select	NP_000373.1:n.799-51dup
NM_001031806.2:c.799-51dup	NP_001026976.1:n.799-51dup
NM_001369136.1:c.799-51dup	NP_001356065.1:n.799-51dup
NM_001369137.1:c.799-51dup	NP_001356066.1:n.799-51dup
NM_001369138.1:c.799-51dup	NP_001356067.1:n.799-51dup
NM_001369139.1:c.799-51dup	NP_001356068.1:n.799-51dup
NM_001369146.1:c.799-51dup	NP_001356075.1:n.799-51dup
NM_001369148.1:c.220-51dup	NP_001356077.1:n.220-51dup
NM_001369137.2:c.799-51dup	NP_001356066.1:n.799-51dup
NM_001369138.2:c.799-51dup	NP_001356067.1:n.799-51dup
NM_001369146.2:c.799-51dup	NP_001356075.1:n.799-51dup
NM_001369148.2:c.220-51dup	NP_001356077.1:n.220-51dup