Canonical Allele Identifier: CA2695224567

Gene: ALDH3A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19657867_19657868del , CM000679.2:g.19657867_19657868del	GRCh38
NC_000017.10:g.19561180_19561181del , CM000679.1:g.19561180_19561181del	GRCh37
NC_000017.9:g.19501772_19501773del	NCBI36
NG_007095.2:g.14117_14118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.798+5_798+6del MANE Select	ENSP00000176643.6:n.798+5_798+6del
ENST00000395575.7:c.472-3260_472-3259del	ENSP00000378942.3:n.472-3260_472-3259del
ENST00000472059.6:c.*356+5_*356+6del	ENSP00000458397.1:n.*356+5_*356+6del
ENST00000581518.6:c.798+5_798+6del	ENSP00000461916.2:n.798+5_798+6del
ENST00000582991.6:c.798+5_798+6del	ENSP00000464153.1:n.798+5_798+6del
ENST00000671841.1:n.2477+5_2477+6del
ENST00000671878.1:c.798+5_798+6del	ENSP00000500516.1:n.798+5_798+6del
ENST00000672059.1:n.1249+5_1249+6del
ENST00000672322.1:n.1874_1875del
ENST00000672357.1:c.798+5_798+6del	ENSP00000500092.1:n.798+5_798+6del
ENST00000672465.1:c.798+5_798+6del	ENSP00000500517.1:n.798+5_798+6del
ENST00000672487.1:c.680+1293_680+1294del	ENSP00000500740.1:n.680+1293_680+1294del
ENST00000672564.1:n.1019+5_1019+6del
ENST00000672567.1:c.689+5_689+6del
ENST00000672608.1:n.1787+5_1787+6del
ENST00000672709.1:c.652+5_652+6del
ENST00000673136.1:c.798+5_798+6del	ENSP00000500380.1:n.798+5_798+6del
ENST00000673472.1:n.1134+5_1134+6del
ENST00000176643.10:c.798+5_798+6del	ENSP00000176643.6:n.798+5_798+6del
ENST00000339618.8:c.798+5_798+6del	ENSP00000345774.4:n.798+5_798+6del
ENST00000395575.6:c.798+5_798+6del	ENSP00000378942.2:n.798+5_798+6del
ENST00000472059.5:c.*356+5_*356+6del	ENSP00000458397.1:n.*356+5_*356+6del
ENST00000476965.5:n.548+5_548+6del
ENST00000571537.1:c.291+5_291+6del	ENSP00000458942.1:n.291+5_291+6del
ENST00000578696.1:c.229+5_229+6del
ENST00000579855.5:c.798+5_798+6del	ENSP00000463637.1:n.798+5_798+6del
ENST00000581518.5:c.798+5_798+6del	ENSP00000461916.1:n.798+5_798+6del
ENST00000582991.5:c.798+5_798+6del	ENSP00000464153.1:n.798+5_798+6del
ENST00000630662.2:c.-184+5_-184+6del	ENSP00000487353.1:n.-184+5_-184+6del
ENST00000631291.2:c.798+5_798+6del	ENSP00000486085.1:n.798+5_798+6del
NM_000382.2:c.798+5_798+6del	NP_000373.1:n.798+5_798+6del
NM_001031806.1:c.798+5_798+6del	NP_001026976.1:n.798+5_798+6del
XM_011523732.1:c.798+5_798+6del	XP_011522034.1:n.798+5_798+6del
XM_011523733.1:c.798+5_798+6del	XP_011522035.1:n.798+5_798+6del
XM_011523733.2:c.798+5_798+6del	XP_011522035.1:n.798+5_798+6del
XM_017024355.1:c.798+5_798+6del	XP_016879844.1:n.798+5_798+6del
XM_017024356.2:c.798+5_798+6del	XP_016879845.1:n.798+5_798+6del
XM_017024357.1:c.798+5_798+6del	XP_016879846.1:n.798+5_798+6del
XM_017024358.2:c.798+5_798+6del	XP_016879847.1:n.798+5_798+6del
XM_024450651.1:c.219+5_219+6del	XP_024306419.1:n.219+5_219+6del
XM_024450652.1:c.219+5_219+6del	XP_024306420.1:n.219+5_219+6del
NM_000382.3:c.798+5_798+6del MANE Select	NP_000373.1:n.798+5_798+6del
NM_001031806.2:c.798+5_798+6del	NP_001026976.1:n.798+5_798+6del
NM_001369136.1:c.798+5_798+6del	NP_001356065.1:n.798+5_798+6del
NM_001369137.1:c.798+5_798+6del	NP_001356066.1:n.798+5_798+6del
NM_001369138.1:c.798+5_798+6del	NP_001356067.1:n.798+5_798+6del
NM_001369139.1:c.798+5_798+6del	NP_001356068.1:n.798+5_798+6del
NM_001369146.1:c.798+5_798+6del	NP_001356075.1:n.798+5_798+6del
NM_001369148.1:c.219+5_219+6del	NP_001356077.1:n.219+5_219+6del
NM_001369137.2:c.798+5_798+6del	NP_001356066.1:n.798+5_798+6del
NM_001369138.2:c.798+5_798+6del	NP_001356067.1:n.798+5_798+6del
NM_001369146.2:c.798+5_798+6del	NP_001356075.1:n.798+5_798+6del
NM_001369148.2:c.219+5_219+6del	NP_001356077.1:n.219+5_219+6del