Canonical Allele Identifier: CA2733202251

Gene: ALDH3A2

Linked Data

• dbSNP Id: rs3034928

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19657708_19657715dup , CM000679.2:g.19657708_19657715dup	GRCh38
NC_000017.10:g.19561021_19561028dup , CM000679.1:g.19561021_19561028dup	GRCh37
NC_000017.9:g.19501613_19501620dup	NCBI36
NG_007095.2:g.13958_13965dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.681-37_681-30dup MANE Select	ENSP00000176643.6:n.681-37_681-30dup
ENST00000395575.7:c.472-3419_472-3412dup	ENSP00000378942.3:n.472-3419_472-3412dup
ENST00000472059.6:c.*239-37_*239-30dup	ENSP00000458397.1:n.*239-37_*239-30dup
ENST00000581518.6:c.681-37_681-30dup	ENSP00000461916.2:n.681-37_681-30dup
ENST00000582991.6:c.681-37_681-30dup	ENSP00000464153.1:n.681-37_681-30dup
ENST00000671841.1:n.2323_2330dup
ENST00000671878.1:c.681-37_681-30dup	ENSP00000500516.1:n.681-37_681-30dup
ENST00000672059.1:n.1132-37_1132-30dup
ENST00000672322.1:n.1752-37_1752-30dup
ENST00000672357.1:c.681-37_681-30dup	ENSP00000500092.1:n.681-37_681-30dup
ENST00000672465.1:c.681-37_681-30dup	ENSP00000500517.1:n.681-37_681-30dup
ENST00000672487.1:c.680+1134_680+1141dup	ENSP00000500740.1:n.680+1134_680+1141dup
ENST00000672564.1:n.902-37_902-30dup
ENST00000672567.1:c.572-37_572-30dup
ENST00000672608.1:n.1670-37_1670-30dup
ENST00000672709.1:c.535-37_535-30dup
ENST00000673136.1:c.681-37_681-30dup	ENSP00000500380.1:n.681-37_681-30dup
ENST00000673472.1:n.1017-37_1017-30dup
ENST00000176643.10:c.681-37_681-30dup	ENSP00000176643.6:n.681-37_681-30dup
ENST00000339618.8:c.681-37_681-30dup	ENSP00000345774.4:n.681-37_681-30dup
ENST00000395575.6:c.681-37_681-30dup	ENSP00000378942.2:n.681-37_681-30dup
ENST00000472059.5:c.*239-37_*239-30dup	ENSP00000458397.1:n.*239-37_*239-30dup
ENST00000476965.5:n.431-37_431-30dup
ENST00000571537.1:c.174-37_174-30dup	ENSP00000458942.1:n.174-37_174-30dup
ENST00000578696.1:c.88-13_88-6dup
ENST00000579855.5:c.681-37_681-30dup	ENSP00000463637.1:n.681-37_681-30dup
ENST00000581518.5:c.681-37_681-30dup	ENSP00000461916.1:n.681-37_681-30dup
ENST00000582991.5:c.681-37_681-30dup	ENSP00000464153.1:n.681-37_681-30dup
ENST00000630662.2:c.-301-37_-301-30dup	ENSP00000487353.1:n.-301-37_-301-30dup
ENST00000631291.2:c.681-37_681-30dup	ENSP00000486085.1:n.681-37_681-30dup
NM_000382.2:c.681-37_681-30dup	NP_000373.1:n.681-37_681-30dup
NM_001031806.1:c.681-37_681-30dup	NP_001026976.1:n.681-37_681-30dup
XM_011523732.1:c.681-37_681-30dup	XP_011522034.1:n.681-37_681-30dup
XM_011523733.1:c.681-37_681-30dup	XP_011522035.1:n.681-37_681-30dup
XM_011523733.2:c.681-37_681-30dup	XP_011522035.1:n.681-37_681-30dup
XM_017024355.1:c.681-37_681-30dup	XP_016879844.1:n.681-37_681-30dup
XM_017024356.2:c.681-37_681-30dup	XP_016879845.1:n.681-37_681-30dup
XM_017024357.1:c.681-37_681-30dup	XP_016879846.1:n.681-37_681-30dup
XM_017024358.2:c.681-37_681-30dup	XP_016879847.1:n.681-37_681-30dup
XM_024450651.1:c.102-37_102-30dup	XP_024306419.1:n.102-37_102-30dup
XM_024450652.1:c.102-37_102-30dup	XP_024306420.1:n.102-37_102-30dup
NM_000382.3:c.681-37_681-30dup MANE Select	NP_000373.1:n.681-37_681-30dup
NM_001031806.2:c.681-37_681-30dup	NP_001026976.1:n.681-37_681-30dup
NM_001369136.1:c.681-37_681-30dup	NP_001356065.1:n.681-37_681-30dup
NM_001369137.1:c.681-37_681-30dup	NP_001356066.1:n.681-37_681-30dup
NM_001369138.1:c.681-37_681-30dup	NP_001356067.1:n.681-37_681-30dup
NM_001369139.1:c.681-37_681-30dup	NP_001356068.1:n.681-37_681-30dup
NM_001369146.1:c.681-37_681-30dup	NP_001356075.1:n.681-37_681-30dup
NM_001369148.1:c.102-37_102-30dup	NP_001356077.1:n.102-37_102-30dup
NM_001369137.2:c.681-37_681-30dup	NP_001356066.1:n.681-37_681-30dup
NM_001369138.2:c.681-37_681-30dup	NP_001356067.1:n.681-37_681-30dup
NM_001369146.2:c.681-37_681-30dup	NP_001356075.1:n.681-37_681-30dup
NM_001369148.2:c.102-37_102-30dup	NP_001356077.1:n.102-37_102-30dup