Canonical Allele Identifier: CA16041816
Gene: ALDH3A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 370751
ClinVar RCV Id: RCV000411031
dbSNP Id: rs1057516742

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19664946A>G , CM000679.2:g.19664946A>G GRCh38
NC_000017.10:g.19568259A>G , CM000679.1:g.19568259A>G GRCh37
NC_000017.9:g.19508851A>G NCBI36
NG_007095.2:g.21196A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000176643.11:c.1108-2A>G MANE Select ENSP00000176643.6:n.1108-2A>G
ENST00000395575.7:c.781-2A>G ENSP00000378942.3:n.781-2A>G
ENST00000472059.6:c.*666-2A>G ENSP00000458397.1:n.*666-2A>G
ENST00000571163.2:c.127-2A>G ENSP00000459977.2:n.127-2A>G
ENST00000574078.3:n.437-2A>G
ENST00000581518.6:c.1108-2A>G ENSP00000461916.2:n.1108-2A>G
ENST00000582991.6:c.1107+1447A>G ENSP00000464153.1:n.1107+1447A>G
ENST00000671878.1:c.1108-2A>G ENSP00000500516.1:n.1108-2A>G
ENST00000672059.1:n.1558+1447A>G
ENST00000672357.1:c.1108-2A>G ENSP00000500092.1:n.1108-2A>G
ENST00000672465.1:c.1108-2A>G ENSP00000500517.1:n.1108-2A>G
ENST00000672487.1:c.*288-2A>G ENSP00000500740.1:n.*288-2A>G
ENST00000672564.1:n.2775A>G
ENST00000672567.1:c.999-2A>G
ENST00000672591.1:c.168-2A>G
ENST00000672608.1:n.2097-2A>G
ENST00000672709.1:c.962-2A>G
ENST00000673064.1:n.1608-2A>G
ENST00000673136.1:c.1108-2A>G ENSP00000500380.1:n.1108-2A>G
ENST00000673472.1:n.1444-2A>G
ENST00000673516.1:n.1568-2A>G
ENST00000176643.10:c.1108-2A>G ENSP00000176643.6:n.1108-2A>G
ENST00000339618.8:c.1108-2A>G ENSP00000345774.4:n.1108-2A>G
ENST00000395575.6:c.1108-2A>G ENSP00000378942.2:n.1108-2A>G
ENST00000472059.5:c.*666-2A>G ENSP00000458397.1:n.*666-2A>G
ENST00000476965.5:n.858-2A>G
ENST00000571163.1:c.127-2A>G ENSP00000459977.1:n.127-2A>G
ENST00000573947.1:c.114+1447A>G ENSP00000462933.1:n.114+1447A>G
ENST00000579855.5:c.1108-2A>G ENSP00000463637.1:n.1108-2A>G
ENST00000581518.5:c.1108-2A>G ENSP00000461916.1:n.1108-2A>G
ENST00000582991.5:c.1107+1447A>G ENSP00000464153.1:n.1107+1447A>G
ENST00000630662.2:c.127-2A>G ENSP00000487353.1:n.127-2A>G
ENST00000631291.2:c.1107+1447A>G ENSP00000486085.1:n.1107+1447A>G
NM_000382.2:c.1108-2A>G NP_000373.1:n.1108-2A>G
NM_001031806.1:c.1108-2A>G NP_001026976.1:n.1108-2A>G
XM_011523732.1:c.1108-2A>G XP_011522034.1:n.1108-2A>G
XM_011523733.1:c.1108-2A>G XP_011522035.1:n.1108-2A>G
XM_011523733.2:c.1108-2A>G XP_011522035.1:n.1108-2A>G
XM_017024355.1:c.1108-2A>G XP_016879844.1:n.1108-2A>G
XM_017024356.2:c.1108-2A>G XP_016879845.1:n.1108-2A>G
XM_017024357.1:c.1108-2A>G XP_016879846.1:n.1108-2A>G
XM_017024358.2:c.1108-2A>G XP_016879847.1:n.1108-2A>G
XM_024450651.1:c.529-2A>G XP_024306419.1:n.529-2A>G
XM_024450652.1:c.529-2A>G XP_024306420.1:n.529-2A>G
NM_000382.3:c.1108-2A>G MANE Select NP_000373.1:n.1108-2A>G
NM_001031806.2:c.1108-2A>G NP_001026976.1:n.1108-2A>G
NM_001369136.1:c.1108-2A>G NP_001356065.1:n.1108-2A>G
NM_001369137.1:c.1108-2A>G NP_001356066.1:n.1108-2A>G
NM_001369138.1:c.1108-2A>G NP_001356067.1:n.1108-2A>G
NM_001369139.1:c.1108-2A>G NP_001356068.1:n.1108-2A>G
NM_001369146.1:c.1108-2A>G NP_001356075.1:n.1108-2A>G
NM_001369148.1:c.529-2A>G NP_001356077.1:n.529-2A>G
NM_001369137.2:c.1108-2A>G NP_001356066.1:n.1108-2A>G
NM_001369138.2:c.1108-2A>G NP_001356067.1:n.1108-2A>G
NM_001369146.2:c.1108-2A>G NP_001356075.1:n.1108-2A>G
NM_001369148.2:c.529-2A>G NP_001356077.1:n.529-2A>G