Canonical Allele Identifier: CA2636595829
Gene: ALDH3A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19648738T>G , CM000679.2:g.19648738T>G GRCh38
NC_000017.10:g.19552051T>G , CM000679.1:g.19552051T>G GRCh37
NC_000017.9:g.19492643T>G NCBI36
NG_007095.2:g.4988T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467473.6:n.87-197T>G
ENST00000581518.6:c.-37-197T>G ENSP00000461916.2:n.-37-197T>G
ENST00000672357.1:c.-143T>G ENSP00000500092.1:n.-143T>G
ENST00000672465.1:c.-37-197T>G ENSP00000500517.1:n.-37-197T>G
ENST00000673136.1:c.-37-197T>G ENSP00000500380.1:n.-37-197T>G
ENST00000176643.10:c.-234T>G ENSP00000176643.6:n.-234T>G
ENST00000395575.6:c.-143T>G ENSP00000378942.2:n.-143T>G
ENST00000446398.6:c.-37-197T>G ENSP00000395845.2:n.-37-197T>G
ENST00000467473.5:n.121-197T>G
ENST00000580550.5:c.-9-225T>G ENSP00000462964.1:n.-9-225T>G
ENST00000581518.5:c.-234T>G ENSP00000461916.1:n.-234T>G
ENST00000582991.5:c.-234T>G ENSP00000464153.1:n.-234T>G
ENST00000626500.2:c.-234T>G ENSP00000486283.1:n.-234T>G
ENST00000631291.2:c.-234T>G ENSP00000486085.1:n.-234T>G
XM_011523733.1:c.-37-197T>G XP_011522035.1:n.-37-197T>G
XM_011523733.2:c.-37-197T>G XP_011522035.1:n.-37-197T>G
XM_017024356.2:c.-37-197T>G XP_016879845.1:n.-37-197T>G
XM_017024358.2:c.-37-197T>G XP_016879847.1:n.-37-197T>G
XM_024450652.1:c.-725-197T>G XP_024306420.1:n.-725-197T>G
NM_001369137.1:c.-37-197T>G NP_001356066.1:n.-37-197T>G
NM_001369138.1:c.-37-197T>G NP_001356067.1:n.-37-197T>G
NM_001369146.1:c.-37-197T>G NP_001356075.1:n.-37-197T>G
NM_001369148.1:c.-725-197T>G NP_001356077.1:n.-725-197T>G
NM_001369137.2:c.-37-197T>G NP_001356066.1:n.-37-197T>G
NM_001369138.2:c.-37-197T>G NP_001356067.1:n.-37-197T>G
NM_001369146.2:c.-37-197T>G NP_001356075.1:n.-37-197T>G
NM_001369148.2:c.-725-197T>G NP_001356077.1:n.-725-197T>G