Canonical Allele Identifier: CA115112
Gene: ALDH3A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1637
ClinVar RCV Id: RCV000001704
dbSNP Id: rs387906255

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19661137del , CM000679.2:g.19661137del GRCh38
NC_000017.10:g.19564450del , CM000679.1:g.19564450del GRCh37
NC_000017.9:g.19505042del NCBI36
NG_007095.2:g.17387del

Transcript Alleles

HGVS Amino-acid change
ENST00000176643.11:c.809del MANE Select ENSP00000176643.6:p.Gly270GlufsTer4
ENST00000395575.7:c.482del ENSP00000378942.3:p.Gly161GlufsTer4
ENST00000472059.6:c.*367del ENSP00000458397.1:n.*367del
ENST00000574078.3:n.138del
ENST00000581518.6:c.809del ENSP00000461916.2:p.Gly270GlufsTer4
ENST00000582991.6:c.809del ENSP00000464153.1:p.Gly270GlufsTer4
ENST00000671841.1:n.2488del
ENST00000671878.1:c.809del ENSP00000500516.1:p.Gly270GlufsTer4
ENST00000672059.1:n.1260del
ENST00000672357.1:c.809del ENSP00000500092.1:p.Gly270GlufsTer4
ENST00000672465.1:c.809del ENSP00000500517.1:p.Gly270GlufsTer4
ENST00000672487.1:c.691del ENSP00000500740.1:p.Glu231ArgfsTer8
ENST00000672564.1:n.1030del
ENST00000672567.1:c.700del
ENST00000672608.1:n.1798del
ENST00000672709.1:c.663del
ENST00000673064.1:n.1309del
ENST00000673136.1:c.809del ENSP00000500380.1:p.Gly270GlufsTer4
ENST00000673472.1:n.1145del
ENST00000673516.1:n.1269del
ENST00000176643.10:c.809del ENSP00000176643.6:p.Gly270GlufsTer4
ENST00000339618.8:c.809del ENSP00000345774.4:p.Gly270GlufsTer4
ENST00000395575.6:c.809del ENSP00000378942.2:p.Gly270GlufsTer4
ENST00000472059.5:c.*367del ENSP00000458397.1:n.*367del
ENST00000476965.5:n.559del
ENST00000571537.1:c.302del ENSP00000458942.1:p.Gly101GlufsTer4
ENST00000574078.2:n.138del
ENST00000578696.1:c.240del
ENST00000579855.5:c.809del ENSP00000463637.1:p.Gly270GlufsTer4
ENST00000581518.5:c.809del ENSP00000461916.1:p.Gly270GlufsTer4
ENST00000582991.5:c.809del ENSP00000464153.1:p.Gly270GlufsTer4
ENST00000630662.2:c.-173del ENSP00000487353.1:n.-173del
ENST00000631291.2:c.809del ENSP00000486085.1:p.Gly270GlufsTer4
NM_000382.2:c.809del NP_000373.1:p.Gly270GlufsTer4
NM_001031806.1:c.809del NP_001026976.1:p.Gly270GlufsTer4
XM_011523732.1:c.809del XP_011522034.1:p.Gly270GlufsTer4
XM_011523733.1:c.809del XP_011522035.1:p.Gly270GlufsTer4
XM_011523733.2:c.809del XP_011522035.1:p.Gly270GlufsTer4
XM_017024355.1:c.809del XP_016879844.1:p.Gly270GlufsTer4
XM_017024356.2:c.809del XP_016879845.1:p.Gly270GlufsTer4
XM_017024357.1:c.809del XP_016879846.1:p.Gly270GlufsTer4
XM_017024358.2:c.809del XP_016879847.1:p.Gly270GlufsTer4
XM_024450651.1:c.230del XP_024306419.1:p.Gly77GlufsTer4
XM_024450652.1:c.230del XP_024306420.1:p.Gly77GlufsTer4
NM_000382.3:c.809del MANE Select NP_000373.1:p.Gly270GlufsTer4
NM_001031806.2:c.809del NP_001026976.1:p.Gly270GlufsTer4
NM_001369136.1:c.809del NP_001356065.1:p.Gly270GlufsTer4
NM_001369137.1:c.809del NP_001356066.1:p.Gly270GlufsTer4
NM_001369138.1:c.809del NP_001356067.1:p.Gly270GlufsTer4
NM_001369139.1:c.809del NP_001356068.1:p.Gly270GlufsTer4
NM_001369146.1:c.809del NP_001356075.1:p.Gly270GlufsTer4
NM_001369148.1:c.230del NP_001356077.1:p.Gly77GlufsTer4
NM_001369137.2:c.809del NP_001356066.1:p.Gly270GlufsTer4
NM_001369138.2:c.809del NP_001356067.1:p.Gly270GlufsTer4
NM_001369146.2:c.809del NP_001356075.1:p.Gly270GlufsTer4
NM_001369148.2:c.230del NP_001356077.1:p.Gly77GlufsTer4