Canonical Allele Identifier: CA2576198602

Gene: ALDH3A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671833_19671837del , CM000679.2:g.19671833_19671837del	GRCh38
NC_000017.10:g.19575146_19575150del , CM000679.1:g.19575146_19575150del	GRCh37
NC_000017.9:g.19515738_19515742del	NCBI36
NG_007095.2:g.28083_28087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1320_1324del MANE Select	ENSP00000176643.6:p.Pro441GlnfsTer?
ENST00000395575.7:c.993_997del	ENSP00000378942.3:p.Pro332GlnfsTer?
ENST00000472059.6:c.*878_*882del	ENSP00000458397.1:n.*878_*882del
ENST00000571163.2:c.227-3663_227-3659del	ENSP00000459977.2:n.227-3663_227-3659del
ENST00000573947.2:c.120_124del	ENSP00000462933.2:p.Pro41GlnfsTer?
ENST00000574078.3:n.649_653del
ENST00000581518.6:c.1320_1324del	ENSP00000461916.2:p.Pro441GlnfsTer?
ENST00000582991.6:c.*38_*42del	ENSP00000464153.1:n.*38_*42del
ENST00000671878.1:c.1320_1324del	ENSP00000500516.1:p.Pro441GlnfsTer?
ENST00000672059.1:n.1671_1675del
ENST00000672357.1:c.1320_1324del	ENSP00000500092.1:p.Pro441GlnfsTer?
ENST00000672465.1:c.1320_1324del	ENSP00000500517.1:p.Pro441GlnfsTer?
ENST00000672487.1:c.*500_*504del	ENSP00000500740.1:n.*500_*504del
ENST00000672564.1:n.2989_2993del
ENST00000672567.1:c.1098+6786_1098+6790del
ENST00000672591.1:c.380_384del
ENST00000672608.1:n.2309_2313del
ENST00000672709.1:c.1174_1178del
ENST00000673064.1:n.1820_1824del
ENST00000673136.1:c.1208-3663_1208-3659del	ENSP00000500380.1:n.1208-3663_1208-3659del
ENST00000673472.1:n.1656_1660del
ENST00000673516.1:n.1780_1784del
ENST00000176643.10:c.1320_1324del	ENSP00000176643.6:p.Pro441GlnfsTer?
ENST00000339618.8:c.1320_1324del	ENSP00000345774.4:p.Pro441GlnfsTer?
ENST00000395575.6:c.1320_1324del	ENSP00000378942.2:p.Pro441GlnfsTer?
ENST00000472059.5:c.*878_*882del	ENSP00000458397.1:n.*878_*882del
ENST00000476965.5:n.1070_1074del
ENST00000571163.1:c.227-3725_227-3721del	ENSP00000459977.1:n.227-3725_227-3721del
ENST00000573565.1:c.35_39del
ENST00000573947.1:c.227_231del	ENSP00000462933.1:n.227_231del
ENST00000575384.2:c.66_70del	ENSP00000461235.2:p.Pro23GlnfsTer?
ENST00000579855.5:c.1320_1324del	ENSP00000463637.1:p.Pro441GlnfsTer?
ENST00000581518.5:c.1320_1324del	ENSP00000461916.1:p.Pro441GlnfsTer?
ENST00000582991.5:c.*38_*42del	ENSP00000464153.1:n.*38_*42del
ENST00000630662.2:c.227-3725_227-3721del	ENSP00000487353.1:n.227-3725_227-3721del
ENST00000631291.2:c.*38_*42del	ENSP00000486085.1:n.*38_*42del
NM_000382.2:c.1320_1324del	NP_000373.1:p.Pro441GlnfsTer?
NM_001031806.1:c.1320_1324del	NP_001026976.1:p.Pro441GlnfsTer?
XM_011523732.1:c.1320_1324del	XP_011522034.1:p.Pro441GlnfsTer?
XM_011523733.1:c.1320_1324del	XP_011522035.1:p.Pro441GlnfsTer?
XM_011523733.2:c.1320_1324del	XP_011522035.1:p.Pro441GlnfsTer?
XM_017024355.1:c.1208-3725_1208-3721del	XP_016879844.1:n.1208-3725_1208-3721del
XM_017024356.2:c.1320_1324del	XP_016879845.1:p.Pro441GlnfsTer?
XM_017024357.1:c.1320_1324del	XP_016879846.1:p.Pro441GlnfsTer?
XM_017024358.2:c.1208-3725_1208-3721del	XP_016879847.1:n.1208-3725_1208-3721del
XM_024450651.1:c.741_745del	XP_024306419.1:p.Pro248GlnfsTer?
XM_024450652.1:c.741_745del	XP_024306420.1:p.Pro248GlnfsTer?
NM_000382.3:c.1320_1324del MANE Select	NP_000373.1:p.Pro441GlnfsTer?
NM_001031806.2:c.1320_1324del	NP_001026976.1:p.Pro441GlnfsTer?
NM_001369136.1:c.1320_1324del	NP_001356065.1:p.Pro441GlnfsTer?
NM_001369137.1:c.1320_1324del	NP_001356066.1:p.Pro441GlnfsTer?
NM_001369138.1:c.1320_1324del	NP_001356067.1:p.Pro441GlnfsTer?
NM_001369139.1:c.1320_1324del	NP_001356068.1:p.Pro441GlnfsTer?
NM_001369146.1:c.1208-3725_1208-3721del	NP_001356075.1:n.1208-3725_1208-3721del
NM_001369148.1:c.741_745del	NP_001356077.1:p.Pro248GlnfsTer?
NM_001369137.2:c.1320_1324del	NP_001356066.1:p.Pro441GlnfsTer?
NM_001369138.2:c.1320_1324del	NP_001356067.1:p.Pro441GlnfsTer?
NM_001369146.2:c.1208-3725_1208-3721del	NP_001356075.1:n.1208-3725_1208-3721del
NM_001369148.2:c.741_745del	NP_001356077.1:p.Pro248GlnfsTer?