Canonical Allele Identifier: CA498620006

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19575185T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671872T>C , CM000679.2:g.19671872T>C	GRCh38
NC_000017.10:g.19575185T>C , CM000679.1:g.19575185T>C	GRCh37
NC_000017.9:g.19515777T>C	NCBI36
NG_007095.2:g.28122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1359T>C MANE Select	ENSP00000176643.6:p.Phe453=
ENST00000395575.7:c.1032T>C	ENSP00000378942.3:p.Phe344=
ENST00000472059.6:c.*917T>C	ENSP00000458397.1:n.*917T>C
ENST00000571163.2:c.227-3624T>C	ENSP00000459977.2:n.227-3624T>C
ENST00000573947.2:c.159T>C	ENSP00000462933.2:p.Phe53=
ENST00000574078.3:n.688T>C
ENST00000581518.6:c.1359T>C	ENSP00000461916.2:p.Phe453=
ENST00000582991.6:c.*77T>C	ENSP00000464153.1:n.*77T>C
ENST00000671878.1:c.1359T>C	ENSP00000500516.1:p.Phe453=
ENST00000672059.1:n.1710T>C
ENST00000672357.1:c.1359T>C	ENSP00000500092.1:p.Phe453=
ENST00000672465.1:c.1359T>C	ENSP00000500517.1:p.Phe453=
ENST00000672487.1:c.*539T>C	ENSP00000500740.1:n.*539T>C
ENST00000672564.1:n.3028T>C
ENST00000672567.1:c.1098+6825T>C
ENST00000672591.1:c.419T>C
ENST00000672608.1:n.2348T>C
ENST00000672709.1:c.1213T>C
ENST00000673064.1:n.1859T>C
ENST00000673136.1:c.1208-3624T>C	ENSP00000500380.1:n.1208-3624T>C
ENST00000673472.1:n.1695T>C
ENST00000673516.1:n.1819T>C
ENST00000176643.10:c.1359T>C	ENSP00000176643.6:p.Phe453=
ENST00000339618.8:c.1359T>C	ENSP00000345774.4:p.Phe453=
ENST00000395575.6:c.1359T>C	ENSP00000378942.2:p.Phe453=
ENST00000472059.5:c.*917T>C	ENSP00000458397.1:n.*917T>C
ENST00000476965.5:n.1109T>C
ENST00000571163.1:c.227-3686T>C	ENSP00000459977.1:n.227-3686T>C
ENST00000573565.1:c.74T>C
ENST00000573947.1:c.266T>C	ENSP00000462933.1:n.266T>C
ENST00000575384.2:c.105T>C	ENSP00000461235.2:p.Phe35=
ENST00000579855.5:c.1359T>C	ENSP00000463637.1:p.Phe453=
ENST00000581518.5:c.1359T>C	ENSP00000461916.1:p.Phe453=
ENST00000582991.5:c.*77T>C	ENSP00000464153.1:n.*77T>C
ENST00000630662.2:c.227-3686T>C	ENSP00000487353.1:n.227-3686T>C
ENST00000631291.2:c.*77T>C	ENSP00000486085.1:n.*77T>C
NM_000382.2:c.1359T>C	NP_000373.1:p.Phe453=
NM_001031806.1:c.1359T>C	NP_001026976.1:p.Phe453=
XM_011523732.1:c.1359T>C	XP_011522034.1:p.Phe453=
XM_011523733.1:c.1359T>C	XP_011522035.1:p.Phe453=
XM_011523733.2:c.1359T>C	XP_011522035.1:p.Phe453=
XM_017024355.1:c.1208-3686T>C	XP_016879844.1:n.1208-3686T>C
XM_017024356.2:c.1359T>C	XP_016879845.1:p.Phe453=
XM_017024357.1:c.1359T>C	XP_016879846.1:p.Phe453=
XM_017024358.2:c.1208-3686T>C	XP_016879847.1:n.1208-3686T>C
XM_024450651.1:c.780T>C	XP_024306419.1:p.Phe260=
XM_024450652.1:c.780T>C	XP_024306420.1:p.Phe260=
NM_000382.3:c.1359T>C MANE Select	NP_000373.1:p.Phe453=
NM_001031806.2:c.1359T>C	NP_001026976.1:p.Phe453=
NM_001369136.1:c.1359T>C	NP_001356065.1:p.Phe453=
NM_001369137.1:c.1359T>C	NP_001356066.1:p.Phe453=
NM_001369138.1:c.1359T>C	NP_001356067.1:p.Phe453=
NM_001369139.1:c.1359T>C	NP_001356068.1:p.Phe453=
NM_001369146.1:c.1208-3686T>C	NP_001356075.1:n.1208-3686T>C
NM_001369148.1:c.780T>C	NP_001356077.1:p.Phe260=
NM_001369137.2:c.1359T>C	NP_001356066.1:p.Phe453=
NM_001369138.2:c.1359T>C	NP_001356067.1:p.Phe453=
NM_001369146.2:c.1208-3686T>C	NP_001356075.1:n.1208-3686T>C
NM_001369148.2:c.780T>C	NP_001356077.1:p.Phe260=