Canonical Allele Identifier: CA498619762

Gene: ALDH3A2

Linked Data

• ClinVar Variation Id: 2824698
• ClinVar RCV Id: RCV003678321
• MyVariant Identifiers: chr17:g.19575128T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671815T>G , CM000679.2:g.19671815T>G	GRCh38
NC_000017.10:g.19575128T>G , CM000679.1:g.19575128T>G	GRCh37
NC_000017.9:g.19515720T>G	NCBI36
NG_007095.2:g.28065T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.1302T>G MANE Select	ENSP00000176643.6:p.Gly434=
ENST00000395575.7:c.975T>G	ENSP00000378942.3:p.Gly325=
ENST00000472059.6:c.*860T>G	ENSP00000458397.1:n.*860T>G
ENST00000571163.2:c.227-3681T>G	ENSP00000459977.2:n.227-3681T>G
ENST00000573947.2:c.102T>G	ENSP00000462933.2:p.Gly34=
ENST00000574078.3:n.631T>G
ENST00000581518.6:c.1302T>G	ENSP00000461916.2:p.Gly434=
ENST00000582991.6:c.*20T>G	ENSP00000464153.1:n.*20T>G
ENST00000671878.1:c.1302T>G	ENSP00000500516.1:p.Gly434=
ENST00000672059.1:n.1653T>G
ENST00000672357.1:c.1302T>G	ENSP00000500092.1:p.Gly434=
ENST00000672465.1:c.1302T>G	ENSP00000500517.1:p.Gly434=
ENST00000672487.1:c.*482T>G	ENSP00000500740.1:n.*482T>G
ENST00000672564.1:n.2971T>G
ENST00000672567.1:c.1098+6768T>G
ENST00000672591.1:c.362T>G
ENST00000672608.1:n.2291T>G
ENST00000672709.1:c.1156T>G
ENST00000673064.1:n.1802T>G
ENST00000673136.1:c.1208-3681T>G	ENSP00000500380.1:n.1208-3681T>G
ENST00000673472.1:n.1638T>G
ENST00000673516.1:n.1762T>G
ENST00000176643.10:c.1302T>G	ENSP00000176643.6:p.Gly434=
ENST00000339618.8:c.1302T>G	ENSP00000345774.4:p.Gly434=
ENST00000395575.6:c.1302T>G	ENSP00000378942.2:p.Gly434=
ENST00000472059.5:c.*860T>G	ENSP00000458397.1:n.*860T>G
ENST00000476965.5:n.1052T>G
ENST00000571163.1:c.227-3743T>G	ENSP00000459977.1:n.227-3743T>G
ENST00000573565.1:c.17T>G
ENST00000573947.1:c.209T>G	ENSP00000462933.1:n.209T>G
ENST00000575384.2:c.48T>G	ENSP00000461235.2:p.Gly16=
ENST00000579855.5:c.1302T>G	ENSP00000463637.1:p.Gly434=
ENST00000581518.5:c.1302T>G	ENSP00000461916.1:p.Gly434=
ENST00000582991.5:c.*20T>G	ENSP00000464153.1:n.*20T>G
ENST00000630662.2:c.227-3743T>G	ENSP00000487353.1:n.227-3743T>G
ENST00000631291.2:c.*20T>G	ENSP00000486085.1:n.*20T>G
NM_000382.2:c.1302T>G	NP_000373.1:p.Gly434=
NM_001031806.1:c.1302T>G	NP_001026976.1:p.Gly434=
XM_011523732.1:c.1302T>G	XP_011522034.1:p.Gly434=
XM_011523733.1:c.1302T>G	XP_011522035.1:p.Gly434=
XM_011523733.2:c.1302T>G	XP_011522035.1:p.Gly434=
XM_017024355.1:c.1208-3743T>G	XP_016879844.1:n.1208-3743T>G
XM_017024356.2:c.1302T>G	XP_016879845.1:p.Gly434=
XM_017024357.1:c.1302T>G	XP_016879846.1:p.Gly434=
XM_017024358.2:c.1208-3743T>G	XP_016879847.1:n.1208-3743T>G
XM_024450651.1:c.723T>G	XP_024306419.1:p.Gly241=
XM_024450652.1:c.723T>G	XP_024306420.1:p.Gly241=
NM_000382.3:c.1302T>G MANE Select	NP_000373.1:p.Gly434=
NM_001031806.2:c.1302T>G	NP_001026976.1:p.Gly434=
NM_001369136.1:c.1302T>G	NP_001356065.1:p.Gly434=
NM_001369137.1:c.1302T>G	NP_001356066.1:p.Gly434=
NM_001369138.1:c.1302T>G	NP_001356067.1:p.Gly434=
NM_001369139.1:c.1302T>G	NP_001356068.1:p.Gly434=
NM_001369146.1:c.1208-3743T>G	NP_001356075.1:n.1208-3743T>G
NM_001369148.1:c.723T>G	NP_001356077.1:p.Gly241=
NM_001369137.2:c.1302T>G	NP_001356066.1:p.Gly434=
NM_001369138.2:c.1302T>G	NP_001356067.1:p.Gly434=
NM_001369146.2:c.1208-3743T>G	NP_001356075.1:n.1208-3743T>G
NM_001369148.2:c.723T>G	NP_001356077.1:p.Gly241=