Canonical Allele Identifier: CA498619875

Gene: ALDH3A2

Linked Data

• gnomAD v4: 17-19671839-C-T
• MyVariant Identifiers: chr17:g.19575152C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19671839C>T , CM000679.2:g.19671839C>T	GRCh38
NC_000017.10:g.19575152C>T , CM000679.1:g.19575152C>T	GRCh37
NC_000017.9:g.19515744C>T	NCBI36
NG_007095.2:g.28089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.1326C>T MANE Select	ENSP00000176643.6:p.Pro442=
ENST00000395575.7:c.999C>T	ENSP00000378942.3:p.Pro333=
ENST00000472059.6:c.*884C>T	ENSP00000458397.1:n.*884C>T
ENST00000571163.2:c.227-3657C>T	ENSP00000459977.2:n.227-3657C>T
ENST00000573947.2:c.126C>T	ENSP00000462933.2:p.Pro42=
ENST00000574078.3:n.655C>T
ENST00000581518.6:c.1326C>T	ENSP00000461916.2:p.Pro442=
ENST00000582991.6:c.*44C>T	ENSP00000464153.1:n.*44C>T
ENST00000671878.1:c.1326C>T	ENSP00000500516.1:p.Pro442=
ENST00000672059.1:n.1677C>T
ENST00000672357.1:c.1326C>T	ENSP00000500092.1:p.Pro442=
ENST00000672465.1:c.1326C>T	ENSP00000500517.1:p.Pro442=
ENST00000672487.1:c.*506C>T	ENSP00000500740.1:n.*506C>T
ENST00000672564.1:n.2995C>T
ENST00000672567.1:c.1098+6792C>T
ENST00000672591.1:c.386C>T
ENST00000672608.1:n.2315C>T
ENST00000672709.1:c.1180C>T
ENST00000673064.1:n.1826C>T
ENST00000673136.1:c.1208-3657C>T	ENSP00000500380.1:n.1208-3657C>T
ENST00000673472.1:n.1662C>T
ENST00000673516.1:n.1786C>T
ENST00000176643.10:c.1326C>T	ENSP00000176643.6:p.Pro442=
ENST00000339618.8:c.1326C>T	ENSP00000345774.4:p.Pro442=
ENST00000395575.6:c.1326C>T	ENSP00000378942.2:p.Pro442=
ENST00000472059.5:c.*884C>T	ENSP00000458397.1:n.*884C>T
ENST00000476965.5:n.1076C>T
ENST00000571163.1:c.227-3719C>T	ENSP00000459977.1:n.227-3719C>T
ENST00000573565.1:c.41C>T
ENST00000573947.1:c.233C>T	ENSP00000462933.1:n.233C>T
ENST00000575384.2:c.72C>T	ENSP00000461235.2:p.Pro24=
ENST00000579855.5:c.1326C>T	ENSP00000463637.1:p.Pro442=
ENST00000581518.5:c.1326C>T	ENSP00000461916.1:p.Pro442=
ENST00000582991.5:c.*44C>T	ENSP00000464153.1:n.*44C>T
ENST00000630662.2:c.227-3719C>T	ENSP00000487353.1:n.227-3719C>T
ENST00000631291.2:c.*44C>T	ENSP00000486085.1:n.*44C>T
NM_000382.2:c.1326C>T	NP_000373.1:p.Pro442=
NM_001031806.1:c.1326C>T	NP_001026976.1:p.Pro442=
XM_011523732.1:c.1326C>T	XP_011522034.1:p.Pro442=
XM_011523733.1:c.1326C>T	XP_011522035.1:p.Pro442=
XM_011523733.2:c.1326C>T	XP_011522035.1:p.Pro442=
XM_017024355.1:c.1208-3719C>T	XP_016879844.1:n.1208-3719C>T
XM_017024356.2:c.1326C>T	XP_016879845.1:p.Pro442=
XM_017024357.1:c.1326C>T	XP_016879846.1:p.Pro442=
XM_017024358.2:c.1208-3719C>T	XP_016879847.1:n.1208-3719C>T
XM_024450651.1:c.747C>T	XP_024306419.1:p.Pro249=
XM_024450652.1:c.747C>T	XP_024306420.1:p.Pro249=
NM_000382.3:c.1326C>T MANE Select	NP_000373.1:p.Pro442=
NM_001031806.2:c.1326C>T	NP_001026976.1:p.Pro442=
NM_001369136.1:c.1326C>T	NP_001356065.1:p.Pro442=
NM_001369137.1:c.1326C>T	NP_001356066.1:p.Pro442=
NM_001369138.1:c.1326C>T	NP_001356067.1:p.Pro442=
NM_001369139.1:c.1326C>T	NP_001356068.1:p.Pro442=
NM_001369146.1:c.1208-3719C>T	NP_001356075.1:n.1208-3719C>T
NM_001369148.1:c.747C>T	NP_001356077.1:p.Pro249=
NM_001369137.2:c.1326C>T	NP_001356066.1:p.Pro442=
NM_001369138.2:c.1326C>T	NP_001356067.1:p.Pro442=
NM_001369146.2:c.1208-3719C>T	NP_001356075.1:n.1208-3719C>T
NM_001369148.2:c.747C>T	NP_001356077.1:p.Pro249=