Canonical Allele Identifier: CA398701801

Gene: ALDH3A2

Linked Data

• MyVariant Identifiers: chr17:g.19554939G>C (hg19) ; chr17:g.19651626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19651626G>C , CM000679.2:g.19651626G>C	GRCh38
NC_000017.10:g.19554939G>C , CM000679.1:g.19554939G>C	GRCh37
NC_000017.9:g.19495531G>C	NCBI36
NG_007095.2:g.7876G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.233G>C MANE Select	ENSP00000176643.6:p.Trp78Ser
ENST00000395575.7:c.233G>C	ENSP00000378942.3:p.Trp78Ser
ENST00000446398.7:n.243G>C
ENST00000467473.6:n.356G>C
ENST00000472059.6:c.233G>C	ENSP00000458397.1:p.Trp78Ser
ENST00000581518.6:c.233G>C	ENSP00000461916.2:p.Trp78Ser
ENST00000582991.6:c.233G>C	ENSP00000464153.1:p.Trp78Ser
ENST00000671878.1:c.233G>C	ENSP00000500516.1:p.Trp78Ser
ENST00000672357.1:c.233G>C	ENSP00000500092.1:p.Trp78Ser
ENST00000672465.1:c.233G>C	ENSP00000500517.1:p.Trp78Ser
ENST00000672487.1:c.233G>C	ENSP00000500740.1:p.Trp78Ser
ENST00000672564.1:n.454G>C
ENST00000672567.1:c.124G>C
ENST00000672709.1:c.87G>C
ENST00000673136.1:c.233G>C	ENSP00000500380.1:p.Trp78Ser
ENST00000176643.10:c.233G>C	ENSP00000176643.6:p.Trp78Ser
ENST00000339618.8:c.233G>C	ENSP00000345774.4:p.Trp78Ser
ENST00000395575.6:c.233G>C	ENSP00000378942.2:p.Trp78Ser
ENST00000446398.6:c.233G>C	ENSP00000395845.2:p.Trp78Ser
ENST00000467473.5:n.390G>C
ENST00000472059.5:c.233G>C	ENSP00000458397.1:p.Trp78Ser
ENST00000578614.1:c.154-921G>C	ENSP00000463128.1:n.154-921G>C
ENST00000579403.1:n.279G>C
ENST00000579855.5:c.233G>C	ENSP00000463637.1:p.Trp78Ser
ENST00000580550.5:c.233G>C	ENSP00000462964.1:p.Trp78Ser
ENST00000581518.5:c.233G>C	ENSP00000461916.1:p.Trp78Ser
ENST00000582991.5:c.233G>C	ENSP00000464153.1:p.Trp78Ser
ENST00000584332.6:c.137G>C	ENSP00000466814.1:p.Trp46Ser
ENST00000626500.2:c.233G>C	ENSP00000486283.1:p.Trp78Ser
ENST00000630662.2:c.-749G>C	ENSP00000487353.1:n.-749G>C
ENST00000631291.2:c.233G>C	ENSP00000486085.1:p.Trp78Ser
NM_000382.2:c.233G>C	NP_000373.1:p.Trp78Ser
NM_001031806.1:c.233G>C	NP_001026976.1:p.Trp78Ser
XM_011523732.1:c.233G>C	XP_011522034.1:p.Trp78Ser
XM_011523733.1:c.233G>C	XP_011522035.1:p.Trp78Ser
XM_011523733.2:c.233G>C	XP_011522035.1:p.Trp78Ser
XM_017024355.1:c.233G>C	XP_016879844.1:p.Trp78Ser
XM_017024356.2:c.233G>C	XP_016879845.1:p.Trp78Ser
XM_017024357.1:c.233G>C	XP_016879846.1:p.Trp78Ser
XM_017024358.2:c.233G>C	XP_016879847.1:p.Trp78Ser
XM_024450651.1:c.-456G>C	XP_024306419.1:n.-456G>C
XM_024450652.1:c.-456G>C	XP_024306420.1:n.-456G>C
NM_000382.3:c.233G>C MANE Select	NP_000373.1:p.Trp78Ser
NM_001031806.2:c.233G>C	NP_001026976.1:p.Trp78Ser
NM_001369136.1:c.233G>C	NP_001356065.1:p.Trp78Ser
NM_001369137.1:c.233G>C	NP_001356066.1:p.Trp78Ser
NM_001369138.1:c.233G>C	NP_001356067.1:p.Trp78Ser
NM_001369139.1:c.233G>C	NP_001356068.1:p.Trp78Ser
NM_001369146.1:c.233G>C	NP_001356075.1:p.Trp78Ser
NM_001369148.1:c.-456G>C	NP_001356077.1:n.-456G>C
NM_001369137.2:c.233G>C	NP_001356066.1:p.Trp78Ser
NM_001369138.2:c.233G>C	NP_001356067.1:p.Trp78Ser
NM_001369146.2:c.233G>C	NP_001356075.1:p.Trp78Ser
NM_001369148.2:c.-456G>C	NP_001356077.1:n.-456G>C