Canonical Allele Identifier: CA8442894

Gene: ALDH3A2

Linked Data

• dbSNP Id: rs758618354
• ExAC: 17:19561077 T / C
• gnomAD v2: 17-19561077-T-C
• gnomAD v3: 17-19657764-T-C
• gnomAD v4: 17-19657764-T-C
• MyVariant Identifiers: chr17:g.19561077T>C (hg19) ; chr17:g.19657764T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19657764T>C , CM000679.2:g.19657764T>C	GRCh38
NC_000017.10:g.19561077T>C , CM000679.1:g.19561077T>C	GRCh37
NC_000017.9:g.19501669T>C	NCBI36
NG_007095.2:g.14014T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.700T>C MANE Select	ENSP00000176643.6:p.Tyr234His
ENST00000395575.7:c.472-3363T>C	ENSP00000378942.3:n.472-3363T>C
ENST00000472059.6:c.*258T>C	ENSP00000458397.1:n.*258T>C
ENST00000581518.6:c.700T>C	ENSP00000461916.2:p.Tyr234His
ENST00000582991.6:c.700T>C	ENSP00000464153.1:p.Tyr234His
ENST00000671841.1:n.2379T>C
ENST00000671878.1:c.700T>C	ENSP00000500516.1:p.Tyr234His
ENST00000672059.1:n.1151T>C
ENST00000672322.1:n.1771T>C
ENST00000672357.1:c.700T>C	ENSP00000500092.1:p.Tyr234His
ENST00000672465.1:c.700T>C	ENSP00000500517.1:p.Tyr234His
ENST00000672487.1:c.680+1190T>C	ENSP00000500740.1:n.680+1190T>C
ENST00000672564.1:n.921T>C
ENST00000672567.1:c.591T>C
ENST00000672608.1:n.1689T>C
ENST00000672709.1:c.554T>C
ENST00000673136.1:c.700T>C	ENSP00000500380.1:p.Tyr234His
ENST00000673472.1:n.1036T>C
ENST00000176643.10:c.700T>C	ENSP00000176643.6:p.Tyr234His
ENST00000339618.8:c.700T>C	ENSP00000345774.4:p.Tyr234His
ENST00000395575.6:c.700T>C	ENSP00000378942.2:p.Tyr234His
ENST00000472059.5:c.*258T>C	ENSP00000458397.1:n.*258T>C
ENST00000476965.5:n.450T>C
ENST00000571537.1:c.193T>C	ENSP00000458942.1:p.Tyr65His
ENST00000578696.1:c.131T>C
ENST00000579855.5:c.700T>C	ENSP00000463637.1:p.Tyr234His
ENST00000581518.5:c.700T>C	ENSP00000461916.1:p.Tyr234His
ENST00000582991.5:c.700T>C	ENSP00000464153.1:p.Tyr234His
ENST00000630662.2:c.-282T>C	ENSP00000487353.1:n.-282T>C
ENST00000631291.2:c.700T>C	ENSP00000486085.1:p.Tyr234His
NM_000382.2:c.700T>C	NP_000373.1:p.Tyr234His
NM_001031806.1:c.700T>C	NP_001026976.1:p.Tyr234His
XM_011523732.1:c.700T>C	XP_011522034.1:p.Tyr234His
XM_011523733.1:c.700T>C	XP_011522035.1:p.Tyr234His
XM_011523733.2:c.700T>C	XP_011522035.1:p.Tyr234His
XM_017024355.1:c.700T>C	XP_016879844.1:p.Tyr234His
XM_017024356.2:c.700T>C	XP_016879845.1:p.Tyr234His
XM_017024357.1:c.700T>C	XP_016879846.1:p.Tyr234His
XM_017024358.2:c.700T>C	XP_016879847.1:p.Tyr234His
XM_024450651.1:c.121T>C	XP_024306419.1:p.Tyr41His
XM_024450652.1:c.121T>C	XP_024306420.1:p.Tyr41His
NM_000382.3:c.700T>C MANE Select	NP_000373.1:p.Tyr234His
NM_001031806.2:c.700T>C	NP_001026976.1:p.Tyr234His
NM_001369136.1:c.700T>C	NP_001356065.1:p.Tyr234His
NM_001369137.1:c.700T>C	NP_001356066.1:p.Tyr234His
NM_001369138.1:c.700T>C	NP_001356067.1:p.Tyr234His
NM_001369139.1:c.700T>C	NP_001356068.1:p.Tyr234His
NM_001369146.1:c.700T>C	NP_001356075.1:p.Tyr234His
NM_001369148.1:c.121T>C	NP_001356077.1:p.Tyr41His
NM_001369137.2:c.700T>C	NP_001356066.1:p.Tyr234His
NM_001369138.2:c.700T>C	NP_001356067.1:p.Tyr234His
NM_001369146.2:c.700T>C	NP_001356075.1:p.Tyr234His
NM_001369148.2:c.121T>C	NP_001356077.1:p.Tyr41His