Canonical Allele Identifier: CA362969591

Gene: ALDH5A1

Linked Data

• ClinVar Variation Id: 904147
• ClinVar RCV Id: RCV001151890
• dbSNP Id: rs1759245914
• gnomAD v3: 6-24503359-A-G
• gnomAD v4: 6-24503359-A-G
• MyVariant Identifiers: chr6:g.24503587A>G (hg19) ; chr6:g.24503359A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24503359A>G , CM000668.2:g.24503359A>G	GRCh38
NC_000006.11:g.24503587A>G , CM000668.1:g.24503587A>G	GRCh37
NC_000006.10:g.24611566A>G	NCBI36
NG_008161.1:g.13391A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357578.8:c.535A>G MANE Select	ENSP00000350191.3:p.Ile179Val
ENST00000672352.1:c.298A>G	ENSP00000500876.1:p.Ile100Val
ENST00000672557.1:c.453A>G
ENST00000672652.1:c.456A>G
ENST00000675422.1:n.1295A>G
ENST00000348925.2:c.535A>G	ENSP00000314649.3:p.Ile179Val
ENST00000357578.7:c.535A>G	ENSP00000350191.3:p.Ile179Val
ENST00000491546.5:c.451A>G	ENSP00000417687.1:p.Ile151Val
NM_001080.3:c.535A>G MANE Select	NP_001071.1:p.Ile179Val
NM_170740.1:c.535A>G	NP_733936.1:p.Ile179Val
NM_001368954.1:c.535A>G	NP_001355883.1:p.Ile179Val