Canonical Allele Identifier: CA362969574
Gene: ALDH5A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1878449
ClinVar RCV Id: RCV002510502

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24503351G>A , CM000668.2:g.24503351G>A GRCh38
NC_000006.11:g.24503579G>A , CM000668.1:g.24503579G>A GRCh37
NC_000006.10:g.24611558G>A NCBI36
NG_008161.1:g.13383G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357578.8:c.527G>A MANE Select ENSP00000350191.3:p.Gly176Glu
ENST00000672352.1:c.290G>A ENSP00000500876.1:p.Gly97Glu
ENST00000672557.1:c.445G>A
ENST00000672652.1:c.448G>A
ENST00000675422.1:n.1287G>A
ENST00000348925.2:c.527G>A ENSP00000314649.3:p.Gly176Glu
ENST00000357578.7:c.527G>A ENSP00000350191.3:p.Gly176Glu
ENST00000491546.5:c.443G>A ENSP00000417687.1:p.Gly148Glu
NM_001080.3:c.527G>A MANE Select NP_001071.1:p.Gly176Glu
NM_170740.1:c.527G>A NP_733936.1:p.Gly176Glu
NM_001368954.1:c.527G>A NP_001355883.1:p.Gly176Glu