Canonical Allele Identifier: CA565926604

Gene: ALDH5A1

Linked Data

• dbSNP Id: rs1269552614
• gnomAD v2: 6-24503130-T-G
• gnomAD v3: 6-24502902-T-G
• gnomAD v4: 6-24502902-T-G
• MyVariant Identifiers: chr6:g.24503130T>G (hg19) ; chr6:g.24502902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24502902T>G , CM000668.2:g.24502902T>G	GRCh38
NC_000006.11:g.24503130T>G , CM000668.1:g.24503130T>G	GRCh37
NC_000006.10:g.24611109T>G	NCBI36
NG_008161.1:g.12934T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357578.8:c.438+296T>G MANE Select	ENSP00000350191.3:n.438+296T>G
ENST00000672352.1:c.201+296T>G	ENSP00000500876.1:n.201+296T>G
ENST00000672557.1:c.356+139T>G
ENST00000672652.1:c.359+296T>G
ENST00000675422.1:n.1198+296T>G
ENST00000348925.2:c.438+296T>G	ENSP00000314649.3:n.438+296T>G
ENST00000357578.7:c.438+296T>G	ENSP00000350191.3:n.438+296T>G
ENST00000491546.5:c.355-361T>G	ENSP00000417687.1:n.355-361T>G
NM_001080.3:c.438+296T>G MANE Select	NP_001071.1:n.438+296T>G
NM_170740.1:c.438+296T>G	NP_733936.1:n.438+296T>G
NM_001368954.1:c.438+296T>G	NP_001355883.1:n.438+296T>G