Canonical Allele Identifier: CA136139117

Gene: ALDH5A1

Linked Data

• dbSNP Id: rs1003481278
• gnomAD v3: 6-24527827-T-C
• gnomAD v4: 6-24527827-T-C
• MyVariant Identifiers: chr6:g.24528055T>C (hg19) ; chr6:g.24527827T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24527827T>C , CM000668.2:g.24527827T>C	GRCh38
NC_000006.11:g.24528055T>C , CM000668.1:g.24528055T>C	GRCh37
NC_000006.10:g.24636034T>C	NCBI36
NG_008161.1:g.37859T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357578.8:c.1174-170T>C MANE Select	ENSP00000350191.3:n.1174-170T>C
ENST00000479394.2:n.289-170T>C
ENST00000672352.1:c.793-170T>C	ENSP00000500876.1:n.793-170T>C
ENST00000672652.1:c.1137-170T>C
ENST00000348925.2:c.1213-170T>C	ENSP00000314649.3:n.1213-170T>C
ENST00000357578.7:c.1174-170T>C	ENSP00000350191.3:n.1174-170T>C
ENST00000479394.1:n.289-170T>C
ENST00000491546.5:c.1090-170T>C	ENSP00000417687.1:n.1090-170T>C
NM_001080.3:c.1174-170T>C MANE Select	NP_001071.1:n.1174-170T>C
NM_170740.1:c.1213-170T>C	NP_733936.1:n.1213-170T>C
NM_001368954.1:c.1030-170T>C	NP_001355883.1:n.1030-170T>C