Canonical Allele Identifier: CA136139522

Gene: ALDH5A1

Linked Data

• dbSNP Id: rs986205518
• gnomAD v3: 6-24528314-G-A
• gnomAD v4: 6-24528314-G-A
• MyVariant Identifiers: chr6:g.24528542G>A (hg19) ; chr6:g.24528314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24528314G>A , CM000668.2:g.24528314G>A	GRCh38
NC_000006.11:g.24528542G>A , CM000668.1:g.24528542G>A	GRCh37
NC_000006.10:g.24636521G>A	NCBI36
NG_008161.1:g.38346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357578.8:c.1343+148G>A MANE Select	ENSP00000350191.3:n.1343+148G>A
ENST00000479394.2:n.458+148G>A
ENST00000672352.1:c.962+148G>A	ENSP00000500876.1:n.962+148G>A
ENST00000672652.1:c.1306+148G>A
ENST00000348925.2:c.1382+148G>A	ENSP00000314649.3:n.1382+148G>A
ENST00000357578.7:c.1343+148G>A	ENSP00000350191.3:n.1343+148G>A
ENST00000479394.1:n.458+148G>A
ENST00000491546.5:c.1259+148G>A	ENSP00000417687.1:n.1259+148G>A
NM_001080.3:c.1343+148G>A MANE Select	NP_001071.1:n.1343+148G>A
NM_170740.1:c.1382+148G>A	NP_733936.1:n.1382+148G>A
NM_001368954.1:c.1199+148G>A	NP_001355883.1:n.1199+148G>A