Canonical Allele Identifier: CA392790018

Gene: ALDH1A2

Linked Data

• gnomAD v4: 15-58010687-C-T
• MyVariant Identifiers: chr15:g.58302885C>T (hg19) ; chr15:g.58010687C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010687C>T , CM000677.2:g.58010687C>T	GRCh38
NC_000015.9:g.58302885C>T , CM000677.1:g.58302885C>T	GRCh37
NC_000015.8:g.56090177C>T	NCBI36
NG_012259.1:g.60022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.455G>A MANE Select	ENSP00000249750.4:p.Gly152Asp
ENST00000249750.8:c.455G>A	ENSP00000249750.4:p.Gly152Asp
ENST00000347587.7:c.455G>A	ENSP00000309623.3:p.Gly152Asp
ENST00000430119.6:c.*429G>A	ENSP00000416754.2:n.*429G>A
ENST00000537372.5:c.392G>A	ENSP00000438296.1:p.Gly131Asp
ENST00000558231.5:c.368G>A	ENSP00000453600.1:p.Gly123Asp
ENST00000559266.5:n.318+3171G>A
ENST00000559517.5:c.167G>A	ENSP00000453408.1:p.Gly56Asp
ENST00000561070.5:c.167G>A	ENSP00000452850.1:p.Gly56Asp
NM_001206897.1:c.392G>A	NP_001193826.1:p.Gly131Asp
NM_003888.3:c.455G>A	NP_003879.2:p.Gly152Asp
NM_170696.2:c.455G>A	NP_733797.1:p.Gly152Asp
NM_170697.2:c.167G>A	NP_733798.1:p.Gly56Asp
XM_024450095.1:c.455G>A	XP_024305863.1:p.Gly152Asp
NM_003888.4:c.455G>A MANE Select	NP_003879.2:p.Gly152Asp
NM_170696.3:c.455G>A	NP_733797.1:p.Gly152Asp
NM_170697.3:c.167G>A	NP_733798.1:p.Gly56Asp
NM_001206897.2:c.392G>A	NP_001193826.1:p.Gly131Asp