Canonical Allele Identifier: CA392789966

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302876T>A (hg19) ; chr15:g.58010678T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010678T>A , CM000677.2:g.58010678T>A	GRCh38
NC_000015.9:g.58302876T>A , CM000677.1:g.58302876T>A	GRCh37
NC_000015.8:g.56090168T>A	NCBI36
NG_012259.1:g.60031A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.464A>T MANE Select	ENSP00000249750.4:p.Asp155Val
ENST00000249750.8:c.464A>T	ENSP00000249750.4:p.Asp155Val
ENST00000347587.7:c.464A>T	ENSP00000309623.3:p.Asp155Val
ENST00000430119.6:c.*438A>T	ENSP00000416754.2:n.*438A>T
ENST00000537372.5:c.401A>T	ENSP00000438296.1:p.Asp134Val
ENST00000558231.5:c.377A>T	ENSP00000453600.1:p.Asp126Val
ENST00000559266.5:n.318+3180A>T
ENST00000559517.5:c.176A>T	ENSP00000453408.1:p.Asp59Val
ENST00000561070.5:c.176A>T	ENSP00000452850.1:p.Asp59Val
NM_001206897.1:c.401A>T	NP_001193826.1:p.Asp134Val
NM_003888.3:c.464A>T	NP_003879.2:p.Asp155Val
NM_170696.2:c.464A>T	NP_733797.1:p.Asp155Val
NM_170697.2:c.176A>T	NP_733798.1:p.Asp59Val
XM_024450095.1:c.464A>T	XP_024305863.1:p.Asp155Val
NM_003888.4:c.464A>T MANE Select	NP_003879.2:p.Asp155Val
NM_170696.3:c.464A>T	NP_733797.1:p.Asp155Val
NM_170697.3:c.176A>T	NP_733798.1:p.Asp59Val
NM_001206897.2:c.401A>T	NP_001193826.1:p.Asp134Val