Canonical Allele Identifier: CA392790153

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302912A>T (hg19) ; chr15:g.58010714A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010714A>T , CM000677.2:g.58010714A>T	GRCh38
NC_000015.9:g.58302912A>T , CM000677.1:g.58302912A>T	GRCh37
NC_000015.8:g.56090204A>T	NCBI36
NG_012259.1:g.59995T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.428T>A MANE Select	ENSP00000249750.4:p.Val143Asp
ENST00000249750.8:c.428T>A	ENSP00000249750.4:p.Val143Asp
ENST00000347587.7:c.428T>A	ENSP00000309623.3:p.Val143Asp
ENST00000430119.6:c.*402T>A	ENSP00000416754.2:n.*402T>A
ENST00000537372.5:c.365T>A	ENSP00000438296.1:p.Val122Asp
ENST00000558231.5:c.341T>A	ENSP00000453600.1:p.Val114Asp
ENST00000559266.5:n.318+3144T>A
ENST00000559517.5:c.140T>A	ENSP00000453408.1:p.Val47Asp
ENST00000561070.5:c.140T>A	ENSP00000452850.1:p.Val47Asp
NM_001206897.1:c.365T>A	NP_001193826.1:p.Val122Asp
NM_003888.3:c.428T>A	NP_003879.2:p.Val143Asp
NM_170696.2:c.428T>A	NP_733797.1:p.Val143Asp
NM_170697.2:c.140T>A	NP_733798.1:p.Val47Asp
XM_024450095.1:c.428T>A	XP_024305863.1:p.Val143Asp
NM_003888.4:c.428T>A MANE Select	NP_003879.2:p.Val143Asp
NM_170696.3:c.428T>A	NP_733797.1:p.Val143Asp
NM_170697.3:c.140T>A	NP_733798.1:p.Val47Asp
NM_001206897.2:c.365T>A	NP_001193826.1:p.Val122Asp