Canonical Allele Identifier: CA392790152

Gene: ALDH1A2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.428T>C MANE Select	ENSP00000249750.4:p.Val143Ala
ENST00000249750.8:c.428T>C	ENSP00000249750.4:p.Val143Ala
ENST00000347587.7:c.428T>C	ENSP00000309623.3:p.Val143Ala
ENST00000430119.6:c.*402T>C	ENSP00000416754.2:n.*402T>C
ENST00000537372.5:c.365T>C	ENSP00000438296.1:p.Val122Ala
ENST00000558231.5:c.341T>C	ENSP00000453600.1:p.Val114Ala
ENST00000559266.5:n.318+3144T>C
ENST00000559517.5:c.140T>C	ENSP00000453408.1:p.Val47Ala
ENST00000561070.5:c.140T>C	ENSP00000452850.1:p.Val47Ala
NM_001206897.1:c.365T>C	NP_001193826.1:p.Val122Ala
NM_003888.3:c.428T>C	NP_003879.2:p.Val143Ala
NM_170696.2:c.428T>C	NP_733797.1:p.Val143Ala
NM_170697.2:c.140T>C	NP_733798.1:p.Val47Ala
XM_024450095.1:c.428T>C	XP_024305863.1:p.Val143Ala
NM_003888.4:c.428T>C MANE Select	NP_003879.2:p.Val143Ala
NM_170696.3:c.428T>C	NP_733797.1:p.Val143Ala
NM_170697.3:c.140T>C	NP_733798.1:p.Val47Ala
NM_001206897.2:c.365T>C	NP_001193826.1:p.Val122Ala