Canonical Allele Identifier: CA392790036

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302889C>G (hg19) ; chr15:g.58010691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010691C>G , CM000677.2:g.58010691C>G	GRCh38
NC_000015.9:g.58302889C>G , CM000677.1:g.58302889C>G	GRCh37
NC_000015.8:g.56090181C>G	NCBI36
NG_012259.1:g.60018G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.451G>C MANE Select	ENSP00000249750.4:p.Ala151Pro
ENST00000249750.8:c.451G>C	ENSP00000249750.4:p.Ala151Pro
ENST00000347587.7:c.451G>C	ENSP00000309623.3:p.Ala151Pro
ENST00000430119.6:c.*425G>C	ENSP00000416754.2:n.*425G>C
ENST00000537372.5:c.388G>C	ENSP00000438296.1:p.Ala130Pro
ENST00000558231.5:c.364G>C	ENSP00000453600.1:p.Ala122Pro
ENST00000559266.5:n.318+3167G>C
ENST00000559517.5:c.163G>C	ENSP00000453408.1:p.Ala55Pro
ENST00000561070.5:c.163G>C	ENSP00000452850.1:p.Ala55Pro
NM_001206897.1:c.388G>C	NP_001193826.1:p.Ala130Pro
NM_003888.3:c.451G>C	NP_003879.2:p.Ala151Pro
NM_170696.2:c.451G>C	NP_733797.1:p.Ala151Pro
NM_170697.2:c.163G>C	NP_733798.1:p.Ala55Pro
XM_024450095.1:c.451G>C	XP_024305863.1:p.Ala151Pro
NM_003888.4:c.451G>C MANE Select	NP_003879.2:p.Ala151Pro
NM_170696.3:c.451G>C	NP_733797.1:p.Ala151Pro
NM_170697.3:c.163G>C	NP_733798.1:p.Ala55Pro
NM_001206897.2:c.388G>C	NP_001193826.1:p.Ala130Pro