Canonical Allele Identifier: CA392790296

Gene: ALDH1A2

Linked Data

• MyVariant Identifiers: chr15:g.58302976T>A (hg19) ; chr15:g.58010778T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010778T>A , CM000677.2:g.58010778T>A	GRCh38
NC_000015.9:g.58302976T>A , CM000677.1:g.58302976T>A	GRCh37
NC_000015.8:g.56090268T>A	NCBI36
NG_012259.1:g.59931A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.364A>T MANE Select	ENSP00000249750.4:p.Thr122Ser
ENST00000249750.8:c.364A>T	ENSP00000249750.4:p.Thr122Ser
ENST00000347587.7:c.364A>T	ENSP00000309623.3:p.Thr122Ser
ENST00000430119.6:c.*338A>T	ENSP00000416754.2:n.*338A>T
ENST00000537372.5:c.301A>T	ENSP00000438296.1:p.Thr101Ser
ENST00000558231.5:c.277A>T	ENSP00000453600.1:p.Thr93Ser
ENST00000559266.5:n.318+3080A>T
ENST00000559517.5:c.76A>T	ENSP00000453408.1:p.Thr26Ser
ENST00000561070.5:c.76A>T	ENSP00000452850.1:p.Thr26Ser
NM_001206897.1:c.301A>T	NP_001193826.1:p.Thr101Ser
NM_003888.3:c.364A>T	NP_003879.2:p.Thr122Ser
NM_170696.2:c.364A>T	NP_733797.1:p.Thr122Ser
NM_170697.2:c.76A>T	NP_733798.1:p.Thr26Ser
XM_024450095.1:c.364A>T	XP_024305863.1:p.Thr122Ser
NM_003888.4:c.364A>T MANE Select	NP_003879.2:p.Thr122Ser
NM_170696.3:c.364A>T	NP_733797.1:p.Thr122Ser
NM_170697.3:c.76A>T	NP_733798.1:p.Thr26Ser
NM_001206897.2:c.301A>T	NP_001193826.1:p.Thr101Ser