Canonical Allele Identifier: CA2180114062

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010682C= , CM000677.2:g.58010682C=	GRCh38
NC_000015.9:g.58302880C= , CM000677.1:g.58302880C=	GRCh37
NC_000015.8:g.56090172C=	NCBI36
NG_012259.1:g.60027G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.460G= MANE Select	ENSP00000249750.4:p.Ala154=
ENST00000249750.8:c.460G=	ENSP00000249750.4:p.Ala154=
ENST00000347587.7:c.460G=	ENSP00000309623.3:p.Ala154=
ENST00000430119.6:c.*434G=	ENSP00000416754.2:n.*434G=
ENST00000537372.5:c.397G=	ENSP00000438296.1:p.Ala133=
ENST00000558231.5:c.373G=	ENSP00000453600.1:p.Ala125=
ENST00000559266.5:n.318+3176G=
ENST00000559517.5:c.172G=	ENSP00000453408.1:p.Ala58=
ENST00000561070.5:c.172G=	ENSP00000452850.1:p.Ala58=
NM_001206897.1:c.397G=	NP_001193826.1:p.Ala133=
NM_003888.3:c.460G=	NP_003879.2:p.Ala154=
NM_170696.2:c.460G=	NP_733797.1:p.Ala154=
NM_170697.2:c.172G=	NP_733798.1:p.Ala58=
XM_024450095.1:c.460G=	XP_024305863.1:p.Ala154=
NM_003888.4:c.460G= MANE Select	NP_003879.2:p.Ala154=
NM_170696.3:c.460G=	NP_733797.1:p.Ala154=
NM_170697.3:c.172G=	NP_733798.1:p.Ala58=
NM_001206897.2:c.397G=	NP_001193826.1:p.Ala133=