Canonical Allele Identifier: CA2180114122

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010716G= , CM000677.2:g.58010716G=	GRCh38
NC_000015.9:g.58302914G= , CM000677.1:g.58302914G=	GRCh37
NC_000015.8:g.56090206G=	NCBI36
NG_012259.1:g.59993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.426C= MANE Select	ENSP00000249750.4:p.Gly142=
ENST00000249750.8:c.426C=	ENSP00000249750.4:p.Gly142=
ENST00000347587.7:c.426C=	ENSP00000309623.3:p.Gly142=
ENST00000430119.6:c.*400C=	ENSP00000416754.2:n.*400C=
ENST00000537372.5:c.363C=	ENSP00000438296.1:p.Gly121=
ENST00000558231.5:c.339C=	ENSP00000453600.1:p.Gly113=
ENST00000559266.5:n.318+3142C=
ENST00000559517.5:c.138C=	ENSP00000453408.1:p.Gly46=
ENST00000561070.5:c.138C=	ENSP00000452850.1:p.Gly46=
NM_001206897.1:c.363C=	NP_001193826.1:p.Gly121=
NM_003888.3:c.426C=	NP_003879.2:p.Gly142=
NM_170696.2:c.426C=	NP_733797.1:p.Gly142=
NM_170697.2:c.138C=	NP_733798.1:p.Gly46=
XM_024450095.1:c.426C=	XP_024305863.1:p.Gly142=
NM_003888.4:c.426C= MANE Select	NP_003879.2:p.Gly142=
NM_170696.3:c.426C=	NP_733797.1:p.Gly142=
NM_170697.3:c.138C=	NP_733798.1:p.Gly46=
NM_001206897.2:c.363C=	NP_001193826.1:p.Gly121=