Canonical Allele Identifier: CA2180114051

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010665C= , CM000677.2:g.58010665C=	GRCh38
NC_000015.9:g.58302863C= , CM000677.1:g.58302863C=	GRCh37
NC_000015.8:g.56090155C=	NCBI36
NG_012259.1:g.60044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.477G= MANE Select	ENSP00000249750.4:p.Gly159=
ENST00000249750.8:c.477G=	ENSP00000249750.4:p.Gly159=
ENST00000347587.7:c.477G=	ENSP00000309623.3:p.Gly159=
ENST00000430119.6:c.*451G=	ENSP00000416754.2:n.*451G=
ENST00000537372.5:c.414G=	ENSP00000438296.1:p.Gly138=
ENST00000558231.5:c.390G=	ENSP00000453600.1:p.Gly130=
ENST00000559266.5:n.318+3193G=
ENST00000559517.5:c.189G=	ENSP00000453408.1:p.Gly63=
ENST00000561070.5:c.189G=	ENSP00000452850.1:p.Gly63=
NM_001206897.1:c.414G=	NP_001193826.1:p.Gly138=
NM_003888.3:c.477G=	NP_003879.2:p.Gly159=
NM_170696.2:c.477G=	NP_733797.1:p.Gly159=
NM_170697.2:c.189G=	NP_733798.1:p.Gly63=
XM_024450095.1:c.477G=	XP_024305863.1:p.Gly159=
NM_003888.4:c.477G= MANE Select	NP_003879.2:p.Gly159=
NM_170696.3:c.477G=	NP_733797.1:p.Gly159=
NM_170697.3:c.189G=	NP_733798.1:p.Gly63=
NM_001206897.2:c.414G=	NP_001193826.1:p.Gly138=