Canonical Allele Identifier: CA2180114124

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010717C= , CM000677.2:g.58010717C=	GRCh38
NC_000015.9:g.58302915C= , CM000677.1:g.58302915C=	GRCh37
NC_000015.8:g.56090207C=	NCBI36
NG_012259.1:g.59992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.425G= MANE Select	ENSP00000249750.4:p.Gly142=
ENST00000249750.8:c.425G=	ENSP00000249750.4:p.Gly142=
ENST00000347587.7:c.425G=	ENSP00000309623.3:p.Gly142=
ENST00000430119.6:c.*399G=	ENSP00000416754.2:n.*399G=
ENST00000537372.5:c.362G=	ENSP00000438296.1:p.Gly121=
ENST00000558231.5:c.338G=	ENSP00000453600.1:p.Gly113=
ENST00000559266.5:n.318+3141G=
ENST00000559517.5:c.137G=	ENSP00000453408.1:p.Gly46=
ENST00000561070.5:c.137G=	ENSP00000452850.1:p.Gly46=
NM_001206897.1:c.362G=	NP_001193826.1:p.Gly121=
NM_003888.3:c.425G=	NP_003879.2:p.Gly142=
NM_170696.2:c.425G=	NP_733797.1:p.Gly142=
NM_170697.2:c.137G=	NP_733798.1:p.Gly46=
XM_024450095.1:c.425G=	XP_024305863.1:p.Gly142=
NM_003888.4:c.425G= MANE Select	NP_003879.2:p.Gly142=
NM_170696.3:c.425G=	NP_733797.1:p.Gly142=
NM_170697.3:c.137G=	NP_733798.1:p.Gly46=
NM_001206897.2:c.362G=	NP_001193826.1:p.Gly121=