Canonical Allele Identifier: CA2180114057

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010677A= , CM000677.2:g.58010677A=	GRCh38
NC_000015.9:g.58302875A= , CM000677.1:g.58302875A=	GRCh37
NC_000015.8:g.56090167A=	NCBI36
NG_012259.1:g.60032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.465T= MANE Select	ENSP00000249750.4:p.Asp155=
ENST00000249750.8:c.465T=	ENSP00000249750.4:p.Asp155=
ENST00000347587.7:c.465T=	ENSP00000309623.3:p.Asp155=
ENST00000430119.6:c.*439T=	ENSP00000416754.2:n.*439T=
ENST00000537372.5:c.402T=	ENSP00000438296.1:p.Asp134=
ENST00000558231.5:c.378T=	ENSP00000453600.1:p.Asp126=
ENST00000559266.5:n.318+3181T=
ENST00000559517.5:c.177T=	ENSP00000453408.1:p.Asp59=
ENST00000561070.5:c.177T=	ENSP00000452850.1:p.Asp59=
NM_001206897.1:c.402T=	NP_001193826.1:p.Asp134=
NM_003888.3:c.465T=	NP_003879.2:p.Asp155=
NM_170696.2:c.465T=	NP_733797.1:p.Asp155=
NM_170697.2:c.177T=	NP_733798.1:p.Asp59=
XM_024450095.1:c.465T=	XP_024305863.1:p.Asp155=
NM_003888.4:c.465T= MANE Select	NP_003879.2:p.Asp155=
NM_170696.3:c.465T=	NP_733797.1:p.Asp155=
NM_170697.3:c.177T=	NP_733798.1:p.Asp59=
NM_001206897.2:c.402T=	NP_001193826.1:p.Asp134=