Canonical Allele Identifier: CA2180114055

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58010671A= , CM000677.2:g.58010671A=	GRCh38
NC_000015.9:g.58302869A= , CM000677.1:g.58302869A=	GRCh37
NC_000015.8:g.56090161A=	NCBI36
NG_012259.1:g.60038T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.471T= MANE Select	ENSP00000249750.4:p.Ile157=
ENST00000249750.8:c.471T=	ENSP00000249750.4:p.Ile157=
ENST00000347587.7:c.471T=	ENSP00000309623.3:p.Ile157=
ENST00000430119.6:c.*445T=	ENSP00000416754.2:n.*445T=
ENST00000537372.5:c.408T=	ENSP00000438296.1:p.Ile136=
ENST00000558231.5:c.384T=	ENSP00000453600.1:p.Ile128=
ENST00000559266.5:n.318+3187T=
ENST00000559517.5:c.183T=	ENSP00000453408.1:p.Ile61=
ENST00000561070.5:c.183T=	ENSP00000452850.1:p.Ile61=
NM_001206897.1:c.408T=	NP_001193826.1:p.Ile136=
NM_003888.3:c.471T=	NP_003879.2:p.Ile157=
NM_170696.2:c.471T=	NP_733797.1:p.Ile157=
NM_170697.2:c.183T=	NP_733798.1:p.Ile61=
XM_024450095.1:c.471T=	XP_024305863.1:p.Ile157=
NM_003888.4:c.471T= MANE Select	NP_003879.2:p.Ile157=
NM_170696.3:c.471T=	NP_733797.1:p.Ile157=
NM_170697.3:c.183T=	NP_733798.1:p.Ile61=
NM_001206897.2:c.408T=	NP_001193826.1:p.Ile136=