Canonical Allele Identifier: CA2269949823

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496943G= , CM000679.2:g.63496943G=	GRCh38
NC_000017.10:g.61574304G= , CM000679.1:g.61574304G=	GRCh37
NC_000017.9:g.58928036G=	NCBI36
NG_011648.1:g.24871G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3649G= MANE Select	ENSP00000290866.4:p.Glu1217=
ENST00000290863.10:c.1927G=	ENSP00000290863.6:p.Glu643=
ENST00000290866.9:c.3649G=	ENSP00000290866.4:p.Glu1217=
ENST00000413513.7:c.1804G=	ENSP00000392247.3:p.Glu602=
ENST00000428043.5:c.3649G=	ENSP00000397593.2:p.Glu1217=
ENST00000577418.5:n.659G=
ENST00000577647.2:c.1927G=	ENSP00000464149.1:p.Glu643=
ENST00000578839.5:c.*1404G=	ENSP00000462110.2:n.*1404G=
ENST00000579314.5:c.*1378G=	ENSP00000462599.1:n.*1378G=
ENST00000579409.1:c.336G=
ENST00000582244.1:n.523G=
NM_000789.3:c.3649G=	NP_000780.1:p.Glu1217=
NM_001178057.1:c.1804G=	NP_001171528.1:p.Glu602=
NM_152830.2:c.1927G=	NP_690043.1:p.Glu643=
XM_005257110.1:c.3100G=	XP_005257167.1:p.Glu1034=
XM_006721737.2:c.1987G=	XP_006721800.2:p.Glu663=
XM_006721737.3:c.1987G=	XP_006721800.2:p.Glu663=
NM_000789.4:c.3649G= MANE Select	NP_000780.1:p.Glu1217=
NM_001178057.2:c.1804G=	NP_001171528.1:p.Glu602=
NM_152830.3:c.1927G=	NP_690043.1:p.Glu643=
NM_001382700.1:c.3082G=	NP_001369629.1:p.Glu1028=
NM_001382701.1:c.2797G=	NP_001369630.1:p.Glu933=
NM_001382702.1:c.1264G=	NP_001369631.1:p.Glu422=
NR_168483.1:n.2027G=