Canonical Allele Identifier: CA2269950064

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497325G= , CM000679.2:g.63497325G=	GRCh38
NC_000017.10:g.61574686G= , CM000679.1:g.61574686G=	GRCh37
NC_000017.9:g.58928418G=	NCBI36
NG_011648.1:g.25253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3880G= MANE Select	ENSP00000290866.4:p.Gly1294=
ENST00000290863.10:c.2158G=	ENSP00000290863.6:p.Gly720=
ENST00000290866.9:c.3880G=	ENSP00000290866.4:p.Gly1294=
ENST00000413513.7:c.2035G=	ENSP00000392247.3:p.Gly679=
ENST00000428043.5:c.*302G=	ENSP00000397593.2:n.*302G=
ENST00000577647.2:c.1969+340G=	ENSP00000464149.1:n.1969+340G=
ENST00000578839.5:c.*1635G=	ENSP00000462110.2:n.*1635G=
ENST00000579314.5:c.*1609G=	ENSP00000462599.1:n.*1609G=
NM_000789.3:c.3880G=	NP_000780.1:p.Gly1294=
NM_001178057.1:c.2035G=	NP_001171528.1:p.Gly679=
NM_152830.2:c.2158G=	NP_690043.1:p.Gly720=
XM_005257110.1:c.3331G=	XP_005257167.1:p.Gly1111=
XM_006721737.2:c.2218G=	XP_006721800.2:p.Gly740=
XM_006721737.3:c.2218G=	XP_006721800.2:p.Gly740=
NM_000789.4:c.3880G= MANE Select	NP_000780.1:p.Gly1294=
NM_001178057.2:c.2035G=	NP_001171528.1:p.Gly679=
NM_152830.3:c.2158G=	NP_690043.1:p.Gly720=
NM_001382700.1:c.3313G=	NP_001369629.1:p.Gly1105=
NM_001382701.1:c.3028G=	NP_001369630.1:p.Gly1010=
NM_001382702.1:c.1495G=	NP_001369631.1:p.Gly499=
NR_168483.1:n.2258G=