Canonical Allele Identifier: CA2269949969

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497140G= , CM000679.2:g.63497140G=	GRCh38
NC_000017.10:g.61574501G= , CM000679.1:g.61574501G=	GRCh37
NC_000017.9:g.58928233G=	NCBI36
NG_011648.1:g.25068G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3695G= MANE Select	ENSP00000290866.4:p.Arg1232=
ENST00000290863.10:c.1973G=	ENSP00000290863.6:p.Arg658=
ENST00000290866.9:c.3695G=	ENSP00000290866.4:p.Arg1232=
ENST00000413513.7:c.1850G=	ENSP00000392247.3:p.Arg617=
ENST00000428043.5:c.*117G=	ENSP00000397593.2:n.*117G=
ENST00000577418.5:n.705G=
ENST00000577647.2:c.1969+155G=	ENSP00000464149.1:n.1969+155G=
ENST00000578839.5:c.*1450G=	ENSP00000462110.2:n.*1450G=
ENST00000579314.5:c.*1424G=	ENSP00000462599.1:n.*1424G=
ENST00000579409.1:c.533G=
NM_000789.3:c.3695G=	NP_000780.1:p.Arg1232=
NM_001178057.1:c.1850G=	NP_001171528.1:p.Arg617=
NM_152830.2:c.1973G=	NP_690043.1:p.Arg658=
XM_005257110.1:c.3146G=	XP_005257167.1:p.Arg1049=
XM_006721737.2:c.2033G=	XP_006721800.2:p.Arg678=
XM_006721737.3:c.2033G=	XP_006721800.2:p.Arg678=
NM_000789.4:c.3695G= MANE Select	NP_000780.1:p.Arg1232=
NM_001178057.2:c.1850G=	NP_001171528.1:p.Arg617=
NM_152830.3:c.1973G=	NP_690043.1:p.Arg658=
NM_001382700.1:c.3128G=	NP_001369629.1:p.Arg1043=
NM_001382701.1:c.2843G=	NP_001369630.1:p.Arg948=
NM_001382702.1:c.1310G=	NP_001369631.1:p.Arg437=
NR_168483.1:n.2073G=