Canonical Allele Identifier: CA2269949985

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497171C= , CM000679.2:g.63497171C=	GRCh38
NC_000017.10:g.61574532C= , CM000679.1:g.61574532C=	GRCh37
NC_000017.9:g.58928264C=	NCBI36
NG_011648.1:g.25099C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3726C= MANE Select	ENSP00000290866.4:p.Arg1242=
ENST00000290863.10:c.2004C=	ENSP00000290863.6:p.Arg668=
ENST00000290866.9:c.3726C=	ENSP00000290866.4:p.Arg1242=
ENST00000413513.7:c.1881C=	ENSP00000392247.3:p.Arg627=
ENST00000428043.5:c.*148C=	ENSP00000397593.2:n.*148C=
ENST00000577647.2:c.1969+186C=	ENSP00000464149.1:n.1969+186C=
ENST00000578839.5:c.*1481C=	ENSP00000462110.2:n.*1481C=
ENST00000579314.5:c.*1455C=	ENSP00000462599.1:n.*1455C=
NM_000789.3:c.3726C=	NP_000780.1:p.Arg1242=
NM_001178057.1:c.1881C=	NP_001171528.1:p.Arg627=
NM_152830.2:c.2004C=	NP_690043.1:p.Arg668=
XM_005257110.1:c.3177C=	XP_005257167.1:p.Arg1059=
XM_006721737.2:c.2064C=	XP_006721800.2:p.Arg688=
XM_006721737.3:c.2064C=	XP_006721800.2:p.Arg688=
NM_000789.4:c.3726C= MANE Select	NP_000780.1:p.Arg1242=
NM_001178057.2:c.1881C=	NP_001171528.1:p.Arg627=
NM_152830.3:c.2004C=	NP_690043.1:p.Arg668=
NM_001382700.1:c.3159C=	NP_001369629.1:p.Arg1053=
NM_001382701.1:c.2874C=	NP_001369630.1:p.Arg958=
NM_001382702.1:c.1341C=	NP_001369631.1:p.Arg447=
NR_168483.1:n.2104C=