Canonical Allele Identifier: CA2269950002

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497211C= , CM000679.2:g.63497211C=	GRCh38
NC_000017.10:g.61574572C= , CM000679.1:g.61574572C=	GRCh37
NC_000017.9:g.58928304C=	NCBI36
NG_011648.1:g.25139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3766C= MANE Select	ENSP00000290866.4:p.Arg1256=
ENST00000290863.10:c.2044C=	ENSP00000290863.6:p.Arg682=
ENST00000290866.9:c.3766C=	ENSP00000290866.4:p.Arg1256=
ENST00000413513.7:c.1921C=	ENSP00000392247.3:p.Arg641=
ENST00000428043.5:c.*188C=	ENSP00000397593.2:n.*188C=
ENST00000577647.2:c.1969+226C=	ENSP00000464149.1:n.1969+226C=
ENST00000578839.5:c.*1521C=	ENSP00000462110.2:n.*1521C=
ENST00000579314.5:c.*1495C=	ENSP00000462599.1:n.*1495C=
NM_000789.3:c.3766C=	NP_000780.1:p.Arg1256=
NM_001178057.1:c.1921C=	NP_001171528.1:p.Arg641=
NM_152830.2:c.2044C=	NP_690043.1:p.Arg682=
XM_005257110.1:c.3217C=	XP_005257167.1:p.Arg1073=
XM_006721737.2:c.2104C=	XP_006721800.2:p.Arg702=
XM_006721737.3:c.2104C=	XP_006721800.2:p.Arg702=
NM_000789.4:c.3766C= MANE Select	NP_000780.1:p.Arg1256=
NM_001178057.2:c.1921C=	NP_001171528.1:p.Arg641=
NM_152830.3:c.2044C=	NP_690043.1:p.Arg682=
NM_001382700.1:c.3199C=	NP_001369629.1:p.Arg1067=
NM_001382701.1:c.2914C=	NP_001369630.1:p.Arg972=
NM_001382702.1:c.1381C=	NP_001369631.1:p.Arg461=
NR_168483.1:n.2144C=