Canonical Allele Identifier: CA2269949967

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497137C= , CM000679.2:g.63497137C=	GRCh38
NC_000017.10:g.61574498C= , CM000679.1:g.61574498C=	GRCh37
NC_000017.9:g.58928230C=	NCBI36
NG_011648.1:g.25065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3692C= MANE Select	ENSP00000290866.4:p.Ala1231=
ENST00000290863.10:c.1970C=	ENSP00000290863.6:p.Ala657=
ENST00000290866.9:c.3692C=	ENSP00000290866.4:p.Ala1231=
ENST00000413513.7:c.1847C=	ENSP00000392247.3:p.Ala616=
ENST00000428043.5:c.*114C=	ENSP00000397593.2:n.*114C=
ENST00000577418.5:n.702C=
ENST00000577647.2:c.1969+152C=	ENSP00000464149.1:n.1969+152C=
ENST00000578839.5:c.*1447C=	ENSP00000462110.2:n.*1447C=
ENST00000579314.5:c.*1421C=	ENSP00000462599.1:n.*1421C=
ENST00000579409.1:c.530C=
NM_000789.3:c.3692C=	NP_000780.1:p.Ala1231=
NM_001178057.1:c.1847C=	NP_001171528.1:p.Ala616=
NM_152830.2:c.1970C=	NP_690043.1:p.Ala657=
XM_005257110.1:c.3143C=	XP_005257167.1:p.Ala1048=
XM_006721737.2:c.2030C=	XP_006721800.2:p.Ala677=
XM_006721737.3:c.2030C=	XP_006721800.2:p.Ala677=
NM_000789.4:c.3692C= MANE Select	NP_000780.1:p.Ala1231=
NM_001178057.2:c.1847C=	NP_001171528.1:p.Ala616=
NM_152830.3:c.1970C=	NP_690043.1:p.Ala657=
NM_001382700.1:c.3125C=	NP_001369629.1:p.Ala1042=
NM_001382701.1:c.2840C=	NP_001369630.1:p.Ala947=
NM_001382702.1:c.1307C=	NP_001369631.1:p.Ala436=
NR_168483.1:n.2070C=