Canonical Allele Identifier: CA2269949990

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497181C= , CM000679.2:g.63497181C=	GRCh38
NC_000017.10:g.61574542C= , CM000679.1:g.61574542C=	GRCh37
NC_000017.9:g.58928274C=	NCBI36
NG_011648.1:g.25109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3736C= MANE Select	ENSP00000290866.4:p.Leu1246=
ENST00000290863.10:c.2014C=	ENSP00000290863.6:p.Leu672=
ENST00000290866.9:c.3736C=	ENSP00000290866.4:p.Leu1246=
ENST00000413513.7:c.1891C=	ENSP00000392247.3:p.Leu631=
ENST00000428043.5:c.*158C=	ENSP00000397593.2:n.*158C=
ENST00000577647.2:c.1969+196C=	ENSP00000464149.1:n.1969+196C=
ENST00000578839.5:c.*1491C=	ENSP00000462110.2:n.*1491C=
ENST00000579314.5:c.*1465C=	ENSP00000462599.1:n.*1465C=
NM_000789.3:c.3736C=	NP_000780.1:p.Leu1246=
NM_001178057.1:c.1891C=	NP_001171528.1:p.Leu631=
NM_152830.2:c.2014C=	NP_690043.1:p.Leu672=
XM_005257110.1:c.3187C=	XP_005257167.1:p.Leu1063=
XM_006721737.2:c.2074C=	XP_006721800.2:p.Leu692=
XM_006721737.3:c.2074C=	XP_006721800.2:p.Leu692=
NM_000789.4:c.3736C= MANE Select	NP_000780.1:p.Leu1246=
NM_001178057.2:c.1891C=	NP_001171528.1:p.Leu631=
NM_152830.3:c.2014C=	NP_690043.1:p.Leu672=
NM_001382700.1:c.3169C=	NP_001369629.1:p.Leu1057=
NM_001382701.1:c.2884C=	NP_001369630.1:p.Leu962=
NM_001382702.1:c.1351C=	NP_001369631.1:p.Leu451=
NR_168483.1:n.2114C=