Canonical Allele Identifier: CA2269949753

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496802G= , CM000679.2:g.63496802G=	GRCh38
NC_000017.10:g.61574163G= , CM000679.1:g.61574163G=	GRCh37
NC_000017.9:g.58927895G=	NCBI36
NG_011648.1:g.24730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3508G= MANE Select	ENSP00000290866.4:p.Ala1170=
ENST00000290863.10:c.1786G=	ENSP00000290863.6:p.Ala596=
ENST00000290866.9:c.3508G=	ENSP00000290866.4:p.Ala1170=
ENST00000413513.7:c.1663G=	ENSP00000392247.3:p.Ala555=
ENST00000428043.5:c.3508G=	ENSP00000397593.2:p.Ala1170=
ENST00000577418.5:n.518G=
ENST00000577647.2:c.1786G=	ENSP00000464149.1:p.Ala596=
ENST00000578839.5:c.*1263G=	ENSP00000462110.2:n.*1263G=
ENST00000579314.5:c.*1237G=	ENSP00000462599.1:n.*1237G=
ENST00000579409.1:c.195G=
ENST00000582244.1:n.382G=
NM_000789.3:c.3508G=	NP_000780.1:p.Ala1170=
NM_001178057.1:c.1663G=	NP_001171528.1:p.Ala555=
NM_152830.2:c.1786G=	NP_690043.1:p.Ala596=
XM_005257110.1:c.2959G=	XP_005257167.1:p.Ala987=
XM_006721737.2:c.1846G=	XP_006721800.2:p.Ala616=
XM_006721737.3:c.1846G=	XP_006721800.2:p.Ala616=
NM_000789.4:c.3508G= MANE Select	NP_000780.1:p.Ala1170=
NM_001178057.2:c.1663G=	NP_001171528.1:p.Ala555=
NM_152830.3:c.1786G=	NP_690043.1:p.Ala596=
NM_001382700.1:c.2941G=	NP_001369629.1:p.Ala981=
NM_001382701.1:c.2656G=	NP_001369630.1:p.Ala886=
NM_001382702.1:c.1123G=	NP_001369631.1:p.Ala375=
NR_168483.1:n.1886G=