Canonical Allele Identifier: CA2269944846

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486609C= , CM000679.2:g.63486609C=	GRCh38
NC_000017.10:g.61563970C= , CM000679.1:g.61563970C=	GRCh37
NC_000017.9:g.58917702C=	NCBI36
NG_011648.1:g.14537C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2111C= MANE Select	ENSP00000290866.4:p.Ala704=
ENST00000290863.10:c.389C=	ENSP00000290863.6:p.Ala130=
ENST00000290866.9:c.2111C=	ENSP00000290866.4:p.Ala704=
ENST00000413513.7:c.389C=	ENSP00000392247.3:p.Ala130=
ENST00000428043.5:c.2111C=	ENSP00000397593.2:p.Ala704=
ENST00000577647.2:c.389C=	ENSP00000464149.1:p.Ala130=
ENST00000578839.5:c.*181C=	ENSP00000462110.2:n.*181C=
ENST00000579204.1:c.292C=	ENSP00000464629.1:n.292C=
ENST00000579314.5:c.389C=	ENSP00000462599.1:p.Ala130=
ENST00000579726.5:c.673C=
ENST00000582005.5:c.*31C=	ENSP00000462002.1:n.*31C=
NM_000789.3:c.2111C=	NP_000780.1:p.Ala704=
NM_001178057.1:c.389C=	NP_001171528.1:p.Ala130=
NM_152830.2:c.389C=	NP_690043.1:p.Ala130=
XM_005257110.1:c.1562C=	XP_005257167.1:p.Ala521=
XM_006721737.2:c.449C=	XP_006721800.2:p.Ala150=
XM_006721737.3:c.449C=	XP_006721800.2:p.Ala150=
NM_000789.4:c.2111C= MANE Select	NP_000780.1:p.Ala704=
NM_001178057.2:c.389C=	NP_001171528.1:p.Ala130=
NM_152830.3:c.389C=	NP_690043.1:p.Ala130=
NM_001382700.1:c.1544C=	NP_001369629.1:p.Ala515=
NM_001382701.1:c.1259C=	NP_001369630.1:p.Ala420=
NM_001382702.1:c.41C=	NP_001369631.1:p.Ala14=
NR_168483.1:n.411C=