Canonical Allele Identifier: CA2269949971

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497143C= , CM000679.2:g.63497143C=	GRCh38
NC_000017.10:g.61574504C= , CM000679.1:g.61574504C=	GRCh37
NC_000017.9:g.58928236C=	NCBI36
NG_011648.1:g.25071C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3698C= MANE Select	ENSP00000290866.4:p.Ser1233=
ENST00000290863.10:c.1976C=	ENSP00000290863.6:p.Ser659=
ENST00000290866.9:c.3698C=	ENSP00000290866.4:p.Ser1233=
ENST00000413513.7:c.1853C=	ENSP00000392247.3:p.Ser618=
ENST00000428043.5:c.*120C=	ENSP00000397593.2:n.*120C=
ENST00000577418.5:n.708C=
ENST00000577647.2:c.1969+158C=	ENSP00000464149.1:n.1969+158C=
ENST00000578839.5:c.*1453C=	ENSP00000462110.2:n.*1453C=
ENST00000579314.5:c.*1427C=	ENSP00000462599.1:n.*1427C=
ENST00000579409.1:c.536C=
NM_000789.3:c.3698C=	NP_000780.1:p.Ser1233=
NM_001178057.1:c.1853C=	NP_001171528.1:p.Ser618=
NM_152830.2:c.1976C=	NP_690043.1:p.Ser659=
XM_005257110.1:c.3149C=	XP_005257167.1:p.Ser1050=
XM_006721737.2:c.2036C=	XP_006721800.2:p.Ser679=
XM_006721737.3:c.2036C=	XP_006721800.2:p.Ser679=
NM_000789.4:c.3698C= MANE Select	NP_000780.1:p.Ser1233=
NM_001178057.2:c.1853C=	NP_001171528.1:p.Ser618=
NM_152830.3:c.1976C=	NP_690043.1:p.Ser659=
NM_001382700.1:c.3131C=	NP_001369629.1:p.Ser1044=
NM_001382701.1:c.2846C=	NP_001369630.1:p.Ser949=
NM_001382702.1:c.1313C=	NP_001369631.1:p.Ser438=
NR_168483.1:n.2076C=