Canonical Allele Identifier: CA2269944852

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486620G= , CM000679.2:g.63486620G=	GRCh38
NC_000017.10:g.61563981G= , CM000679.1:g.61563981G=	GRCh37
NC_000017.9:g.58917713G=	NCBI36
NG_011648.1:g.14548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2122G= MANE Select	ENSP00000290866.4:p.Asp708=
ENST00000290863.10:c.400G=	ENSP00000290863.6:p.Asp134=
ENST00000290866.9:c.2122G=	ENSP00000290866.4:p.Asp708=
ENST00000413513.7:c.400G=	ENSP00000392247.3:p.Asp134=
ENST00000428043.5:c.2122G=	ENSP00000397593.2:p.Asp708=
ENST00000577647.2:c.400G=	ENSP00000464149.1:p.Asp134=
ENST00000578839.5:c.*192G=	ENSP00000462110.2:n.*192G=
ENST00000579204.1:c.303G=	ENSP00000464629.1:n.303G=
ENST00000579314.5:c.400G=	ENSP00000462599.1:p.Asp134=
ENST00000579726.5:c.684G=
ENST00000582005.5:c.*42G=	ENSP00000462002.1:n.*42G=
NM_000789.3:c.2122G=	NP_000780.1:p.Asp708=
NM_001178057.1:c.400G=	NP_001171528.1:p.Asp134=
NM_152830.2:c.400G=	NP_690043.1:p.Asp134=
XM_005257110.1:c.1573G=	XP_005257167.1:p.Asp525=
XM_006721737.2:c.460G=	XP_006721800.2:p.Asp154=
XM_006721737.3:c.460G=	XP_006721800.2:p.Asp154=
NM_000789.4:c.2122G= MANE Select	NP_000780.1:p.Asp708=
NM_001178057.2:c.400G=	NP_001171528.1:p.Asp134=
NM_152830.3:c.400G=	NP_690043.1:p.Asp134=
NM_001382700.1:c.1555G=	NP_001369629.1:p.Asp519=
NM_001382701.1:c.1270G=	NP_001369630.1:p.Asp424=
NM_001382702.1:c.52G=	NP_001369631.1:p.Asp18=
NR_168483.1:n.422G=