Canonical Allele Identifier: CA2269944894

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486715G= , CM000679.2:g.63486715G=	GRCh38
NC_000017.10:g.61564076G= , CM000679.1:g.61564076G=	GRCh37
NC_000017.9:g.58917808G=	NCBI36
NG_011648.1:g.14643G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2217G= MANE Select	ENSP00000290866.4:p.Glu739=
ENST00000290863.10:c.495G=	ENSP00000290863.6:p.Glu165=
ENST00000290866.9:c.2217G=	ENSP00000290866.4:p.Glu739=
ENST00000413513.7:c.495G=	ENSP00000392247.3:p.Glu165=
ENST00000428043.5:c.2217G=	ENSP00000397593.2:p.Glu739=
ENST00000577647.2:c.495G=	ENSP00000464149.1:p.Glu165=
ENST00000578839.5:c.*287G=	ENSP00000462110.2:n.*287G=
ENST00000579204.1:c.398G=	ENSP00000464629.1:n.398G=
ENST00000579314.5:c.495G=	ENSP00000462599.1:p.Glu165=
ENST00000579726.5:c.779G=
ENST00000582005.5:c.*137G=	ENSP00000462002.1:n.*137G=
NM_000789.3:c.2217G=	NP_000780.1:p.Glu739=
NM_001178057.1:c.495G=	NP_001171528.1:p.Glu165=
NM_152830.2:c.495G=	NP_690043.1:p.Glu165=
XM_005257110.1:c.1668G=	XP_005257167.1:p.Glu556=
XM_006721737.2:c.555G=	XP_006721800.2:p.Glu185=
XM_006721737.3:c.555G=	XP_006721800.2:p.Glu185=
NM_000789.4:c.2217G= MANE Select	NP_000780.1:p.Glu739=
NM_001178057.2:c.495G=	NP_001171528.1:p.Glu165=
NM_152830.3:c.495G=	NP_690043.1:p.Glu165=
NM_001382700.1:c.1650G=	NP_001369629.1:p.Glu550=
NM_001382701.1:c.1365G=	NP_001369630.1:p.Glu455=
NM_001382702.1:c.147G=	NP_001369631.1:p.Glu49=
NR_168483.1:n.517G=