Canonical Allele Identifier: CA2269945953

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488704G= , CM000679.2:g.63488704G=	GRCh38
NC_000017.10:g.61566065G= , CM000679.1:g.61566065G=	GRCh37
NC_000017.9:g.58919797G=	NCBI36
NG_011648.1:g.16632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2362G= MANE Select	ENSP00000290866.4:p.Glu788=
ENST00000290863.10:c.640G=	ENSP00000290863.6:p.Glu214=
ENST00000290866.9:c.2362G=	ENSP00000290866.4:p.Glu788=
ENST00000413513.7:c.640G=	ENSP00000392247.3:p.Glu214=
ENST00000428043.5:c.2362G=	ENSP00000397593.2:p.Glu788=
ENST00000577647.2:c.640G=	ENSP00000464149.1:p.Glu214=
ENST00000578839.5:c.*432G=	ENSP00000462110.2:n.*432G=
ENST00000579204.1:c.621G=	ENSP00000464629.1:n.621G=
ENST00000579314.5:c.*91G=	ENSP00000462599.1:n.*91G=
ENST00000582005.5:c.*282G=	ENSP00000462002.1:n.*282G=
ENST00000582761.1:c.130G=	ENSP00000462909.1:p.Glu44=
ENST00000584865.5:n.308G=
NM_000789.3:c.2362G=	NP_000780.1:p.Glu788=
NM_001178057.1:c.640G=	NP_001171528.1:p.Glu214=
NM_152830.2:c.640G=	NP_690043.1:p.Glu214=
XM_005257110.1:c.1813G=	XP_005257167.1:p.Glu605=
XM_006721737.2:c.700G=	XP_006721800.2:p.Glu234=
XM_006721737.3:c.700G=	XP_006721800.2:p.Glu234=
NM_000789.4:c.2362G= MANE Select	NP_000780.1:p.Glu788=
NM_001178057.2:c.640G=	NP_001171528.1:p.Glu214=
NM_152830.3:c.640G=	NP_690043.1:p.Glu214=
NM_001382700.1:c.1795G=	NP_001369629.1:p.Glu599=
NM_001382701.1:c.1510G=	NP_001369630.1:p.Glu504=
NM_001382702.1:c.292G=	NP_001369631.1:p.Glu98=
NR_168483.1:n.740G=