Canonical Allele Identifier: CA2269944893

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486711A= , CM000679.2:g.63486711A=	GRCh38
NC_000017.10:g.61564072A= , CM000679.1:g.61564072A=	GRCh37
NC_000017.9:g.58917804A=	NCBI36
NG_011648.1:g.14639A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2213A= MANE Select	ENSP00000290866.4:p.Glu738=
ENST00000290863.10:c.491A=	ENSP00000290863.6:p.Glu164=
ENST00000290866.9:c.2213A=	ENSP00000290866.4:p.Glu738=
ENST00000413513.7:c.491A=	ENSP00000392247.3:p.Glu164=
ENST00000428043.5:c.2213A=	ENSP00000397593.2:p.Glu738=
ENST00000577647.2:c.491A=	ENSP00000464149.1:p.Glu164=
ENST00000578839.5:c.*283A=	ENSP00000462110.2:n.*283A=
ENST00000579204.1:c.394A=	ENSP00000464629.1:n.394A=
ENST00000579314.5:c.491A=	ENSP00000462599.1:p.Glu164=
ENST00000579726.5:c.775A=
ENST00000582005.5:c.*133A=	ENSP00000462002.1:n.*133A=
NM_000789.3:c.2213A=	NP_000780.1:p.Glu738=
NM_001178057.1:c.491A=	NP_001171528.1:p.Glu164=
NM_152830.2:c.491A=	NP_690043.1:p.Glu164=
XM_005257110.1:c.1664A=	XP_005257167.1:p.Glu555=
XM_006721737.2:c.551A=	XP_006721800.2:p.Glu184=
XM_006721737.3:c.551A=	XP_006721800.2:p.Glu184=
NM_000789.4:c.2213A= MANE Select	NP_000780.1:p.Glu738=
NM_001178057.2:c.491A=	NP_001171528.1:p.Glu164=
NM_152830.3:c.491A=	NP_690043.1:p.Glu164=
NM_001382700.1:c.1646A=	NP_001369629.1:p.Glu549=
NM_001382701.1:c.1361A=	NP_001369630.1:p.Glu454=
NM_001382702.1:c.143A=	NP_001369631.1:p.Glu48=
NR_168483.1:n.513A=