Canonical Allele Identifier: CA2269945927

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488650C= , CM000679.2:g.63488650C=	GRCh38
NC_000017.10:g.61566011C= , CM000679.1:g.61566011C=	GRCh37
NC_000017.9:g.58919743C=	NCBI36
NG_011648.1:g.16578C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2308C= MANE Select	ENSP00000290866.4:p.Leu770=
ENST00000290863.10:c.586C=	ENSP00000290863.6:p.Leu196=
ENST00000290866.9:c.2308C=	ENSP00000290866.4:p.Leu770=
ENST00000413513.7:c.586C=	ENSP00000392247.3:p.Leu196=
ENST00000428043.5:c.2308C=	ENSP00000397593.2:p.Leu770=
ENST00000577647.2:c.586C=	ENSP00000464149.1:p.Leu196=
ENST00000578839.5:c.*378C=	ENSP00000462110.2:n.*378C=
ENST00000579204.1:c.567C=	ENSP00000464629.1:n.567C=
ENST00000579314.5:c.*37C=	ENSP00000462599.1:n.*37C=
ENST00000582005.5:c.*228C=	ENSP00000462002.1:n.*228C=
ENST00000582761.1:c.76C=	ENSP00000462909.1:p.Leu26=
ENST00000584865.5:n.254C=
NM_000789.3:c.2308C=	NP_000780.1:p.Leu770=
NM_001178057.1:c.586C=	NP_001171528.1:p.Leu196=
NM_152830.2:c.586C=	NP_690043.1:p.Leu196=
XM_005257110.1:c.1759C=	XP_005257167.1:p.Leu587=
XM_006721737.2:c.646C=	XP_006721800.2:p.Leu216=
XM_006721737.3:c.646C=	XP_006721800.2:p.Leu216=
NM_000789.4:c.2308C= MANE Select	NP_000780.1:p.Leu770=
NM_001178057.2:c.586C=	NP_001171528.1:p.Leu196=
NM_152830.3:c.586C=	NP_690043.1:p.Leu196=
NM_001382700.1:c.1741C=	NP_001369629.1:p.Leu581=
NM_001382701.1:c.1456C=	NP_001369630.1:p.Leu486=
NM_001382702.1:c.238C=	NP_001369631.1:p.Leu80=
NR_168483.1:n.686C=