Canonical Allele Identifier: CA2269950033

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497276C= , CM000679.2:g.63497276C=	GRCh38
NC_000017.10:g.61574637C= , CM000679.1:g.61574637C=	GRCh37
NC_000017.9:g.58928369C=	NCBI36
NG_011648.1:g.25204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3831C= MANE Select	ENSP00000290866.4:p.Ser1277=
ENST00000290863.10:c.2109C=	ENSP00000290863.6:p.Ser703=
ENST00000290866.9:c.3831C=	ENSP00000290866.4:p.Ser1277=
ENST00000413513.7:c.1986C=	ENSP00000392247.3:p.Ser662=
ENST00000428043.5:c.*253C=	ENSP00000397593.2:n.*253C=
ENST00000577647.2:c.1969+291C=	ENSP00000464149.1:n.1969+291C=
ENST00000578839.5:c.*1586C=	ENSP00000462110.2:n.*1586C=
ENST00000579314.5:c.*1560C=	ENSP00000462599.1:n.*1560C=
NM_000789.3:c.3831C=	NP_000780.1:p.Ser1277=
NM_001178057.1:c.1986C=	NP_001171528.1:p.Ser662=
NM_152830.2:c.2109C=	NP_690043.1:p.Ser703=
XM_005257110.1:c.3282C=	XP_005257167.1:p.Ser1094=
XM_006721737.2:c.2169C=	XP_006721800.2:p.Ser723=
XM_006721737.3:c.2169C=	XP_006721800.2:p.Ser723=
NM_000789.4:c.3831C= MANE Select	NP_000780.1:p.Ser1277=
NM_001178057.2:c.1986C=	NP_001171528.1:p.Ser662=
NM_152830.3:c.2109C=	NP_690043.1:p.Ser703=
NM_001382700.1:c.3264C=	NP_001369629.1:p.Ser1088=
NM_001382701.1:c.2979C=	NP_001369630.1:p.Ser993=
NM_001382702.1:c.1446C=	NP_001369631.1:p.Ser482=
NR_168483.1:n.2209C=