Canonical Allele Identifier: CA2269949980

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497165C= , CM000679.2:g.63497165C=	GRCh38
NC_000017.10:g.61574526C= , CM000679.1:g.61574526C=	GRCh37
NC_000017.9:g.58928258C=	NCBI36
NG_011648.1:g.25093C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3720C= MANE Select	ENSP00000290866.4:p.Ser1240=
ENST00000290863.10:c.1998C=	ENSP00000290863.6:p.Ser666=
ENST00000290866.9:c.3720C=	ENSP00000290866.4:p.Ser1240=
ENST00000413513.7:c.1875C=	ENSP00000392247.3:p.Ser625=
ENST00000428043.5:c.*142C=	ENSP00000397593.2:n.*142C=
ENST00000577647.2:c.1969+180C=	ENSP00000464149.1:n.1969+180C=
ENST00000578839.5:c.*1475C=	ENSP00000462110.2:n.*1475C=
ENST00000579314.5:c.*1449C=	ENSP00000462599.1:n.*1449C=
NM_000789.3:c.3720C=	NP_000780.1:p.Ser1240=
NM_001178057.1:c.1875C=	NP_001171528.1:p.Ser625=
NM_152830.2:c.1998C=	NP_690043.1:p.Ser666=
XM_005257110.1:c.3171C=	XP_005257167.1:p.Ser1057=
XM_006721737.2:c.2058C=	XP_006721800.2:p.Ser686=
XM_006721737.3:c.2058C=	XP_006721800.2:p.Ser686=
NM_000789.4:c.3720C= MANE Select	NP_000780.1:p.Ser1240=
NM_001178057.2:c.1875C=	NP_001171528.1:p.Ser625=
NM_152830.3:c.1998C=	NP_690043.1:p.Ser666=
NM_001382700.1:c.3153C=	NP_001369629.1:p.Ser1051=
NM_001382701.1:c.2868C=	NP_001369630.1:p.Ser956=
NM_001382702.1:c.1335C=	NP_001369631.1:p.Ser445=
NR_168483.1:n.2098C=