Canonical Allele Identifier: CA2269950032

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497270C= , CM000679.2:g.63497270C=	GRCh38
NC_000017.10:g.61574631C= , CM000679.1:g.61574631C=	GRCh37
NC_000017.9:g.58928363C=	NCBI36
NG_011648.1:g.25198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3825C= MANE Select	ENSP00000290866.4:p.Gly1275=
ENST00000290863.10:c.2103C=	ENSP00000290863.6:p.Gly701=
ENST00000290866.9:c.3825C=	ENSP00000290866.4:p.Gly1275=
ENST00000413513.7:c.1980C=	ENSP00000392247.3:p.Gly660=
ENST00000428043.5:c.*247C=	ENSP00000397593.2:n.*247C=
ENST00000577647.2:c.1969+285C=	ENSP00000464149.1:n.1969+285C=
ENST00000578839.5:c.*1580C=	ENSP00000462110.2:n.*1580C=
ENST00000579314.5:c.*1554C=	ENSP00000462599.1:n.*1554C=
NM_000789.3:c.3825C=	NP_000780.1:p.Gly1275=
NM_001178057.1:c.1980C=	NP_001171528.1:p.Gly660=
NM_152830.2:c.2103C=	NP_690043.1:p.Gly701=
XM_005257110.1:c.3276C=	XP_005257167.1:p.Gly1092=
XM_006721737.2:c.2163C=	XP_006721800.2:p.Gly721=
XM_006721737.3:c.2163C=	XP_006721800.2:p.Gly721=
NM_000789.4:c.3825C= MANE Select	NP_000780.1:p.Gly1275=
NM_001178057.2:c.1980C=	NP_001171528.1:p.Gly660=
NM_152830.3:c.2103C=	NP_690043.1:p.Gly701=
NM_001382700.1:c.3258C=	NP_001369629.1:p.Gly1086=
NM_001382701.1:c.2973C=	NP_001369630.1:p.Gly991=
NM_001382702.1:c.1440C=	NP_001369631.1:p.Gly480=
NR_168483.1:n.2203C=