Canonical Allele Identifier: CA2269950009

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497219C= , CM000679.2:g.63497219C=	GRCh38
NC_000017.10:g.61574580C= , CM000679.1:g.61574580C=	GRCh37
NC_000017.9:g.58928312C=	NCBI36
NG_011648.1:g.25147C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3774C= MANE Select	ENSP00000290866.4:p.Gly1258=
ENST00000290863.10:c.2052C=	ENSP00000290863.6:p.Gly684=
ENST00000290866.9:c.3774C=	ENSP00000290866.4:p.Gly1258=
ENST00000413513.7:c.1929C=	ENSP00000392247.3:p.Gly643=
ENST00000428043.5:c.*196C=	ENSP00000397593.2:n.*196C=
ENST00000577647.2:c.1969+234C=	ENSP00000464149.1:n.1969+234C=
ENST00000578839.5:c.*1529C=	ENSP00000462110.2:n.*1529C=
ENST00000579314.5:c.*1503C=	ENSP00000462599.1:n.*1503C=
NM_000789.3:c.3774C=	NP_000780.1:p.Gly1258=
NM_001178057.1:c.1929C=	NP_001171528.1:p.Gly643=
NM_152830.2:c.2052C=	NP_690043.1:p.Gly684=
XM_005257110.1:c.3225C=	XP_005257167.1:p.Gly1075=
XM_006721737.2:c.2112C=	XP_006721800.2:p.Gly704=
XM_006721737.3:c.2112C=	XP_006721800.2:p.Gly704=
NM_000789.4:c.3774C= MANE Select	NP_000780.1:p.Gly1258=
NM_001178057.2:c.1929C=	NP_001171528.1:p.Gly643=
NM_152830.3:c.2052C=	NP_690043.1:p.Gly684=
NM_001382700.1:c.3207C=	NP_001369629.1:p.Gly1069=
NM_001382701.1:c.2922C=	NP_001369630.1:p.Gly974=
NM_001382702.1:c.1389C=	NP_001369631.1:p.Gly463=
NR_168483.1:n.2152C=