Canonical Allele Identifier: CA2269949981

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497166G= , CM000679.2:g.63497166G=	GRCh38
NC_000017.10:g.61574527G= , CM000679.1:g.61574527G=	GRCh37
NC_000017.9:g.58928259G=	NCBI36
NG_011648.1:g.25094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3721G= MANE Select	ENSP00000290866.4:p.Gly1241=
ENST00000290863.10:c.1999G=	ENSP00000290863.6:p.Gly667=
ENST00000290866.9:c.3721G=	ENSP00000290866.4:p.Gly1241=
ENST00000413513.7:c.1876G=	ENSP00000392247.3:p.Gly626=
ENST00000428043.5:c.*143G=	ENSP00000397593.2:n.*143G=
ENST00000577647.2:c.1969+181G=	ENSP00000464149.1:n.1969+181G=
ENST00000578839.5:c.*1476G=	ENSP00000462110.2:n.*1476G=
ENST00000579314.5:c.*1450G=	ENSP00000462599.1:n.*1450G=
NM_000789.3:c.3721G=	NP_000780.1:p.Gly1241=
NM_001178057.1:c.1876G=	NP_001171528.1:p.Gly626=
NM_152830.2:c.1999G=	NP_690043.1:p.Gly667=
XM_005257110.1:c.3172G=	XP_005257167.1:p.Gly1058=
XM_006721737.2:c.2059G=	XP_006721800.2:p.Gly687=
XM_006721737.3:c.2059G=	XP_006721800.2:p.Gly687=
NM_000789.4:c.3721G= MANE Select	NP_000780.1:p.Gly1241=
NM_001178057.2:c.1876G=	NP_001171528.1:p.Gly626=
NM_152830.3:c.1999G=	NP_690043.1:p.Gly667=
NM_001382700.1:c.3154G=	NP_001369629.1:p.Gly1052=
NM_001382701.1:c.2869G=	NP_001369630.1:p.Gly957=
NM_001382702.1:c.1336G=	NP_001369631.1:p.Gly446=
NR_168483.1:n.2099G=