Canonical Allele Identifier: CA2269949991

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497185G= , CM000679.2:g.63497185G=	GRCh38
NC_000017.10:g.61574546G= , CM000679.1:g.61574546G=	GRCh37
NC_000017.9:g.58928278G=	NCBI36
NG_011648.1:g.25113G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3740G= MANE Select	ENSP00000290866.4:p.Gly1247=
ENST00000290863.10:c.2018G=	ENSP00000290863.6:p.Gly673=
ENST00000290866.9:c.3740G=	ENSP00000290866.4:p.Gly1247=
ENST00000413513.7:c.1895G=	ENSP00000392247.3:p.Gly632=
ENST00000428043.5:c.*162G=	ENSP00000397593.2:n.*162G=
ENST00000577647.2:c.1969+200G=	ENSP00000464149.1:n.1969+200G=
ENST00000578839.5:c.*1495G=	ENSP00000462110.2:n.*1495G=
ENST00000579314.5:c.*1469G=	ENSP00000462599.1:n.*1469G=
NM_000789.3:c.3740G=	NP_000780.1:p.Gly1247=
NM_001178057.1:c.1895G=	NP_001171528.1:p.Gly632=
NM_152830.2:c.2018G=	NP_690043.1:p.Gly673=
XM_005257110.1:c.3191G=	XP_005257167.1:p.Gly1064=
XM_006721737.2:c.2078G=	XP_006721800.2:p.Gly693=
XM_006721737.3:c.2078G=	XP_006721800.2:p.Gly693=
NM_000789.4:c.3740G= MANE Select	NP_000780.1:p.Gly1247=
NM_001178057.2:c.1895G=	NP_001171528.1:p.Gly632=
NM_152830.3:c.2018G=	NP_690043.1:p.Gly673=
NM_001382700.1:c.3173G=	NP_001369629.1:p.Gly1058=
NM_001382701.1:c.2888G=	NP_001369630.1:p.Gly963=
NM_001382702.1:c.1355G=	NP_001369631.1:p.Gly452=
NR_168483.1:n.2118G=