Canonical Allele Identifier: CA2269950072

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497337G= , CM000679.2:g.63497337G=	GRCh38
NC_000017.10:g.61574698G= , CM000679.1:g.61574698G=	GRCh37
NC_000017.9:g.58928430G=	NCBI36
NG_011648.1:g.25265G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3892G= MANE Select	ENSP00000290866.4:p.Gly1298=
ENST00000290863.10:c.2170G=	ENSP00000290863.6:p.Gly724=
ENST00000290866.9:c.3892G=	ENSP00000290866.4:p.Gly1298=
ENST00000413513.7:c.2047G=	ENSP00000392247.3:p.Gly683=
ENST00000428043.5:c.*314G=	ENSP00000397593.2:n.*314G=
ENST00000577647.2:c.1969+352G=	ENSP00000464149.1:n.1969+352G=
ENST00000578839.5:c.*1647G=	ENSP00000462110.2:n.*1647G=
ENST00000579314.5:c.*1621G=	ENSP00000462599.1:n.*1621G=
NM_000789.3:c.3892G=	NP_000780.1:p.Gly1298=
NM_001178057.1:c.2047G=	NP_001171528.1:p.Gly683=
NM_152830.2:c.2170G=	NP_690043.1:p.Gly724=
XM_005257110.1:c.3343G=	XP_005257167.1:p.Gly1115=
XM_006721737.2:c.2230G=	XP_006721800.2:p.Gly744=
XM_006721737.3:c.2230G=	XP_006721800.2:p.Gly744=
NM_000789.4:c.3892G= MANE Select	NP_000780.1:p.Gly1298=
NM_001178057.2:c.2047G=	NP_001171528.1:p.Gly683=
NM_152830.3:c.2170G=	NP_690043.1:p.Gly724=
NM_001382700.1:c.3325G=	NP_001369629.1:p.Gly1109=
NM_001382701.1:c.3040G=	NP_001369630.1:p.Gly1014=
NM_001382702.1:c.1507G=	NP_001369631.1:p.Gly503=
NR_168483.1:n.2270G=