Canonical Allele Identifier: CA2269949849

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496983C= , CM000679.2:g.63496983C=	GRCh38
NC_000017.10:g.61574344C= , CM000679.1:g.61574344C=	GRCh37
NC_000017.9:g.58928076C=	NCBI36
NG_011648.1:g.24911C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.3689C= MANE Select	ENSP00000290866.4:p.Ser1230=
ENST00000290863.10:c.1967C=	ENSP00000290863.6:p.Ser656=
ENST00000290866.9:c.3689C=	ENSP00000290866.4:p.Ser1230=
ENST00000413513.7:c.1844C=	ENSP00000392247.3:p.Ser615=
ENST00000428043.5:c.3689C=	ENSP00000397593.2:p.Ser1230=
ENST00000577418.5:n.699C=
ENST00000577647.2:c.1967C=	ENSP00000464149.1:p.Ser656=
ENST00000578839.5:c.*1444C=	ENSP00000462110.2:n.*1444C=
ENST00000579314.5:c.*1418C=	ENSP00000462599.1:n.*1418C=
ENST00000579409.1:c.376C=
ENST00000582244.1:n.563C=
NM_000789.3:c.3689C=	NP_000780.1:p.Ser1230=
NM_001178057.1:c.1844C=	NP_001171528.1:p.Ser615=
NM_152830.2:c.1967C=	NP_690043.1:p.Ser656=
XM_005257110.1:c.3140C=	XP_005257167.1:p.Ser1047=
XM_006721737.2:c.2027C=	XP_006721800.2:p.Ser676=
XM_006721737.3:c.2027C=	XP_006721800.2:p.Ser676=
NM_000789.4:c.3689C= MANE Select	NP_000780.1:p.Ser1230=
NM_001178057.2:c.1844C=	NP_001171528.1:p.Ser615=
NM_152830.3:c.1967C=	NP_690043.1:p.Ser656=
NM_001382700.1:c.3122C=	NP_001369629.1:p.Ser1041=
NM_001382701.1:c.2837C=	NP_001369630.1:p.Ser946=
NM_001382702.1:c.1304C=	NP_001369631.1:p.Ser435=
NR_168483.1:n.2067C=