Canonical Allele Identifier: CA2269950046

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497304A= , CM000679.2:g.63497304A=	GRCh38
NC_000017.10:g.61574665A= , CM000679.1:g.61574665A=	GRCh37
NC_000017.9:g.58928397A=	NCBI36
NG_011648.1:g.25232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3859A= MANE Select	ENSP00000290866.4:p.Ser1287=
ENST00000290863.10:c.2137A=	ENSP00000290863.6:p.Ser713=
ENST00000290866.9:c.3859A=	ENSP00000290866.4:p.Ser1287=
ENST00000413513.7:c.2014A=	ENSP00000392247.3:p.Ser672=
ENST00000428043.5:c.*281A=	ENSP00000397593.2:n.*281A=
ENST00000577647.2:c.1969+319A=	ENSP00000464149.1:n.1969+319A=
ENST00000578839.5:c.*1614A=	ENSP00000462110.2:n.*1614A=
ENST00000579314.5:c.*1588A=	ENSP00000462599.1:n.*1588A=
NM_000789.3:c.3859A=	NP_000780.1:p.Ser1287=
NM_001178057.1:c.2014A=	NP_001171528.1:p.Ser672=
NM_152830.2:c.2137A=	NP_690043.1:p.Ser713=
XM_005257110.1:c.3310A=	XP_005257167.1:p.Ser1104=
XM_006721737.2:c.2197A=	XP_006721800.2:p.Ser733=
XM_006721737.3:c.2197A=	XP_006721800.2:p.Ser733=
NM_000789.4:c.3859A= MANE Select	NP_000780.1:p.Ser1287=
NM_001178057.2:c.2014A=	NP_001171528.1:p.Ser672=
NM_152830.3:c.2137A=	NP_690043.1:p.Ser713=
NM_001382700.1:c.3292A=	NP_001369629.1:p.Ser1098=
NM_001382701.1:c.3007A=	NP_001369630.1:p.Ser1003=
NM_001382702.1:c.1474A=	NP_001369631.1:p.Ser492=
NR_168483.1:n.2237A=