Canonical Allele Identifier: CA501342293

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497177C>T , CM000679.2:g.63497177C>T	GRCh38
NC_000017.10:g.61574538C>T , CM000679.1:g.61574538C>T	GRCh37
NC_000017.9:g.58928270C>T	NCBI36
NG_011648.1:g.25105C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3732C>T MANE Select	ENSP00000290866.4:p.Ser1244=
ENST00000290863.10:c.2010C>T	ENSP00000290863.6:p.Ser670=
ENST00000290866.9:c.3732C>T	ENSP00000290866.4:p.Ser1244=
ENST00000413513.7:c.1887C>T	ENSP00000392247.3:p.Ser629=
ENST00000428043.5:c.*154C>T	ENSP00000397593.2:n.*154C>T
ENST00000577647.2:c.1969+192C>T	ENSP00000464149.1:n.1969+192C>T
ENST00000578839.5:c.*1487C>T	ENSP00000462110.2:n.*1487C>T
ENST00000579314.5:c.*1461C>T	ENSP00000462599.1:n.*1461C>T
NM_000789.3:c.3732C>T	NP_000780.1:p.Ser1244=
NM_001178057.1:c.1887C>T	NP_001171528.1:p.Ser629=
NM_152830.2:c.2010C>T	NP_690043.1:p.Ser670=
XM_005257110.1:c.3183C>T	XP_005257167.1:p.Ser1061=
XM_006721737.2:c.2070C>T	XP_006721800.2:p.Ser690=
XM_006721737.3:c.2070C>T	XP_006721800.2:p.Ser690=
NM_000789.4:c.3732C>T MANE Select	NP_000780.1:p.Ser1244=
NM_001178057.2:c.1887C>T	NP_001171528.1:p.Ser629=
NM_152830.3:c.2010C>T	NP_690043.1:p.Ser670=
NM_001382700.1:c.3165C>T	NP_001369629.1:p.Ser1055=
NM_001382701.1:c.2880C>T	NP_001369630.1:p.Ser960=
NM_001382702.1:c.1347C>T	NP_001369631.1:p.Ser449=
NR_168483.1:n.2110C>T