Canonical Allele Identifier: CA501342413
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1402919954

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497276C>T , CM000679.2:g.63497276C>T GRCh38
NC_000017.10:g.61574637C>T , CM000679.1:g.61574637C>T GRCh37
NC_000017.9:g.58928369C>T NCBI36
NG_011648.1:g.25204C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3831C>T MANE Select ENSP00000290866.4:p.Ser1277=
ENST00000290863.10:c.2109C>T ENSP00000290863.6:p.Ser703=
ENST00000290866.9:c.3831C>T ENSP00000290866.4:p.Ser1277=
ENST00000413513.7:c.1986C>T ENSP00000392247.3:p.Ser662=
ENST00000428043.5:c.*253C>T ENSP00000397593.2:n.*253C>T
ENST00000577647.2:c.1969+291C>T ENSP00000464149.1:n.1969+291C>T
ENST00000578839.5:c.*1586C>T ENSP00000462110.2:n.*1586C>T
ENST00000579314.5:c.*1560C>T ENSP00000462599.1:n.*1560C>T
NM_000789.3:c.3831C>T NP_000780.1:p.Ser1277=
NM_001178057.1:c.1986C>T NP_001171528.1:p.Ser662=
NM_152830.2:c.2109C>T NP_690043.1:p.Ser703=
XM_005257110.1:c.3282C>T XP_005257167.1:p.Ser1094=
XM_006721737.2:c.2169C>T XP_006721800.2:p.Ser723=
XM_006721737.3:c.2169C>T XP_006721800.2:p.Ser723=
NM_000789.4:c.3831C>T MANE Select NP_000780.1:p.Ser1277=
NM_001178057.2:c.1986C>T NP_001171528.1:p.Ser662=
NM_152830.3:c.2109C>T NP_690043.1:p.Ser703=
NM_001382700.1:c.3264C>T NP_001369629.1:p.Ser1088=
NM_001382701.1:c.2979C>T NP_001369630.1:p.Ser993=
NM_001382702.1:c.1446C>T NP_001369631.1:p.Ser482=
NR_168483.1:n.2209C>T