Canonical Allele Identifier: CA2269949794
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63496894C= , CM000679.2:g.63496894C= GRCh38
NC_000017.10:g.61574255C= , CM000679.1:g.61574255C= GRCh37
NC_000017.9:g.58927987C= NCBI36
NG_011648.1:g.24822C=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.3600C= MANE Select ENSP00000290866.4:p.Tyr1200=
ENST00000290863.10:c.1878C= ENSP00000290863.6:p.Tyr626=
ENST00000290866.9:c.3600C= ENSP00000290866.4:p.Tyr1200=
ENST00000413513.7:c.1755C= ENSP00000392247.3:p.Tyr585=
ENST00000428043.5:c.3600C= ENSP00000397593.2:p.Tyr1200=
ENST00000577418.5:n.610C=
ENST00000577647.2:c.1878C= ENSP00000464149.1:p.Tyr626=
ENST00000578839.5:c.*1355C= ENSP00000462110.2:n.*1355C=
ENST00000579314.5:c.*1329C= ENSP00000462599.1:n.*1329C=
ENST00000579409.1:c.287C=
ENST00000582244.1:n.474C=
NM_000789.3:c.3600C= NP_000780.1:p.Tyr1200=
NM_001178057.1:c.1755C= NP_001171528.1:p.Tyr585=
NM_152830.2:c.1878C= NP_690043.1:p.Tyr626=
XM_005257110.1:c.3051C= XP_005257167.1:p.Tyr1017=
XM_006721737.2:c.1938C= XP_006721800.2:p.Tyr646=
XM_006721737.3:c.1938C= XP_006721800.2:p.Tyr646=
NM_000789.4:c.3600C= MANE Select NP_000780.1:p.Tyr1200=
NM_001178057.2:c.1755C= NP_001171528.1:p.Tyr585=
NM_152830.3:c.1878C= NP_690043.1:p.Tyr626=
NM_001382700.1:c.3033C= NP_001369629.1:p.Tyr1011=
NM_001382701.1:c.2748C= NP_001369630.1:p.Tyr916=
NM_001382702.1:c.1215C= NP_001369631.1:p.Tyr405=
NR_168483.1:n.1978C=