Canonical Allele Identifier: CA400557850
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488680T>G , CM000679.2:g.63488680T>G GRCh38
NC_000017.10:g.61566041T>G , CM000679.1:g.61566041T>G GRCh37
NC_000017.9:g.58919773T>G NCBI36
NG_011648.1:g.16608T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2338T>G MANE Select ENSP00000290866.4:p.Tyr780Asp
ENST00000290863.10:c.616T>G ENSP00000290863.6:p.Tyr206Asp
ENST00000290866.9:c.2338T>G ENSP00000290866.4:p.Tyr780Asp
ENST00000413513.7:c.616T>G ENSP00000392247.3:p.Tyr206Asp
ENST00000428043.5:c.2338T>G ENSP00000397593.2:p.Tyr780Asp
ENST00000577647.2:c.616T>G ENSP00000464149.1:p.Tyr206Asp
ENST00000578839.5:c.*408T>G ENSP00000462110.2:n.*408T>G
ENST00000579204.1:c.597T>G ENSP00000464629.1:n.597T>G
ENST00000579314.5:c.*67T>G ENSP00000462599.1:n.*67T>G
ENST00000582005.5:c.*258T>G ENSP00000462002.1:n.*258T>G
ENST00000582761.1:c.106T>G ENSP00000462909.1:p.Tyr36Asp
ENST00000584865.5:n.284T>G
NM_000789.3:c.2338T>G NP_000780.1:p.Tyr780Asp
NM_001178057.1:c.616T>G NP_001171528.1:p.Tyr206Asp
NM_152830.2:c.616T>G NP_690043.1:p.Tyr206Asp
XM_005257110.1:c.1789T>G XP_005257167.1:p.Tyr597Asp
XM_006721737.2:c.676T>G XP_006721800.2:p.Tyr226Asp
XM_006721737.3:c.676T>G XP_006721800.2:p.Tyr226Asp
NM_000789.4:c.2338T>G MANE Select NP_000780.1:p.Tyr780Asp
NM_001178057.2:c.616T>G NP_001171528.1:p.Tyr206Asp
NM_152830.3:c.616T>G NP_690043.1:p.Tyr206Asp
NM_001382700.1:c.1771T>G NP_001369629.1:p.Tyr591Asp
NM_001382701.1:c.1486T>G NP_001369630.1:p.Tyr496Asp
NM_001382702.1:c.268T>G NP_001369631.1:p.Tyr90Asp
NR_168483.1:n.716T>G