Canonical Allele Identifier: CA400557852
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488681A>T , CM000679.2:g.63488681A>T GRCh38
NC_000017.10:g.61566042A>T , CM000679.1:g.61566042A>T GRCh37
NC_000017.9:g.58919774A>T NCBI36
NG_011648.1:g.16609A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2339A>T MANE Select ENSP00000290866.4:p.Tyr780Phe
ENST00000290863.10:c.617A>T ENSP00000290863.6:p.Tyr206Phe
ENST00000290866.9:c.2339A>T ENSP00000290866.4:p.Tyr780Phe
ENST00000413513.7:c.617A>T ENSP00000392247.3:p.Tyr206Phe
ENST00000428043.5:c.2339A>T ENSP00000397593.2:p.Tyr780Phe
ENST00000577647.2:c.617A>T ENSP00000464149.1:p.Tyr206Phe
ENST00000578839.5:c.*409A>T ENSP00000462110.2:n.*409A>T
ENST00000579204.1:c.598A>T ENSP00000464629.1:n.598A>T
ENST00000579314.5:c.*68A>T ENSP00000462599.1:n.*68A>T
ENST00000582005.5:c.*259A>T ENSP00000462002.1:n.*259A>T
ENST00000582761.1:c.107A>T ENSP00000462909.1:p.Tyr36Phe
ENST00000584865.5:n.285A>T
NM_000789.3:c.2339A>T NP_000780.1:p.Tyr780Phe
NM_001178057.1:c.617A>T NP_001171528.1:p.Tyr206Phe
NM_152830.2:c.617A>T NP_690043.1:p.Tyr206Phe
XM_005257110.1:c.1790A>T XP_005257167.1:p.Tyr597Phe
XM_006721737.2:c.677A>T XP_006721800.2:p.Tyr226Phe
XM_006721737.3:c.677A>T XP_006721800.2:p.Tyr226Phe
NM_000789.4:c.2339A>T MANE Select NP_000780.1:p.Tyr780Phe
NM_001178057.2:c.617A>T NP_001171528.1:p.Tyr206Phe
NM_152830.3:c.617A>T NP_690043.1:p.Tyr206Phe
NM_001382700.1:c.1772A>T NP_001369629.1:p.Tyr591Phe
NM_001382701.1:c.1487A>T NP_001369630.1:p.Tyr496Phe
NM_001382702.1:c.269A>T NP_001369631.1:p.Tyr90Phe
NR_168483.1:n.717A>T