Canonical Allele Identifier: CA400540851
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63478067C>A , CM000679.2:g.63478067C>A GRCh38
NC_000017.10:g.61555428C>A , CM000679.1:g.61555428C>A GRCh37
NC_000017.9:g.58909160C>A NCBI36
NG_011648.1:g.5995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.386C>A MANE Select ENSP00000290866.4:p.Ser129Tyr
ENST00000290866.9:c.386C>A ENSP00000290866.4:p.Ser129Tyr
ENST00000428043.5:c.386C>A ENSP00000397593.2:p.Ser129Tyr
ENST00000579462.1:n.411C>A
ENST00000580318.1:n.575C>A
ENST00000582627.1:c.386C>A ENSP00000462280.1:p.Ser129Tyr
ENST00000582678.5:c.386C>A ENSP00000462995.1:p.Ser129Tyr
ENST00000583336.5:n.420C>A
ENST00000584529.5:n.420C>A
NM_000789.3:c.386C>A NP_000780.1:p.Ser129Tyr
XM_005257110.1:c.-70C>A XP_005257167.1:n.-70C>A
NM_000789.4:c.386C>A MANE Select NP_000780.1:p.Ser129Tyr
NM_001382700.1:c.151C>A NP_001369629.1:p.Leu51Met
NM_001382701.1:c.-229C>A NP_001369630.1:n.-229C>A