Canonical Allele Identifier: CA400568497
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs963984458

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497180C>A , CM000679.2:g.63497180C>A GRCh38
NC_000017.10:g.61574541C>A , CM000679.1:g.61574541C>A GRCh37
NC_000017.9:g.58928273C>A NCBI36
NG_011648.1:g.25108C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3735C>A MANE Select ENSP00000290866.4:p.Phe1245Leu
ENST00000290863.10:c.2013C>A ENSP00000290863.6:p.Phe671Leu
ENST00000290866.9:c.3735C>A ENSP00000290866.4:p.Phe1245Leu
ENST00000413513.7:c.1890C>A ENSP00000392247.3:p.Phe630Leu
ENST00000428043.5:c.*157C>A ENSP00000397593.2:n.*157C>A
ENST00000577647.2:c.1969+195C>A ENSP00000464149.1:n.1969+195C>A
ENST00000578839.5:c.*1490C>A ENSP00000462110.2:n.*1490C>A
ENST00000579314.5:c.*1464C>A ENSP00000462599.1:n.*1464C>A
NM_000789.3:c.3735C>A NP_000780.1:p.Phe1245Leu
NM_001178057.1:c.1890C>A NP_001171528.1:p.Phe630Leu
NM_152830.2:c.2013C>A NP_690043.1:p.Phe671Leu
XM_005257110.1:c.3186C>A XP_005257167.1:p.Phe1062Leu
XM_006721737.2:c.2073C>A XP_006721800.2:p.Phe691Leu
XM_006721737.3:c.2073C>A XP_006721800.2:p.Phe691Leu
NM_000789.4:c.3735C>A MANE Select NP_000780.1:p.Phe1245Leu
NM_001178057.2:c.1890C>A NP_001171528.1:p.Phe630Leu
NM_152830.3:c.2013C>A NP_690043.1:p.Phe671Leu
NM_001382700.1:c.3168C>A NP_001369629.1:p.Phe1056Leu
NM_001382701.1:c.2883C>A NP_001369630.1:p.Phe961Leu
NM_001382702.1:c.1350C>A NP_001369631.1:p.Phe450Leu
NR_168483.1:n.2113C>A