Canonical Allele Identifier: CA400569181
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1393052928

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63497287T>C , CM000679.2:g.63497287T>C GRCh38
NC_000017.10:g.61574648T>C , CM000679.1:g.61574648T>C GRCh37
NC_000017.9:g.58928380T>C NCBI36
NG_011648.1:g.25215T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.3842T>C MANE Select ENSP00000290866.4:p.Phe1281Ser
ENST00000290863.10:c.2120T>C ENSP00000290863.6:p.Phe707Ser
ENST00000290866.9:c.3842T>C ENSP00000290866.4:p.Phe1281Ser
ENST00000413513.7:c.1997T>C ENSP00000392247.3:p.Phe666Ser
ENST00000428043.5:c.*264T>C ENSP00000397593.2:n.*264T>C
ENST00000577647.2:c.1969+302T>C ENSP00000464149.1:n.1969+302T>C
ENST00000578839.5:c.*1597T>C ENSP00000462110.2:n.*1597T>C
ENST00000579314.5:c.*1571T>C ENSP00000462599.1:n.*1571T>C
NM_000789.3:c.3842T>C NP_000780.1:p.Phe1281Ser
NM_001178057.1:c.1997T>C NP_001171528.1:p.Phe666Ser
NM_152830.2:c.2120T>C NP_690043.1:p.Phe707Ser
XM_005257110.1:c.3293T>C XP_005257167.1:p.Phe1098Ser
XM_006721737.2:c.2180T>C XP_006721800.2:p.Phe727Ser
XM_006721737.3:c.2180T>C XP_006721800.2:p.Phe727Ser
NM_000789.4:c.3842T>C MANE Select NP_000780.1:p.Phe1281Ser
NM_001178057.2:c.1997T>C NP_001171528.1:p.Phe666Ser
NM_152830.3:c.2120T>C NP_690043.1:p.Phe707Ser
NM_001382700.1:c.3275T>C NP_001369629.1:p.Phe1092Ser
NM_001382701.1:c.2990T>C NP_001369630.1:p.Phe997Ser
NM_001382702.1:c.1457T>C NP_001369631.1:p.Phe486Ser
NR_168483.1:n.2220T>C