Canonical Allele Identifier: CA400540889
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63478087A>C , CM000679.2:g.63478087A>C GRCh38
NC_000017.10:g.61555448A>C , CM000679.1:g.61555448A>C GRCh37
NC_000017.9:g.58909180A>C NCBI36
NG_011648.1:g.6015A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.406A>C MANE Select ENSP00000290866.4:p.Lys136Gln
ENST00000290866.9:c.406A>C ENSP00000290866.4:p.Lys136Gln
ENST00000428043.5:c.406A>C ENSP00000397593.2:p.Lys136Gln
ENST00000579462.1:n.431A>C
ENST00000580318.1:n.595A>C
ENST00000582627.1:c.406A>C ENSP00000462280.1:p.Lys136Gln
ENST00000582678.5:c.406A>C ENSP00000462995.1:p.Lys136Gln
ENST00000583336.5:n.440A>C
ENST00000584529.5:n.440A>C
NM_000789.3:c.406A>C NP_000780.1:p.Lys136Gln
XM_005257110.1:c.-50A>C XP_005257167.1:n.-50A>C
NM_000789.4:c.406A>C MANE Select NP_000780.1:p.Lys136Gln
NM_001382700.1:c.171A>C NP_001369629.1:p.Leu57=
NM_001382701.1:c.-209A>C NP_001369630.1:n.-209A>C