Canonical Allele Identifier: CA2269939890
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477258C= , CM000679.2:g.63477258C= GRCh38
NC_000017.10:g.61554619C= , CM000679.1:g.61554619C= GRCh37
NC_000017.9:g.58908351C= NCBI36
NG_011648.1:g.5186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.164C= MANE Select ENSP00000290866.4:p.Ser55=
ENST00000290866.9:c.164C= ENSP00000290866.4:p.Ser55=
ENST00000428043.5:c.164C= ENSP00000397593.2:p.Ser55=
ENST00000579462.1:n.189C=
ENST00000582678.5:c.164C= ENSP00000462995.1:p.Ser55=
ENST00000583336.5:n.198C=
ENST00000584529.5:n.198C=
NM_000789.3:c.164C= NP_000780.1:p.Ser55=
XM_005257110.1:c.-292C= XP_005257167.1:n.-292C=
NM_000789.4:c.164C= MANE Select NP_000780.1:p.Ser55=
NM_001382700.1:c.-72C= NP_001369629.1:n.-72C=
NM_001382701.1:c.-451C= NP_001369630.1:n.-451C=