Canonical Allele Identifier: CA2269939899
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477266G= , CM000679.2:g.63477266G= GRCh38
NC_000017.10:g.61554627G= , CM000679.1:g.61554627G= GRCh37
NC_000017.9:g.58908359G= NCBI36
NG_011648.1:g.5194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.172G= MANE Select ENSP00000290866.4:p.Glu58=
ENST00000290866.9:c.172G= ENSP00000290866.4:p.Glu58=
ENST00000428043.5:c.172G= ENSP00000397593.2:p.Glu58=
ENST00000579462.1:n.197G=
ENST00000582678.5:c.172G= ENSP00000462995.1:p.Glu58=
ENST00000583336.5:n.206G=
ENST00000584529.5:n.206G=
NM_000789.3:c.172G= NP_000780.1:p.Glu58=
XM_005257110.1:c.-284G= XP_005257167.1:n.-284G=
NM_000789.4:c.172G= MANE Select NP_000780.1:p.Glu58=
NM_001382700.1:c.-64G= NP_001369629.1:n.-64G=
NM_001382701.1:c.-443G= NP_001369630.1:n.-443G=