Canonical Allele Identifier: CA2269943110
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483420A= , CM000679.2:g.63483420A= GRCh38
NC_000017.10:g.61560781A= , CM000679.1:g.61560781A= GRCh37
NC_000017.9:g.58914513A= NCBI36
NG_011648.1:g.11348A=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1488-40A= MANE Select ENSP00000290866.4:n.1488-40A=
ENST00000290866.9:c.1488-40A= ENSP00000290866.4:n.1488-40A=
ENST00000428043.5:c.1488-40A= ENSP00000397593.2:n.1488-40A=
ENST00000582678.5:c.*887-40A= ENSP00000462995.1:n.*887-40A=
ENST00000584529.5:n.1377-40A=
NM_000789.3:c.1488-40A= NP_000780.1:n.1488-40A=
XM_005257110.1:c.939-40A= XP_005257167.1:n.939-40A=
NM_000789.4:c.1488-40A= MANE Select NP_000780.1:n.1488-40A=
NM_001382700.1:c.921-40A= NP_001369629.1:n.921-40A=
NM_001382701.1:c.636-40A= NP_001369630.1:n.636-40A=