Canonical Allele Identifier: CA2269943327
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483800T= , CM000679.2:g.63483800T= GRCh38
NC_000017.10:g.61561161T= , CM000679.1:g.61561161T= GRCh37
NC_000017.9:g.58914893T= NCBI36
NG_011648.1:g.11728T=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-49T= MANE Select ENSP00000290866.4:n.1587-49T=
ENST00000290866.9:c.1587-49T= ENSP00000290866.4:n.1587-49T=
ENST00000428043.5:c.1587-49T= ENSP00000397593.2:n.1587-49T=
ENST00000582678.5:c.*986-49T= ENSP00000462995.1:n.*986-49T=
NM_000789.3:c.1587-49T= NP_000780.1:n.1587-49T=
XM_005257110.1:c.1038-49T= XP_005257167.1:n.1038-49T=
NM_000789.4:c.1587-49T= MANE Select NP_000780.1:n.1587-49T=
NM_001382700.1:c.1020-49T= NP_001369629.1:n.1020-49T=
NM_001382701.1:c.735-49T= NP_001369630.1:n.735-49T=