Canonical Allele Identifier: CA2269943320
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483789T= , CM000679.2:g.63483789T= GRCh38
NC_000017.10:g.61561150T= , CM000679.1:g.61561150T= GRCh37
NC_000017.9:g.58914882T= NCBI36
NG_011648.1:g.11717T=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-60T= MANE Select ENSP00000290866.4:n.1587-60T=
ENST00000290866.9:c.1587-60T= ENSP00000290866.4:n.1587-60T=
ENST00000428043.5:c.1587-60T= ENSP00000397593.2:n.1587-60T=
ENST00000582678.5:c.*986-60T= ENSP00000462995.1:n.*986-60T=
NM_000789.3:c.1587-60T= NP_000780.1:n.1587-60T=
XM_005257110.1:c.1038-60T= XP_005257167.1:n.1038-60T=
NM_000789.4:c.1587-60T= MANE Select NP_000780.1:n.1587-60T=
NM_001382700.1:c.1020-60T= NP_001369629.1:n.1020-60T=
NM_001382701.1:c.735-60T= NP_001369630.1:n.735-60T=