Canonical Allele Identifier: CA2269943310
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483777A= , CM000679.2:g.63483777A= GRCh38
NC_000017.10:g.61561138A= , CM000679.1:g.61561138A= GRCh37
NC_000017.9:g.58914870A= NCBI36
NG_011648.1:g.11705A=

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1587-72A= MANE Select ENSP00000290866.4:n.1587-72A=
ENST00000290866.9:c.1587-72A= ENSP00000290866.4:n.1587-72A=
ENST00000428043.5:c.1587-72A= ENSP00000397593.2:n.1587-72A=
ENST00000582678.5:c.*986-72A= ENSP00000462995.1:n.*986-72A=
NM_000789.3:c.1587-72A= NP_000780.1:n.1587-72A=
XM_005257110.1:c.1038-72A= XP_005257167.1:n.1038-72A=
NM_000789.4:c.1587-72A= MANE Select NP_000780.1:n.1587-72A=
NM_001382700.1:c.1020-72A= NP_001369629.1:n.1020-72A=
NM_001382701.1:c.735-72A= NP_001369630.1:n.735-72A=