Canonical Allele Identifier: CA2269950688
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498376G= , CM000679.2:g.63498376G= GRCh38
NC_000017.10:g.61575737G= , CM000679.1:g.61575737G= GRCh37
NC_000017.9:g.58929469G= NCBI36
NG_011648.1:g.26304G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.9:c.*1010G= ENSP00000290866.4:n.*1010G=
ENST00000428043.5:c.*1353G= ENSP00000397593.2:n.*1353G=
ENST00000577647.2:c.1969+1391G= ENSP00000464149.1:n.1969+1391G=
NM_000789.3:c.*1010G= NP_000780.1:n.*1010G=
NM_001178057.1:c.*1010G= NP_001171528.1:n.*1010G=
NM_152830.2:c.*1010G= NP_690043.1:n.*1010G=
XM_005257110.1:c.*1010G= XP_005257167.1:n.*1010G=
XM_006721737.2:c.*1010G= XP_006721800.2:n.*1010G=