Canonical Allele Identifier: CA2810114083
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477727del , CM000679.2:g.63477727del GRCh38
NC_000017.10:g.61555088del , CM000679.1:g.61555088del GRCh37
NC_000017.9:g.58908820del NCBI36
NG_011648.1:g.5655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.250-204del MANE Select ENSP00000290866.4:n.250-204del
ENST00000290866.9:c.250-204del ENSP00000290866.4:n.250-204del
ENST00000428043.5:c.250-204del ENSP00000397593.2:n.250-204del
ENST00000579462.1:n.275-204del
ENST00000580318.1:n.235del
ENST00000582627.1:c.186del ENSP00000462280.1:p.Leu63SerfsTer?
ENST00000582678.5:c.250-204del ENSP00000462995.1:n.250-204del
ENST00000583336.5:n.284-204del
ENST00000584529.5:n.284-204del
NM_000789.3:c.250-204del NP_000780.1:n.250-204del
XM_005257110.1:c.-206-204del XP_005257167.1:n.-206-204del
NM_000789.4:c.250-204del MANE Select NP_000780.1:n.250-204del
NM_001382700.1:c.15-204del NP_001369629.1:n.15-204del
NM_001382701.1:c.-365-204del NP_001369630.1:n.-365-204del