Canonical Allele Identifier: CA985404537
Gene: ACE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63477146_63477151del , CM000679.2:g.63477146_63477151del GRCh38
NC_000017.10:g.61554507_61554512del , CM000679.1:g.61554507_61554512del GRCh37
NC_000017.9:g.58908239_58908244del NCBI36
NG_011648.1:g.5074_5079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.52_57del MANE Select ENSP00000290866.4:p.Leu18_Leu19del
ENST00000290866.9:c.52_57del ENSP00000290866.4:p.Leu18_Leu19del
ENST00000428043.5:c.52_57del ENSP00000397593.2:p.Leu18_Leu19del
ENST00000579462.1:n.77_82del
ENST00000582678.5:c.52_57del ENSP00000462995.1:p.Leu18_Leu19del
ENST00000583336.5:n.86_91del
ENST00000584529.5:n.86_91del
NM_000789.3:c.52_57del NP_000780.1:p.Leu18_Leu19del
XM_005257110.1:c.-404_-399del XP_005257167.1:n.-404_-399del
NM_000789.4:c.52_57del MANE Select NP_000780.1:p.Leu18_Leu19del
NM_001382700.1:c.-184_-179del NP_001369629.1:n.-184_-179del
NM_001382701.1:c.-563_-558del NP_001369630.1:n.-563_-558del