Canonical Allele Identifier: CA985411674
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488677_63488688del , CM000679.2:g.63488677_63488688del GRCh38
NC_000017.10:g.61566038_61566049del , CM000679.1:g.61566038_61566049del GRCh37
NC_000017.9:g.58919770_58919781del NCBI36
NG_011648.1:g.16605_16616del

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2335_2346del MANE Select ENSP00000290866.4:p.Lys779_Asp782del
ENST00000290863.10:c.613_624del ENSP00000290863.6:p.Lys205_Asp208del
ENST00000290866.9:c.2335_2346del ENSP00000290866.4:p.Lys779_Asp782del
ENST00000413513.7:c.613_624del ENSP00000392247.3:p.Lys205_Asp208del
ENST00000428043.5:c.2335_2346del ENSP00000397593.2:p.Lys779_Asp782del
ENST00000577647.2:c.613_624del ENSP00000464149.1:p.Lys205_Asp208del
ENST00000578839.5:c.*405_*416del ENSP00000462110.2:n.*405_*416del
ENST00000579204.1:c.594_605del ENSP00000464629.1:n.594_605del
ENST00000579314.5:c.*64_*75del ENSP00000462599.1:n.*64_*75del
ENST00000582005.5:c.*255_*266del ENSP00000462002.1:n.*255_*266del
ENST00000582761.1:c.103_114del ENSP00000462909.1:p.Lys35_Asp38del
ENST00000584865.5:n.281_292del
NM_000789.3:c.2335_2346del NP_000780.1:p.Lys779_Asp782del
NM_001178057.1:c.613_624del NP_001171528.1:p.Lys205_Asp208del
NM_152830.2:c.613_624del NP_690043.1:p.Lys205_Asp208del
XM_005257110.1:c.1786_1797del XP_005257167.1:p.Lys596_Asp599del
XM_006721737.2:c.673_684del XP_006721800.2:p.Lys225_Asp228del
XM_006721737.3:c.673_684del XP_006721800.2:p.Lys225_Asp228del
NM_000789.4:c.2335_2346del MANE Select NP_000780.1:p.Lys779_Asp782del
NM_001178057.2:c.613_624del NP_001171528.1:p.Lys205_Asp208del
NM_152830.3:c.613_624del NP_690043.1:p.Lys205_Asp208del
NM_001382700.1:c.1768_1779del NP_001369629.1:p.Lys590_Asp593del
NM_001382701.1:c.1483_1494del NP_001369630.1:p.Lys495_Asp498del
NM_001382702.1:c.265_276del NP_001369631.1:p.Lys89_Asp92del
NR_168483.1:n.713_724del