Canonical Allele Identifier: CA985411336
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63488529_63488530insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG , CM000679.2:g.63488529_63488530insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG GRCh38
NC_000017.10:g.61565890_61565891insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG , CM000679.1:g.61565890_61565891insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG GRCh37
NC_000017.9:g.58919622_58919623insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NCBI36
NG_011648.1:g.16457_16458insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.2306-119_2306-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG MANE Select ENSP00000290866.4:n.2306-119_2306-118insG...
ENST00000290863.10:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000290863.6:n.584-119_584-118insGAC...
ENST00000290866.9:c.2306-119_2306-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000290866.4:n.2306-119_2306-118insG...
ENST00000413513.7:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000392247.3:n.584-119_584-118insGAC...
ENST00000428043.5:c.2306-119_2306-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000397593.2:n.2306-119_2306-118insG...
ENST00000577647.2:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000464149.1:n.584-119_584-118insGAC...
ENST00000578839.5:c.*376-119_*376-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000462110.2:n.*376-119_*376-118insG...
ENST00000579204.1:c.487-41_487-40insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000464629.1:n.487-41_487-40insGACCT...
ENST00000579314.5:c.584-41_584-40insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000462599.1:n.584-41_584-40insGACCT...
ENST00000582005.5:c.*226-119_*226-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000462002.1:n.*226-119_*226-118insG...
ENST00000582761.1:c.74-119_74-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG ENSP00000462909.1:n.74-119_74-118insGACCT...
ENST00000584865.5:n.252-119_252-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG
NM_000789.3:c.2306-119_2306-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_000780.1:n.2306-119_2306-118insGACCTCG...
NM_001178057.1:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_001171528.1:n.584-119_584-118insGACCTC...
NM_152830.2:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_690043.1:n.584-119_584-118insGACCTCGTG...
XM_005257110.1:c.1757-119_1757-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG XP_005257167.1:n.1757-119_1757-118insGACC...
XM_006721737.2:c.644-119_644-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG XP_006721800.2:n.644-119_644-118insGACCTC...
XM_006721737.3:c.644-119_644-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG XP_006721800.2:n.644-119_644-118insGACCTC...
NM_000789.4:c.2306-119_2306-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG MANE Select NP_000780.1:n.2306-119_2306-118insGACCTCG...
NM_001178057.2:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_001171528.1:n.584-119_584-118insGACCTC...
NM_152830.3:c.584-119_584-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_690043.1:n.584-119_584-118insGACCTCGTG...
NM_001382700.1:c.1739-119_1739-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_001369629.1:n.1739-119_1739-118insGACC...
NM_001382701.1:c.1454-119_1454-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_001369630.1:n.1454-119_1454-118insGACC...
NM_001382702.1:c.236-119_236-118insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG NP_001369631.1:n.236-119_236-118insGACCTC...
NR_168483.1:n.606-41_606-40insGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTG