Canonical Allele Identifier: CA010795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140863
dbSNP Id: rs587781330

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841530_112841533del , CM000667.2:g.112841530_112841533del GRCh38
NC_000005.9:g.112177227_112177230del , CM000667.1:g.112177227_112177230del GRCh37
NC_000005.8:g.112205126_112205129del NCBI36
NG_008481.4:g.154010_154013del , LRG_130:g.154010_154013del

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.5990_5993del ENSP00000473355.2:p.Asn1997ThrfsTer?
ENST00000505350.2:c.*5942_*5945del ENSP00000481752.1:n.*5942_*5945del
ENST00000507379.6:c.5882_5885del ENSP00000423224.2:p.Asn1961ThrfsTer?
ENST00000509732.6:c.5936_5939del ENSP00000426541.2:p.Asn1979ThrfsTer?
ENST00000512211.7:c.5936_5939del ENSP00000423828.3:p.Asn1979ThrfsTer?
ENST00000257430.9:c.5936_5939del MANE Select ENSP00000257430.4:p.Asn1979ThrfsTer?
ENST00000257430.8:c.5936_5939del ENSP00000257430.4:p.Asn1979ThrfsTer?
ENST00000508376.6:c.5936_5939del ENSP00000427089.2:p.Asn1979ThrfsTer?
ENST00000508624.5:c.*5258_*5261del ENSP00000424265.1:n.*5258_*5261del
ENST00000520401.1:c.230+12558_230+12561del
NM_000038.5:c.5936_5939del NP_000029.2:p.Asn1979ThrfsTer?
NM_001127510.2:c.5936_5939del NP_001120982.1:p.Asn1979ThrfsTer?
NM_001127511.2:c.5882_5885del NP_001120983.2:p.Asn1961ThrfsTer?
NM_001354895.1:c.5936_5939del NP_001341824.1:p.Asn1979ThrfsTer?
NM_001354896.1:c.5990_5993del NP_001341825.1:p.Asn1997ThrfsTer?
NM_001354897.1:c.5966_5969del NP_001341826.1:p.Asn1989ThrfsTer?
NM_001354898.1:c.5861_5864del NP_001341827.1:p.Asn1954ThrfsTer?
NM_001354899.1:c.5852_5855del NP_001341828.1:p.Asn1951ThrfsTer?
NM_001354900.1:c.5813_5816del NP_001341829.1:p.Asn1938ThrfsTer?
NM_001354901.1:c.5759_5762del NP_001341830.1:p.Asn1920ThrfsTer?
NM_001354902.1:c.5663_5666del NP_001341831.1:p.Asn1888ThrfsTer?
NM_001354903.1:c.5633_5636del NP_001341832.1:p.Asn1878ThrfsTer?
NM_001354904.1:c.5558_5561del NP_001341833.1:p.Asn1853ThrfsTer?
NM_001354905.1:c.5456_5459del NP_001341834.1:p.Asn1819ThrfsTer?
NM_001354906.1:c.5087_5090del NP_001341835.1:p.Asn1696ThrfsTer?
NM_000038.6:c.5936_5939del MANE Select NP_000029.2:p.Asn1979ThrfsTer?
NM_001127510.3:c.5936_5939del NP_001120982.1:p.Asn1979ThrfsTer?
NM_001127511.3:c.5882_5885del NP_001120983.2:p.Asn1961ThrfsTer?
NM_001354895.2:c.5936_5939del NP_001341824.1:p.Asn1979ThrfsTer?
NM_001354896.2:c.5990_5993del NP_001341825.1:p.Asn1997ThrfsTer?
NM_001354897.2:c.5966_5969del NP_001341826.1:p.Asn1989ThrfsTer?
NM_001354898.2:c.5861_5864del NP_001341827.1:p.Asn1954ThrfsTer?
NM_001354899.2:c.5852_5855del NP_001341828.1:p.Asn1951ThrfsTer?
NM_001354900.2:c.5813_5816del NP_001341829.1:p.Asn1938ThrfsTer?
NM_001354901.2:c.5759_5762del NP_001341830.1:p.Asn1920ThrfsTer?
NM_001354902.2:c.5663_5666del NP_001341831.1:p.Asn1888ThrfsTer?
NM_001354903.2:c.5633_5636del NP_001341832.1:p.Asn1878ThrfsTer?
NM_001354904.2:c.5558_5561del NP_001341833.1:p.Asn1853ThrfsTer?
NM_001354905.2:c.5456_5459del NP_001341834.1:p.Asn1819ThrfsTer?
NM_001354906.2:c.5087_5090del NP_001341835.1:p.Asn1696ThrfsTer?