Canonical Allele Identifier: CA913187317
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112827158delinsCA , CM000667.2:g.112827158delinsCA GRCh38
NC_000005.9:g.112162855delinsCA , CM000667.1:g.112162855delinsCA GRCh37
NC_000005.8:g.112190754delinsCA NCBI36
NG_008481.4:g.139638delinsCA , LRG_130:g.139638delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1408+5167delinsCA ENSP00000484935.2:n.1408+5167delinsCA
ENST00000504915.3:c.1513delinsCA ENSP00000473355.2:p.Gly505GlnfsTer4
ENST00000505084.2:n.1515delinsCA
ENST00000505350.2:c.*1465delinsCA ENSP00000481752.1:n.*1465delinsCA
ENST00000507379.6:c.1405delinsCA ENSP00000423224.2:p.Gly469GlnfsTer4
ENST00000509732.6:c.1459delinsCA ENSP00000426541.2:p.Gly487GlnfsTer4
ENST00000512211.7:c.1459delinsCA ENSP00000423828.3:p.Gly487GlnfsTer4
ENST00000257430.9:c.1459delinsCA MANE Select ENSP00000257430.4:p.Gly487GlnfsTer4
ENST00000257430.8:c.1459delinsCA ENSP00000257430.4:p.Gly487GlnfsTer4
ENST00000502371.2:c.96+5167delinsCA
ENST00000504915.2:c.148delinsCA ENSP00000473355.1:p.Gly50GlnfsTer4
ENST00000507379.5:c.1405delinsCA ENSP00000423224.1:p.Gly469GlnfsTer4
ENST00000508376.6:c.1459delinsCA ENSP00000427089.2:p.Gly487GlnfsTer4
ENST00000508624.5:c.*781delinsCA ENSP00000424265.1:n.*781delinsCA
ENST00000512211.6:c.1459delinsCA ENSP00000423828.2:p.Gly487GlnfsTer4
NM_000038.5:c.1459delinsCA NP_000029.2:p.Gly487GlnfsTer4
NM_001127510.2:c.1459delinsCA NP_001120982.1:p.Gly487GlnfsTer4
NM_001127511.2:c.1405delinsCA NP_001120983.2:p.Gly469GlnfsTer4
NM_001354895.1:c.1459delinsCA NP_001341824.1:p.Gly487GlnfsTer4
NM_001354896.1:c.1513delinsCA NP_001341825.1:p.Gly505GlnfsTer4
NM_001354897.1:c.1489delinsCA NP_001341826.1:p.Gly497GlnfsTer4
NM_001354898.1:c.1384delinsCA NP_001341827.1:p.Gly462GlnfsTer4
NM_001354899.1:c.1375delinsCA NP_001341828.1:p.Gly459GlnfsTer4
NM_001354900.1:c.1336delinsCA NP_001341829.1:p.Gly446GlnfsTer4
NM_001354901.1:c.1282delinsCA NP_001341830.1:p.Gly428GlnfsTer4
NM_001354902.1:c.1186delinsCA NP_001341831.1:p.Gly396GlnfsTer4
NM_001354903.1:c.1156delinsCA NP_001341832.1:p.Gly386GlnfsTer4
NM_001354904.1:c.1081delinsCA NP_001341833.1:p.Gly361GlnfsTer4
NM_001354905.1:c.979delinsCA NP_001341834.1:p.Gly327GlnfsTer4
NM_001354906.1:c.610delinsCA NP_001341835.1:p.Gly204GlnfsTer4
NM_000038.6:c.1459delinsCA MANE Select NP_000029.2:p.Gly487GlnfsTer4
NM_001127510.3:c.1459delinsCA NP_001120982.1:p.Gly487GlnfsTer4
NM_001127511.3:c.1405delinsCA NP_001120983.2:p.Gly469GlnfsTer4
NM_001354895.2:c.1459delinsCA NP_001341824.1:p.Gly487GlnfsTer4
NM_001354896.2:c.1513delinsCA NP_001341825.1:p.Gly505GlnfsTer4
NM_001354897.2:c.1489delinsCA NP_001341826.1:p.Gly497GlnfsTer4
NM_001354898.2:c.1384delinsCA NP_001341827.1:p.Gly462GlnfsTer4
NM_001354899.2:c.1375delinsCA NP_001341828.1:p.Gly459GlnfsTer4
NM_001354900.2:c.1336delinsCA NP_001341829.1:p.Gly446GlnfsTer4
NM_001354901.2:c.1282delinsCA NP_001341830.1:p.Gly428GlnfsTer4
NM_001354902.2:c.1186delinsCA NP_001341831.1:p.Gly396GlnfsTer4
NM_001354903.2:c.1156delinsCA NP_001341832.1:p.Gly386GlnfsTer4
NM_001354904.2:c.1081delinsCA NP_001341833.1:p.Gly361GlnfsTer4
NM_001354905.2:c.979delinsCA NP_001341834.1:p.Gly327GlnfsTer4
NM_001354906.2:c.610delinsCA NP_001341835.1:p.Gly204GlnfsTer4