Canonical Allele Identifier: CA006371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 42240
dbSNP Id: rs397515732

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112835124dup , CM000667.2:g.112835124dup GRCh38
NC_000005.9:g.112170821dup , CM000667.1:g.112170821dup GRCh37
NC_000005.8:g.112198720dup NCBI36
NG_008481.4:g.147604dup , LRG_130:g.147604dup

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1582dup ENSP00000484935.2:n.1582dup
ENST00000504915.3:c.1971dup ENSP00000473355.2:p.Arg658ThrfsTer11
ENST00000505350.2:c.*1923dup ENSP00000481752.1:n.*1923dup
ENST00000507379.6:c.1863dup ENSP00000423224.2:p.Arg622ThrfsTer11
ENST00000509732.6:c.1917dup ENSP00000426541.2:p.Arg640ThrfsTer11
ENST00000512211.7:c.1917dup ENSP00000423828.3:p.Arg640ThrfsTer11
ENST00000257430.9:c.1917dup MANE Select ENSP00000257430.4:p.Arg640ThrfsTer11
ENST00000257430.8:c.1917dup ENSP00000257430.4:p.Arg640ThrfsTer11
ENST00000502371.2:c.270dup
ENST00000504915.2:c.606dup ENSP00000473355.1:p.Arg203ThrfsTer11
ENST00000507379.5:c.1863dup ENSP00000423224.1:p.Arg622ThrfsTer11
ENST00000508376.6:c.1917dup ENSP00000427089.2:p.Arg640ThrfsTer11
ENST00000508624.5:c.*1239dup ENSP00000424265.1:n.*1239dup
ENST00000512211.6:c.1917dup ENSP00000423828.2:p.Arg640ThrfsTer11
ENST00000520401.1:c.230+6152dup
NM_000038.5:c.1917dup NP_000029.2:p.Arg640ThrfsTer11
NM_001127510.2:c.1917dup NP_001120982.1:p.Arg640ThrfsTer11
NM_001127511.2:c.1863dup NP_001120983.2:p.Arg622ThrfsTer11
NM_001354895.1:c.1917dup NP_001341824.1:p.Arg640ThrfsTer11
NM_001354896.1:c.1971dup NP_001341825.1:p.Arg658ThrfsTer11
NM_001354897.1:c.1947dup NP_001341826.1:p.Arg650ThrfsTer11
NM_001354898.1:c.1842dup NP_001341827.1:p.Arg615ThrfsTer11
NM_001354899.1:c.1833dup NP_001341828.1:p.Arg612ThrfsTer11
NM_001354900.1:c.1794dup NP_001341829.1:p.Arg599ThrfsTer11
NM_001354901.1:c.1740dup NP_001341830.1:p.Arg581ThrfsTer11
NM_001354902.1:c.1644dup NP_001341831.1:p.Arg549ThrfsTer11
NM_001354903.1:c.1614dup NP_001341832.1:p.Arg539ThrfsTer11
NM_001354904.1:c.1539dup NP_001341833.1:p.Arg514ThrfsTer11
NM_001354905.1:c.1437dup NP_001341834.1:p.Arg480ThrfsTer11
NM_001354906.1:c.1068dup NP_001341835.1:p.Arg357ThrfsTer11
NM_000038.6:c.1917dup MANE Select NP_000029.2:p.Arg640ThrfsTer11
NM_001127510.3:c.1917dup NP_001120982.1:p.Arg640ThrfsTer11
NM_001127511.3:c.1863dup NP_001120983.2:p.Arg622ThrfsTer11
NM_001354895.2:c.1917dup NP_001341824.1:p.Arg640ThrfsTer11
NM_001354896.2:c.1971dup NP_001341825.1:p.Arg658ThrfsTer11
NM_001354897.2:c.1947dup NP_001341826.1:p.Arg650ThrfsTer11
NM_001354898.2:c.1842dup NP_001341827.1:p.Arg615ThrfsTer11
NM_001354899.2:c.1833dup NP_001341828.1:p.Arg612ThrfsTer11
NM_001354900.2:c.1794dup NP_001341829.1:p.Arg599ThrfsTer11
NM_001354901.2:c.1740dup NP_001341830.1:p.Arg581ThrfsTer11
NM_001354902.2:c.1644dup NP_001341831.1:p.Arg549ThrfsTer11
NM_001354903.2:c.1614dup NP_001341832.1:p.Arg539ThrfsTer11
NM_001354904.2:c.1539dup NP_001341833.1:p.Arg514ThrfsTer11
NM_001354905.2:c.1437dup NP_001341834.1:p.Arg480ThrfsTer11
NM_001354906.2:c.1068dup NP_001341835.1:p.Arg357ThrfsTer11