Canonical Allele Identifier: CA011093
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs587780602
COSMIC: COSM48919

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841957_112841959dup , CM000667.2:g.112841957_112841959dup GRCh38
NC_000005.9:g.112177654_112177656dup , CM000667.1:g.112177654_112177656dup GRCh37
NC_000005.8:g.112205553_112205555dup NCBI36
NG_008481.4:g.154437_154439dup , LRG_130:g.154437_154439dup

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.6417_6419dup ENSP00000473355.2:p.Ala2140_Cys2141insAla...
ENST00000505350.2:c.*6369_*6371dup ENSP00000481752.1:n.*6369_*6371dup
ENST00000507379.6:c.6309_6311dup ENSP00000423224.2:p.Ala2104_Cys2105insAla...
ENST00000509732.6:c.6363_6365dup ENSP00000426541.2:p.Ala2122_Cys2123insAla...
ENST00000512211.7:c.6363_6365dup ENSP00000423828.3:p.Ala2122_Cys2123insAla...
ENST00000257430.9:c.6363_6365dup MANE Select ENSP00000257430.4:p.Ala2122_Cys2123insAla...
ENST00000257430.8:c.6363_6365dup ENSP00000257430.4:p.Ala2122_Cys2123insAla...
ENST00000508376.6:c.6363_6365dup ENSP00000427089.2:p.Ala2122_Cys2123insAla...
ENST00000508624.5:c.*5685_*5687dup ENSP00000424265.1:n.*5685_*5687dup
ENST00000520401.1:c.230+12985_230+12987dup
NM_000038.5:c.6363_6365dup NP_000029.2:p.Ala2122_Cys2123insAla
NM_001127510.2:c.6363_6365dup NP_001120982.1:p.Ala2122_Cys2123insAla
NM_001127511.2:c.6309_6311dup NP_001120983.2:p.Ala2104_Cys2105insAla
NM_001354895.1:c.6363_6365dup NP_001341824.1:p.Ala2122_Cys2123insAla
NM_001354896.1:c.6417_6419dup NP_001341825.1:p.Ala2140_Cys2141insAla
NM_001354897.1:c.6393_6395dup NP_001341826.1:p.Ala2132_Cys2133insAla
NM_001354898.1:c.6288_6290dup NP_001341827.1:p.Ala2097_Cys2098insAla
NM_001354899.1:c.6279_6281dup NP_001341828.1:p.Ala2094_Cys2095insAla
NM_001354900.1:c.6240_6242dup NP_001341829.1:p.Ala2081_Cys2082insAla
NM_001354901.1:c.6186_6188dup NP_001341830.1:p.Ala2063_Cys2064insAla
NM_001354902.1:c.6090_6092dup NP_001341831.1:p.Ala2031_Cys2032insAla
NM_001354903.1:c.6060_6062dup NP_001341832.1:p.Ala2021_Cys2022insAla
NM_001354904.1:c.5985_5987dup NP_001341833.1:p.Ala1996_Cys1997insAla
NM_001354905.1:c.5883_5885dup NP_001341834.1:p.Ala1962_Cys1963insAla
NM_001354906.1:c.5514_5516dup NP_001341835.1:p.Ala1839_Cys1840insAla
NM_000038.6:c.6363_6365dup MANE Select NP_000029.2:p.Ala2122_Cys2123insAla
NM_001127510.3:c.6363_6365dup NP_001120982.1:p.Ala2122_Cys2123insAla
NM_001127511.3:c.6309_6311dup NP_001120983.2:p.Ala2104_Cys2105insAla
NM_001354895.2:c.6363_6365dup NP_001341824.1:p.Ala2122_Cys2123insAla
NM_001354896.2:c.6417_6419dup NP_001341825.1:p.Ala2140_Cys2141insAla
NM_001354897.2:c.6393_6395dup NP_001341826.1:p.Ala2132_Cys2133insAla
NM_001354898.2:c.6288_6290dup NP_001341827.1:p.Ala2097_Cys2098insAla
NM_001354899.2:c.6279_6281dup NP_001341828.1:p.Ala2094_Cys2095insAla
NM_001354900.2:c.6240_6242dup NP_001341829.1:p.Ala2081_Cys2082insAla
NM_001354901.2:c.6186_6188dup NP_001341830.1:p.Ala2063_Cys2064insAla
NM_001354902.2:c.6090_6092dup NP_001341831.1:p.Ala2031_Cys2032insAla
NM_001354903.2:c.6060_6062dup NP_001341832.1:p.Ala2021_Cys2022insAla
NM_001354904.2:c.5985_5987dup NP_001341833.1:p.Ala1996_Cys1997insAla
NM_001354905.2:c.5883_5885dup NP_001341834.1:p.Ala1962_Cys1963insAla
NM_001354906.2:c.5514_5516dup NP_001341835.1:p.Ala1839_Cys1840insAla