Canonical Allele Identifier: CA645562836

Gene: APC

Linked Data

• COSMIC: COSM19202
• PubMed: PMID:20223039

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837912_112837913del , CM000667.2:g.112837912_112837913del	GRCh38
NC_000005.9:g.112173609_112173610del , CM000667.1:g.112173609_112173610del	GRCh37
NC_000005.8:g.112201508_112201509del	NCBI36
NG_008481.4:g.150392_150393del , LRG_130:g.150392_150393del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1983_1984del	ENSP00000484935.2:n.1983_1984del
ENST00000504915.3:c.2372_2373del	ENSP00000473355.2:p.Phe791Ter
ENST00000505350.2:c.*2324_*2325del	ENSP00000481752.1:n.*2324_*2325del
ENST00000507379.6:c.2264_2265del	ENSP00000423224.2:p.Phe755Ter
ENST00000509732.6:c.2318_2319del	ENSP00000426541.2:p.Phe773Ter
ENST00000512211.7:c.2318_2319del	ENSP00000423828.3:p.Phe773Ter
ENST00000257430.9:c.2318_2319del MANE Select	ENSP00000257430.4:p.Phe773Ter
ENST00000257430.8:c.2318_2319del	ENSP00000257430.4:p.Phe773Ter
ENST00000502371.2:c.671_672del
ENST00000507379.5:c.2264_2265del	ENSP00000423224.1:p.Phe755Ter
ENST00000508376.6:c.2318_2319del	ENSP00000427089.2:p.Phe773Ter
ENST00000508624.5:c.*1640_*1641del	ENSP00000424265.1:n.*1640_*1641del
ENST00000512211.6:c.2318_2319del	ENSP00000423828.2:p.Phe773Ter
ENST00000520401.1:c.230+8940_230+8941del
NM_000038.5:c.2318_2319del	NP_000029.2:p.Phe773Ter
NM_001127510.2:c.2318_2319del	NP_001120982.1:p.Phe773Ter
NM_001127511.2:c.2264_2265del	NP_001120983.2:p.Phe755Ter
NM_001354895.1:c.2318_2319del	NP_001341824.1:p.Phe773Ter
NM_001354896.1:c.2372_2373del	NP_001341825.1:p.Phe791Ter
NM_001354897.1:c.2348_2349del	NP_001341826.1:p.Phe783Ter
NM_001354898.1:c.2243_2244del	NP_001341827.1:p.Phe748Ter
NM_001354899.1:c.2234_2235del	NP_001341828.1:p.Phe745Ter
NM_001354900.1:c.2195_2196del	NP_001341829.1:p.Phe732Ter
NM_001354901.1:c.2141_2142del	NP_001341830.1:p.Phe714Ter
NM_001354902.1:c.2045_2046del	NP_001341831.1:p.Phe682Ter
NM_001354903.1:c.2015_2016del	NP_001341832.1:p.Phe672Ter
NM_001354904.1:c.1940_1941del	NP_001341833.1:p.Phe647Ter
NM_001354905.1:c.1838_1839del	NP_001341834.1:p.Phe613Ter
NM_001354906.1:c.1469_1470del	NP_001341835.1:p.Phe490Ter
NM_000038.6:c.2318_2319del MANE Select	NP_000029.2:p.Phe773Ter
NM_001127510.3:c.2318_2319del	NP_001120982.1:p.Phe773Ter
NM_001127511.3:c.2264_2265del	NP_001120983.2:p.Phe755Ter
NM_001354895.2:c.2318_2319del	NP_001341824.1:p.Phe773Ter
NM_001354896.2:c.2372_2373del	NP_001341825.1:p.Phe791Ter
NM_001354897.2:c.2348_2349del	NP_001341826.1:p.Phe783Ter
NM_001354898.2:c.2243_2244del	NP_001341827.1:p.Phe748Ter
NM_001354899.2:c.2234_2235del	NP_001341828.1:p.Phe745Ter
NM_001354900.2:c.2195_2196del	NP_001341829.1:p.Phe732Ter
NM_001354901.2:c.2141_2142del	NP_001341830.1:p.Phe714Ter
NM_001354902.2:c.2045_2046del	NP_001341831.1:p.Phe682Ter
NM_001354903.2:c.2015_2016del	NP_001341832.1:p.Phe672Ter
NM_001354904.2:c.1940_1941del	NP_001341833.1:p.Phe647Ter
NM_001354905.2:c.1838_1839del	NP_001341834.1:p.Phe613Ter
NM_001354906.2:c.1469_1470del	NP_001341835.1:p.Phe490Ter