Canonical Allele Identifier: CA645543642

Gene: APC

Linked Data

• COSMIC: COSM26696

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839499_112839503del , CM000667.2:g.112839499_112839503del	GRCh38
NC_000005.9:g.112175196_112175200del , CM000667.1:g.112175196_112175200del	GRCh37
NC_000005.8:g.112203095_112203099del	NCBI36
NG_008481.4:g.151979_151983del , LRG_130:g.151979_151983del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3570_3574del	ENSP00000484935.2:n.3570_3574del
ENST00000504915.3:c.3959_3963del	ENSP00000473355.2:p.Leu1320HisfsTer11
ENST00000505350.2:c.*3911_*3915del	ENSP00000481752.1:n.*3911_*3915del
ENST00000507379.6:c.3851_3855del	ENSP00000423224.2:p.Leu1284HisfsTer11
ENST00000509732.6:c.3905_3909del	ENSP00000426541.2:p.Leu1302HisfsTer11
ENST00000512211.7:c.3905_3909del	ENSP00000423828.3:p.Leu1302HisfsTer11
ENST00000257430.9:c.3905_3909del MANE Select	ENSP00000257430.4:p.Leu1302HisfsTer11
ENST00000257430.8:c.3905_3909del	ENSP00000257430.4:p.Leu1302HisfsTer11
ENST00000502371.2:c.2258_2262del
ENST00000508376.6:c.3905_3909del	ENSP00000427089.2:p.Leu1302HisfsTer11
ENST00000508624.5:c.*3227_*3231del	ENSP00000424265.1:n.*3227_*3231del
ENST00000512211.6:c.3905_3909del	ENSP00000423828.2:p.Leu1302HisfsTer?
ENST00000520401.1:c.230+10527_230+10531del
NM_000038.5:c.3905_3909del	NP_000029.2:p.Leu1302HisfsTer11
NM_001127510.2:c.3905_3909del	NP_001120982.1:p.Leu1302HisfsTer11
NM_001127511.2:c.3851_3855del	NP_001120983.2:p.Leu1284HisfsTer11
NM_001354895.1:c.3905_3909del	NP_001341824.1:p.Leu1302HisfsTer11
NM_001354896.1:c.3959_3963del	NP_001341825.1:p.Leu1320HisfsTer11
NM_001354897.1:c.3935_3939del	NP_001341826.1:p.Leu1312HisfsTer11
NM_001354898.1:c.3830_3834del	NP_001341827.1:p.Leu1277HisfsTer11
NM_001354899.1:c.3821_3825del	NP_001341828.1:p.Leu1274HisfsTer11
NM_001354900.1:c.3782_3786del	NP_001341829.1:p.Leu1261HisfsTer11
NM_001354901.1:c.3728_3732del	NP_001341830.1:p.Leu1243HisfsTer11
NM_001354902.1:c.3632_3636del	NP_001341831.1:p.Leu1211HisfsTer11
NM_001354903.1:c.3602_3606del	NP_001341832.1:p.Leu1201HisfsTer11
NM_001354904.1:c.3527_3531del	NP_001341833.1:p.Leu1176HisfsTer11
NM_001354905.1:c.3425_3429del	NP_001341834.1:p.Leu1142HisfsTer11
NM_001354906.1:c.3056_3060del	NP_001341835.1:p.Leu1019HisfsTer11
NM_000038.6:c.3905_3909del MANE Select	NP_000029.2:p.Leu1302HisfsTer11
NM_001127510.3:c.3905_3909del	NP_001120982.1:p.Leu1302HisfsTer11
NM_001127511.3:c.3851_3855del	NP_001120983.2:p.Leu1284HisfsTer11
NM_001354895.2:c.3905_3909del	NP_001341824.1:p.Leu1302HisfsTer11
NM_001354896.2:c.3959_3963del	NP_001341825.1:p.Leu1320HisfsTer11
NM_001354897.2:c.3935_3939del	NP_001341826.1:p.Leu1312HisfsTer11
NM_001354898.2:c.3830_3834del	NP_001341827.1:p.Leu1277HisfsTer11
NM_001354899.2:c.3821_3825del	NP_001341828.1:p.Leu1274HisfsTer11
NM_001354900.2:c.3782_3786del	NP_001341829.1:p.Leu1261HisfsTer11
NM_001354901.2:c.3728_3732del	NP_001341830.1:p.Leu1243HisfsTer11
NM_001354902.2:c.3632_3636del	NP_001341831.1:p.Leu1211HisfsTer11
NM_001354903.2:c.3602_3606del	NP_001341832.1:p.Leu1201HisfsTer11
NM_001354904.2:c.3527_3531del	NP_001341833.1:p.Leu1176HisfsTer11
NM_001354905.2:c.3425_3429del	NP_001341834.1:p.Leu1142HisfsTer11
NM_001354906.2:c.3056_3060del	NP_001341835.1:p.Leu1019HisfsTer11