Canonical Allele Identifier: CA645562789

Gene: APC

Linked Data

• COSMIC: COSM3773394

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827170_112827177dup , CM000667.2:g.112827170_112827177dup	GRCh38
NC_000005.9:g.112162867_112162874dup , CM000667.1:g.112162867_112162874dup	GRCh37
NC_000005.8:g.112190766_112190773dup	NCBI36
NG_008481.4:g.139650_139657dup , LRG_130:g.139650_139657dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5179_1408+5186dup	ENSP00000484935.2:n.1408+5179_1408+5186du...
ENST00000504915.3:c.1525_1532dup	ENSP00000473355.2:p.Tyr511Ter
ENST00000505084.2:n.1527_1534dup
ENST00000505350.2:c.*1477_*1484dup	ENSP00000481752.1:n.*1477_*1484dup
ENST00000507379.6:c.1417_1424dup	ENSP00000423224.2:p.Tyr475Ter
ENST00000509732.6:c.1471_1478dup	ENSP00000426541.2:p.Tyr493Ter
ENST00000512211.7:c.1471_1478dup	ENSP00000423828.3:p.Tyr493Ter
ENST00000257430.9:c.1471_1478dup MANE Select	ENSP00000257430.4:p.Tyr493Ter
ENST00000257430.8:c.1471_1478dup	ENSP00000257430.4:p.Tyr493Ter
ENST00000502371.2:c.96+5179_96+5186dup
ENST00000504915.2:c.160_167dup	ENSP00000473355.1:p.Tyr56Ter
ENST00000507379.5:c.1417_1424dup	ENSP00000423224.1:p.Tyr475Ter
ENST00000508376.6:c.1471_1478dup	ENSP00000427089.2:p.Tyr493Ter
ENST00000508624.5:c.*793_*800dup	ENSP00000424265.1:n.*793_*800dup
ENST00000512211.6:c.1471_1478dup	ENSP00000423828.2:p.Tyr493Ter
NM_000038.5:c.1471_1478dup	NP_000029.2:p.Tyr493Ter
NM_001127510.2:c.1471_1478dup	NP_001120982.1:p.Tyr493Ter
NM_001127511.2:c.1417_1424dup	NP_001120983.2:p.Tyr475Ter
NM_001354895.1:c.1471_1478dup	NP_001341824.1:p.Tyr493Ter
NM_001354896.1:c.1525_1532dup	NP_001341825.1:p.Tyr511Ter
NM_001354897.1:c.1501_1508dup	NP_001341826.1:p.Tyr503Ter
NM_001354898.1:c.1396_1403dup	NP_001341827.1:p.Tyr468Ter
NM_001354899.1:c.1387_1394dup	NP_001341828.1:p.Tyr465Ter
NM_001354900.1:c.1348_1355dup	NP_001341829.1:p.Tyr452Ter
NM_001354901.1:c.1294_1301dup	NP_001341830.1:p.Tyr434Ter
NM_001354902.1:c.1198_1205dup	NP_001341831.1:p.Tyr402Ter
NM_001354903.1:c.1168_1175dup	NP_001341832.1:p.Tyr392Ter
NM_001354904.1:c.1093_1100dup	NP_001341833.1:p.Tyr367Ter
NM_001354905.1:c.991_998dup	NP_001341834.1:p.Tyr333Ter
NM_001354906.1:c.622_629dup	NP_001341835.1:p.Tyr210Ter
NM_000038.6:c.1471_1478dup MANE Select	NP_000029.2:p.Tyr493Ter
NM_001127510.3:c.1471_1478dup	NP_001120982.1:p.Tyr493Ter
NM_001127511.3:c.1417_1424dup	NP_001120983.2:p.Tyr475Ter
NM_001354895.2:c.1471_1478dup	NP_001341824.1:p.Tyr493Ter
NM_001354896.2:c.1525_1532dup	NP_001341825.1:p.Tyr511Ter
NM_001354897.2:c.1501_1508dup	NP_001341826.1:p.Tyr503Ter
NM_001354898.2:c.1396_1403dup	NP_001341827.1:p.Tyr468Ter
NM_001354899.2:c.1387_1394dup	NP_001341828.1:p.Tyr465Ter
NM_001354900.2:c.1348_1355dup	NP_001341829.1:p.Tyr452Ter
NM_001354901.2:c.1294_1301dup	NP_001341830.1:p.Tyr434Ter
NM_001354902.2:c.1198_1205dup	NP_001341831.1:p.Tyr402Ter
NM_001354903.2:c.1168_1175dup	NP_001341832.1:p.Tyr392Ter
NM_001354904.2:c.1093_1100dup	NP_001341833.1:p.Tyr367Ter
NM_001354905.2:c.991_998dup	NP_001341834.1:p.Tyr333Ter
NM_001354906.2:c.622_629dup	NP_001341835.1:p.Tyr210Ter