Canonical Allele Identifier: CA2695202737

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827175del , CM000667.2:g.112827175del	GRCh38
NC_000005.9:g.112162872del , CM000667.1:g.112162872del	GRCh37
NC_000005.8:g.112190771del	NCBI36
NG_008481.4:g.139655del , LRG_130:g.139655del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5184del	ENSP00000484935.2:n.1408+5184del
ENST00000504915.3:c.1530del	ENSP00000473355.2:p.Tyr511ThrfsTer5
ENST00000505084.2:n.1532del
ENST00000505350.2:c.*1482del	ENSP00000481752.1:n.*1482del
ENST00000507379.6:c.1422del	ENSP00000423224.2:p.Tyr475ThrfsTer5
ENST00000509732.6:c.1476del	ENSP00000426541.2:p.Tyr493ThrfsTer5
ENST00000512211.7:c.1476del	ENSP00000423828.3:p.Tyr493ThrfsTer5
ENST00000257430.9:c.1476del MANE Select	ENSP00000257430.4:p.Tyr493ThrfsTer5
ENST00000257430.8:c.1476del	ENSP00000257430.4:p.Tyr493ThrfsTer5
ENST00000502371.2:c.96+5184del
ENST00000504915.2:c.165del	ENSP00000473355.1:p.Tyr56ThrfsTer5
ENST00000507379.5:c.1422del	ENSP00000423224.1:p.Tyr475ThrfsTer5
ENST00000508376.6:c.1476del	ENSP00000427089.2:p.Tyr493ThrfsTer5
ENST00000508624.5:c.*798del	ENSP00000424265.1:n.*798del
ENST00000512211.6:c.1476del	ENSP00000423828.2:p.Tyr493ThrfsTer5
NM_000038.5:c.1476del	NP_000029.2:p.Tyr493ThrfsTer5
NM_001127510.2:c.1476del	NP_001120982.1:p.Tyr493ThrfsTer5
NM_001127511.2:c.1422del	NP_001120983.2:p.Tyr475ThrfsTer5
NM_001354895.1:c.1476del	NP_001341824.1:p.Tyr493ThrfsTer5
NM_001354896.1:c.1530del	NP_001341825.1:p.Tyr511ThrfsTer5
NM_001354897.1:c.1506del	NP_001341826.1:p.Tyr503ThrfsTer5
NM_001354898.1:c.1401del	NP_001341827.1:p.Tyr468ThrfsTer5
NM_001354899.1:c.1392del	NP_001341828.1:p.Tyr465ThrfsTer5
NM_001354900.1:c.1353del	NP_001341829.1:p.Tyr452ThrfsTer5
NM_001354901.1:c.1299del	NP_001341830.1:p.Tyr434ThrfsTer5
NM_001354902.1:c.1203del	NP_001341831.1:p.Tyr402ThrfsTer5
NM_001354903.1:c.1173del	NP_001341832.1:p.Tyr392ThrfsTer5
NM_001354904.1:c.1098del	NP_001341833.1:p.Tyr367ThrfsTer5
NM_001354905.1:c.996del	NP_001341834.1:p.Tyr333ThrfsTer5
NM_001354906.1:c.627del	NP_001341835.1:p.Tyr210ThrfsTer5
NM_000038.6:c.1476del MANE Select	NP_000029.2:p.Tyr493ThrfsTer5
NM_001127510.3:c.1476del	NP_001120982.1:p.Tyr493ThrfsTer5
NM_001127511.3:c.1422del	NP_001120983.2:p.Tyr475ThrfsTer5
NM_001354895.2:c.1476del	NP_001341824.1:p.Tyr493ThrfsTer5
NM_001354896.2:c.1530del	NP_001341825.1:p.Tyr511ThrfsTer5
NM_001354897.2:c.1506del	NP_001341826.1:p.Tyr503ThrfsTer5
NM_001354898.2:c.1401del	NP_001341827.1:p.Tyr468ThrfsTer5
NM_001354899.2:c.1392del	NP_001341828.1:p.Tyr465ThrfsTer5
NM_001354900.2:c.1353del	NP_001341829.1:p.Tyr452ThrfsTer5
NM_001354901.2:c.1299del	NP_001341830.1:p.Tyr434ThrfsTer5
NM_001354902.2:c.1203del	NP_001341831.1:p.Tyr402ThrfsTer5
NM_001354903.2:c.1173del	NP_001341832.1:p.Tyr392ThrfsTer5
NM_001354904.2:c.1098del	NP_001341833.1:p.Tyr367ThrfsTer5
NM_001354905.2:c.996del	NP_001341834.1:p.Tyr333ThrfsTer5
NM_001354906.2:c.627del	NP_001341835.1:p.Tyr210ThrfsTer5