Canonical Allele Identifier: CA658760453

Gene: APC

Linked Data

• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827163dup , CM000667.2:g.112827163dup	GRCh38
NC_000005.9:g.112162860dup , CM000667.1:g.112162860dup	GRCh37
NC_000005.8:g.112190759dup	NCBI36
NG_008481.4:g.139643dup , LRG_130:g.139643dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5172dup	ENSP00000484935.2:n.1408+5172dup
ENST00000504915.3:c.1518dup	ENSP00000473355.2:p.Thr507TyrfsTer2
ENST00000505084.2:n.1520dup
ENST00000505350.2:c.*1470dup	ENSP00000481752.1:n.*1470dup
ENST00000507379.6:c.1410dup	ENSP00000423224.2:p.Thr471TyrfsTer2
ENST00000509732.6:c.1464dup	ENSP00000426541.2:p.Thr489TyrfsTer2
ENST00000512211.7:c.1464dup	ENSP00000423828.3:p.Thr489TyrfsTer2
ENST00000257430.9:c.1464dup MANE Select	ENSP00000257430.4:p.Thr489TyrfsTer2
ENST00000257430.8:c.1464dup	ENSP00000257430.4:p.Thr489TyrfsTer2
ENST00000502371.2:c.96+5172dup
ENST00000504915.2:c.153dup	ENSP00000473355.1:p.Thr52TyrfsTer2
ENST00000507379.5:c.1410dup	ENSP00000423224.1:p.Thr471TyrfsTer2
ENST00000508376.6:c.1464dup	ENSP00000427089.2:p.Thr489TyrfsTer2
ENST00000508624.5:c.*786dup	ENSP00000424265.1:n.*786dup
ENST00000512211.6:c.1464dup	ENSP00000423828.2:p.Thr489TyrfsTer2
NM_000038.5:c.1464dup	NP_000029.2:p.Thr489TyrfsTer2
NM_001127510.2:c.1464dup	NP_001120982.1:p.Thr489TyrfsTer2
NM_001127511.2:c.1410dup	NP_001120983.2:p.Thr471TyrfsTer2
NM_001354895.1:c.1464dup	NP_001341824.1:p.Thr489TyrfsTer2
NM_001354896.1:c.1518dup	NP_001341825.1:p.Thr507TyrfsTer2
NM_001354897.1:c.1494dup	NP_001341826.1:p.Thr499TyrfsTer2
NM_001354898.1:c.1389dup	NP_001341827.1:p.Thr464TyrfsTer2
NM_001354899.1:c.1380dup	NP_001341828.1:p.Thr461TyrfsTer2
NM_001354900.1:c.1341dup	NP_001341829.1:p.Thr448TyrfsTer2
NM_001354901.1:c.1287dup	NP_001341830.1:p.Thr430TyrfsTer2
NM_001354902.1:c.1191dup	NP_001341831.1:p.Thr398TyrfsTer2
NM_001354903.1:c.1161dup	NP_001341832.1:p.Thr388TyrfsTer2
NM_001354904.1:c.1086dup	NP_001341833.1:p.Thr363TyrfsTer2
NM_001354905.1:c.984dup	NP_001341834.1:p.Thr329TyrfsTer2
NM_001354906.1:c.615dup	NP_001341835.1:p.Thr206TyrfsTer2
NM_000038.6:c.1464dup MANE Select	NP_000029.2:p.Thr489TyrfsTer2
NM_001127510.3:c.1464dup	NP_001120982.1:p.Thr489TyrfsTer2
NM_001127511.3:c.1410dup	NP_001120983.2:p.Thr471TyrfsTer2
NM_001354895.2:c.1464dup	NP_001341824.1:p.Thr489TyrfsTer2
NM_001354896.2:c.1518dup	NP_001341825.1:p.Thr507TyrfsTer2
NM_001354897.2:c.1494dup	NP_001341826.1:p.Thr499TyrfsTer2
NM_001354898.2:c.1389dup	NP_001341827.1:p.Thr464TyrfsTer2
NM_001354899.2:c.1380dup	NP_001341828.1:p.Thr461TyrfsTer2
NM_001354900.2:c.1341dup	NP_001341829.1:p.Thr448TyrfsTer2
NM_001354901.2:c.1287dup	NP_001341830.1:p.Thr430TyrfsTer2
NM_001354902.2:c.1191dup	NP_001341831.1:p.Thr398TyrfsTer2
NM_001354903.2:c.1161dup	NP_001341832.1:p.Thr388TyrfsTer2
NM_001354904.2:c.1086dup	NP_001341833.1:p.Thr363TyrfsTer2
NM_001354905.2:c.984dup	NP_001341834.1:p.Thr329TyrfsTer2
NM_001354906.2:c.615dup	NP_001341835.1:p.Thr206TyrfsTer2