Canonical Allele Identifier: CA658760451

Gene: APC

Linked Data

• PubMed: PMID:10083733

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827160del , CM000667.2:g.112827160del	GRCh38
NC_000005.9:g.112162857del , CM000667.1:g.112162857del	GRCh37
NC_000005.8:g.112190756del	NCBI36
NG_008481.4:g.139640del , LRG_130:g.139640del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5169del	ENSP00000484935.2:n.1408+5169del
ENST00000504915.3:c.1515del	ENSP00000473355.2:p.Thr507LeufsTer9
ENST00000505084.2:n.1517del
ENST00000505350.2:c.*1467del	ENSP00000481752.1:n.*1467del
ENST00000507379.6:c.1407del	ENSP00000423224.2:p.Thr471LeufsTer9
ENST00000509732.6:c.1461del	ENSP00000426541.2:p.Thr489LeufsTer9
ENST00000512211.7:c.1461del	ENSP00000423828.3:p.Thr489LeufsTer9
ENST00000257430.9:c.1461del MANE Select	ENSP00000257430.4:p.Thr489LeufsTer9
ENST00000257430.8:c.1461del	ENSP00000257430.4:p.Thr489LeufsTer9
ENST00000502371.2:c.96+5169del
ENST00000504915.2:c.150del	ENSP00000473355.1:p.Thr52LeufsTer9
ENST00000507379.5:c.1407del	ENSP00000423224.1:p.Thr471LeufsTer9
ENST00000508376.6:c.1461del	ENSP00000427089.2:p.Thr489LeufsTer9
ENST00000508624.5:c.*783del	ENSP00000424265.1:n.*783del
ENST00000512211.6:c.1461del	ENSP00000423828.2:p.Thr489LeufsTer9
NM_000038.5:c.1461del	NP_000029.2:p.Thr489LeufsTer9
NM_001127510.2:c.1461del	NP_001120982.1:p.Thr489LeufsTer9
NM_001127511.2:c.1407del	NP_001120983.2:p.Thr471LeufsTer9
NM_001354895.1:c.1461del	NP_001341824.1:p.Thr489LeufsTer9
NM_001354896.1:c.1515del	NP_001341825.1:p.Thr507LeufsTer9
NM_001354897.1:c.1491del	NP_001341826.1:p.Thr499LeufsTer9
NM_001354898.1:c.1386del	NP_001341827.1:p.Thr464LeufsTer9
NM_001354899.1:c.1377del	NP_001341828.1:p.Thr461LeufsTer9
NM_001354900.1:c.1338del	NP_001341829.1:p.Thr448LeufsTer9
NM_001354901.1:c.1284del	NP_001341830.1:p.Thr430LeufsTer9
NM_001354902.1:c.1188del	NP_001341831.1:p.Thr398LeufsTer9
NM_001354903.1:c.1158del	NP_001341832.1:p.Thr388LeufsTer9
NM_001354904.1:c.1083del	NP_001341833.1:p.Thr363LeufsTer9
NM_001354905.1:c.981del	NP_001341834.1:p.Thr329LeufsTer9
NM_001354906.1:c.612del	NP_001341835.1:p.Thr206LeufsTer9
NM_000038.6:c.1461del MANE Select	NP_000029.2:p.Thr489LeufsTer9
NM_001127510.3:c.1461del	NP_001120982.1:p.Thr489LeufsTer9
NM_001127511.3:c.1407del	NP_001120983.2:p.Thr471LeufsTer9
NM_001354895.2:c.1461del	NP_001341824.1:p.Thr489LeufsTer9
NM_001354896.2:c.1515del	NP_001341825.1:p.Thr507LeufsTer9
NM_001354897.2:c.1491del	NP_001341826.1:p.Thr499LeufsTer9
NM_001354898.2:c.1386del	NP_001341827.1:p.Thr464LeufsTer9
NM_001354899.2:c.1377del	NP_001341828.1:p.Thr461LeufsTer9
NM_001354900.2:c.1338del	NP_001341829.1:p.Thr448LeufsTer9
NM_001354901.2:c.1284del	NP_001341830.1:p.Thr430LeufsTer9
NM_001354902.2:c.1188del	NP_001341831.1:p.Thr398LeufsTer9
NM_001354903.2:c.1158del	NP_001341832.1:p.Thr388LeufsTer9
NM_001354904.2:c.1083del	NP_001341833.1:p.Thr363LeufsTer9
NM_001354905.2:c.981del	NP_001341834.1:p.Thr329LeufsTer9
NM_001354906.2:c.612del	NP_001341835.1:p.Thr206LeufsTer9