Canonical Allele Identifier: CA658760866

Gene: APC

Linked Data

• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838650dup , CM000667.2:g.112838650dup	GRCh38
NC_000005.9:g.112174347dup , CM000667.1:g.112174347dup	GRCh37
NC_000005.8:g.112202246dup	NCBI36
NG_008481.4:g.151130dup , LRG_130:g.151130dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2721dup	ENSP00000484935.2:n.2721dup
ENST00000504915.3:c.3110dup	ENSP00000473355.2:p.Glu1038ArgfsTer9
ENST00000505350.2:c.*3062dup	ENSP00000481752.1:n.*3062dup
ENST00000507379.6:c.3002dup	ENSP00000423224.2:p.Glu1002ArgfsTer9
ENST00000509732.6:c.3056dup	ENSP00000426541.2:p.Glu1020ArgfsTer9
ENST00000512211.7:c.3056dup	ENSP00000423828.3:p.Glu1020ArgfsTer9
ENST00000257430.9:c.3056dup MANE Select	ENSP00000257430.4:p.Glu1020ArgfsTer9
ENST00000257430.8:c.3056dup	ENSP00000257430.4:p.Glu1020ArgfsTer9
ENST00000502371.2:c.1409dup
ENST00000507379.5:c.3002dup	ENSP00000423224.1:p.Glu1002ArgfsTer9
ENST00000508376.6:c.3056dup	ENSP00000427089.2:p.Glu1020ArgfsTer9
ENST00000508624.5:c.*2378dup	ENSP00000424265.1:n.*2378dup
ENST00000512211.6:c.3056dup	ENSP00000423828.2:p.Glu1020ArgfsTer9
ENST00000520401.1:c.230+9678dup
NM_000038.5:c.3056dup	NP_000029.2:p.Glu1020ArgfsTer9
NM_001127510.2:c.3056dup	NP_001120982.1:p.Glu1020ArgfsTer9
NM_001127511.2:c.3002dup	NP_001120983.2:p.Glu1002ArgfsTer9
NM_001354895.1:c.3056dup	NP_001341824.1:p.Glu1020ArgfsTer9
NM_001354896.1:c.3110dup	NP_001341825.1:p.Glu1038ArgfsTer9
NM_001354897.1:c.3086dup	NP_001341826.1:p.Glu1030ArgfsTer9
NM_001354898.1:c.2981dup	NP_001341827.1:p.Glu995ArgfsTer9
NM_001354899.1:c.2972dup	NP_001341828.1:p.Glu992ArgfsTer9
NM_001354900.1:c.2933dup	NP_001341829.1:p.Glu979ArgfsTer9
NM_001354901.1:c.2879dup	NP_001341830.1:p.Glu961ArgfsTer9
NM_001354902.1:c.2783dup	NP_001341831.1:p.Glu929ArgfsTer9
NM_001354903.1:c.2753dup	NP_001341832.1:p.Glu919ArgfsTer9
NM_001354904.1:c.2678dup	NP_001341833.1:p.Glu894ArgfsTer9
NM_001354905.1:c.2576dup	NP_001341834.1:p.Glu860ArgfsTer9
NM_001354906.1:c.2207dup	NP_001341835.1:p.Glu737ArgfsTer9
NM_000038.6:c.3056dup MANE Select	NP_000029.2:p.Glu1020ArgfsTer9
NM_001127510.3:c.3056dup	NP_001120982.1:p.Glu1020ArgfsTer9
NM_001127511.3:c.3002dup	NP_001120983.2:p.Glu1002ArgfsTer9
NM_001354895.2:c.3056dup	NP_001341824.1:p.Glu1020ArgfsTer9
NM_001354896.2:c.3110dup	NP_001341825.1:p.Glu1038ArgfsTer9
NM_001354897.2:c.3086dup	NP_001341826.1:p.Glu1030ArgfsTer9
NM_001354898.2:c.2981dup	NP_001341827.1:p.Glu995ArgfsTer9
NM_001354899.2:c.2972dup	NP_001341828.1:p.Glu992ArgfsTer9
NM_001354900.2:c.2933dup	NP_001341829.1:p.Glu979ArgfsTer9
NM_001354901.2:c.2879dup	NP_001341830.1:p.Glu961ArgfsTer9
NM_001354902.2:c.2783dup	NP_001341831.1:p.Glu929ArgfsTer9
NM_001354903.2:c.2753dup	NP_001341832.1:p.Glu919ArgfsTer9
NM_001354904.2:c.2678dup	NP_001341833.1:p.Glu894ArgfsTer9
NM_001354905.2:c.2576dup	NP_001341834.1:p.Glu860ArgfsTer9
NM_001354906.2:c.2207dup	NP_001341835.1:p.Glu737ArgfsTer9