Canonical Allele Identifier: CA2695202731

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821953_112821954insG , CM000667.2:g.112821953_112821954insG	GRCh38
NC_000005.9:g.112157650_112157651insG , CM000667.1:g.112157650_112157651insG	GRCh37
NC_000005.8:g.112185549_112185550insG	NCBI36
NG_008481.4:g.134433_134434insG , LRG_130:g.134433_134434insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1370_1371insG	ENSP00000484935.2:p.Phe458IlefsTer2
ENST00000504915.3:c.1370_1371insG	ENSP00000473355.2:p.Phe458IlefsTer2
ENST00000505084.2:n.1426_1427insG
ENST00000505350.2:c.*1376_*1377insG	ENSP00000481752.1:n.*1376_*1377insG
ENST00000507379.6:c.1316_1317insG	ENSP00000423224.2:p.Phe440IlefsTer2
ENST00000509732.6:c.1370_1371insG	ENSP00000426541.2:p.Phe458IlefsTer2
ENST00000512211.7:c.1370_1371insG	ENSP00000423828.3:p.Phe458IlefsTer2
ENST00000257430.9:c.1370_1371insG MANE Select	ENSP00000257430.4:p.Phe458IlefsTer2
ENST00000257430.8:c.1370_1371insG	ENSP00000257430.4:p.Phe458IlefsTer2
ENST00000502371.2:c.58_59insG
ENST00000504915.2:c.5_6insG	ENSP00000473355.1:p.Phe3IlefsTer2
ENST00000507379.5:c.1316_1317insG	ENSP00000423224.1:p.Phe440IlefsTer2
ENST00000508376.6:c.1370_1371insG	ENSP00000427089.2:p.Phe458IlefsTer2
ENST00000508624.5:c.*692_*693insG	ENSP00000424265.1:n.*692_*693insG
ENST00000512211.6:c.1370_1371insG	ENSP00000423828.2:p.Phe458IlefsTer2
NM_000038.5:c.1370_1371insG	NP_000029.2:p.Phe458IlefsTer2
NM_001127510.2:c.1370_1371insG	NP_001120982.1:p.Phe458IlefsTer2
NM_001127511.2:c.1316_1317insG	NP_001120983.2:p.Phe440IlefsTer2
NM_001354895.1:c.1370_1371insG	NP_001341824.1:p.Phe458IlefsTer2
NM_001354896.1:c.1370_1371insG	NP_001341825.1:p.Phe458IlefsTer2
NM_001354897.1:c.1400_1401insG	NP_001341826.1:p.Phe468IlefsTer2
NM_001354898.1:c.1295_1296insG	NP_001341827.1:p.Phe433IlefsTer2
NM_001354899.1:c.1286_1287insG	NP_001341828.1:p.Phe430IlefsTer2
NM_001354900.1:c.1193_1194insG	NP_001341829.1:p.Phe399IlefsTer2
NM_001354901.1:c.1193_1194insG	NP_001341830.1:p.Phe399IlefsTer2
NM_001354902.1:c.1097_1098insG	NP_001341831.1:p.Phe367IlefsTer2
NM_001354903.1:c.1067_1068insG	NP_001341832.1:p.Phe357IlefsTer2
NM_001354904.1:c.992_993insG	NP_001341833.1:p.Phe332IlefsTer2
NM_001354905.1:c.890_891insG	NP_001341834.1:p.Phe298IlefsTer2
NM_001354906.1:c.521_522insG	NP_001341835.1:p.Phe175IlefsTer2
NM_000038.6:c.1370_1371insG MANE Select	NP_000029.2:p.Phe458IlefsTer2
NM_001127510.3:c.1370_1371insG	NP_001120982.1:p.Phe458IlefsTer2
NM_001127511.3:c.1316_1317insG	NP_001120983.2:p.Phe440IlefsTer2
NM_001354895.2:c.1370_1371insG	NP_001341824.1:p.Phe458IlefsTer2
NM_001354896.2:c.1370_1371insG	NP_001341825.1:p.Phe458IlefsTer2
NM_001354897.2:c.1400_1401insG	NP_001341826.1:p.Phe468IlefsTer2
NM_001354898.2:c.1295_1296insG	NP_001341827.1:p.Phe433IlefsTer2
NM_001354899.2:c.1286_1287insG	NP_001341828.1:p.Phe430IlefsTer2
NM_001354900.2:c.1193_1194insG	NP_001341829.1:p.Phe399IlefsTer2
NM_001354901.2:c.1193_1194insG	NP_001341830.1:p.Phe399IlefsTer2
NM_001354902.2:c.1097_1098insG	NP_001341831.1:p.Phe367IlefsTer2
NM_001354903.2:c.1067_1068insG	NP_001341832.1:p.Phe357IlefsTer2
NM_001354904.2:c.992_993insG	NP_001341833.1:p.Phe332IlefsTer2
NM_001354905.2:c.890_891insG	NP_001341834.1:p.Phe298IlefsTer2
NM_001354906.2:c.521_522insG	NP_001341835.1:p.Phe175IlefsTer2