Canonical Allele Identifier: CA2695204969

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839392_112839411dup , CM000667.2:g.112839392_112839411dup	GRCh38
NC_000005.9:g.112175089_112175108dup , CM000667.1:g.112175089_112175108dup	GRCh37
NC_000005.8:g.112202988_112203007dup	NCBI36
NG_008481.4:g.151872_151891dup , LRG_130:g.151872_151891dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3463_3482dup	ENSP00000484935.2:n.3463_3482dup
ENST00000504915.3:c.3852_3871dup	ENSP00000473355.2:p.Arg1291IlefsTer22
ENST00000505350.2:c.*3804_*3823dup	ENSP00000481752.1:n.*3804_*3823dup
ENST00000507379.6:c.3744_3763dup	ENSP00000423224.2:p.Arg1255IlefsTer22
ENST00000509732.6:c.3798_3817dup	ENSP00000426541.2:p.Arg1273IlefsTer22
ENST00000512211.7:c.3798_3817dup	ENSP00000423828.3:p.Arg1273IlefsTer22
ENST00000257430.9:c.3798_3817dup MANE Select	ENSP00000257430.4:p.Arg1273IlefsTer22
ENST00000257430.8:c.3798_3817dup	ENSP00000257430.4:p.Arg1273IlefsTer22
ENST00000502371.2:c.2151_2170dup
ENST00000508376.6:c.3798_3817dup	ENSP00000427089.2:p.Arg1273IlefsTer22
ENST00000508624.5:c.*3120_*3139dup	ENSP00000424265.1:n.*3120_*3139dup
ENST00000512211.6:c.3798_3817dup	ENSP00000423828.2:p.Arg1273IlefsTer22
ENST00000520401.1:c.230+10420_230+10439dup
NM_000038.5:c.3798_3817dup	NP_000029.2:p.Arg1273IlefsTer22
NM_001127510.2:c.3798_3817dup	NP_001120982.1:p.Arg1273IlefsTer22
NM_001127511.2:c.3744_3763dup	NP_001120983.2:p.Arg1255IlefsTer22
NM_001354895.1:c.3798_3817dup	NP_001341824.1:p.Arg1273IlefsTer22
NM_001354896.1:c.3852_3871dup	NP_001341825.1:p.Arg1291IlefsTer22
NM_001354897.1:c.3828_3847dup	NP_001341826.1:p.Arg1283IlefsTer22
NM_001354898.1:c.3723_3742dup	NP_001341827.1:p.Arg1248IlefsTer22
NM_001354899.1:c.3714_3733dup	NP_001341828.1:p.Arg1245IlefsTer22
NM_001354900.1:c.3675_3694dup	NP_001341829.1:p.Arg1232IlefsTer22
NM_001354901.1:c.3621_3640dup	NP_001341830.1:p.Arg1214IlefsTer22
NM_001354902.1:c.3525_3544dup	NP_001341831.1:p.Arg1182IlefsTer22
NM_001354903.1:c.3495_3514dup	NP_001341832.1:p.Arg1172IlefsTer22
NM_001354904.1:c.3420_3439dup	NP_001341833.1:p.Arg1147IlefsTer22
NM_001354905.1:c.3318_3337dup	NP_001341834.1:p.Arg1113IlefsTer22
NM_001354906.1:c.2949_2968dup	NP_001341835.1:p.Arg990IlefsTer22
NM_000038.6:c.3798_3817dup MANE Select	NP_000029.2:p.Arg1273IlefsTer22
NM_001127510.3:c.3798_3817dup	NP_001120982.1:p.Arg1273IlefsTer22
NM_001127511.3:c.3744_3763dup	NP_001120983.2:p.Arg1255IlefsTer22
NM_001354895.2:c.3798_3817dup	NP_001341824.1:p.Arg1273IlefsTer22
NM_001354896.2:c.3852_3871dup	NP_001341825.1:p.Arg1291IlefsTer22
NM_001354897.2:c.3828_3847dup	NP_001341826.1:p.Arg1283IlefsTer22
NM_001354898.2:c.3723_3742dup	NP_001341827.1:p.Arg1248IlefsTer22
NM_001354899.2:c.3714_3733dup	NP_001341828.1:p.Arg1245IlefsTer22
NM_001354900.2:c.3675_3694dup	NP_001341829.1:p.Arg1232IlefsTer22
NM_001354901.2:c.3621_3640dup	NP_001341830.1:p.Arg1214IlefsTer22
NM_001354902.2:c.3525_3544dup	NP_001341831.1:p.Arg1182IlefsTer22
NM_001354903.2:c.3495_3514dup	NP_001341832.1:p.Arg1172IlefsTer22
NM_001354904.2:c.3420_3439dup	NP_001341833.1:p.Arg1147IlefsTer22
NM_001354905.2:c.3318_3337dup	NP_001341834.1:p.Arg1113IlefsTer22
NM_001354906.2:c.2949_2968dup	NP_001341835.1:p.Arg990IlefsTer22