Canonical Allele Identifier: CA658760863

Gene: APC

Linked Data

• PubMed: PMID:7833936

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838621_112838622dup , CM000667.2:g.112838621_112838622dup	GRCh38
NC_000005.9:g.112174318_112174319dup , CM000667.1:g.112174318_112174319dup	GRCh37
NC_000005.8:g.112202217_112202218dup	NCBI36
NG_008481.4:g.151101_151102dup , LRG_130:g.151101_151102dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2692_2693dup	ENSP00000484935.2:n.2692_2693dup
ENST00000504915.3:c.3081_3082dup	ENSP00000473355.2:p.Ser1028IlefsTer13
ENST00000505350.2:c.*3033_*3034dup	ENSP00000481752.1:n.*3033_*3034dup
ENST00000507379.6:c.2973_2974dup	ENSP00000423224.2:p.Ser992IlefsTer13
ENST00000509732.6:c.3027_3028dup	ENSP00000426541.2:p.Ser1010IlefsTer13
ENST00000512211.7:c.3027_3028dup	ENSP00000423828.3:p.Ser1010IlefsTer13
ENST00000257430.9:c.3027_3028dup MANE Select	ENSP00000257430.4:p.Ser1010IlefsTer13
ENST00000257430.8:c.3027_3028dup	ENSP00000257430.4:p.Ser1010IlefsTer13
ENST00000502371.2:c.1380_1381dup
ENST00000507379.5:c.2973_2974dup	ENSP00000423224.1:p.Ser992IlefsTer13
ENST00000508376.6:c.3027_3028dup	ENSP00000427089.2:p.Ser1010IlefsTer13
ENST00000508624.5:c.*2349_*2350dup	ENSP00000424265.1:n.*2349_*2350dup
ENST00000512211.6:c.3027_3028dup	ENSP00000423828.2:p.Ser1010IlefsTer13
ENST00000520401.1:c.230+9649_230+9650dup
NM_000038.5:c.3027_3028dup	NP_000029.2:p.Ser1010IlefsTer13
NM_001127510.2:c.3027_3028dup	NP_001120982.1:p.Ser1010IlefsTer13
NM_001127511.2:c.2973_2974dup	NP_001120983.2:p.Ser992IlefsTer13
NM_001354895.1:c.3027_3028dup	NP_001341824.1:p.Ser1010IlefsTer13
NM_001354896.1:c.3081_3082dup	NP_001341825.1:p.Ser1028IlefsTer13
NM_001354897.1:c.3057_3058dup	NP_001341826.1:p.Ser1020IlefsTer13
NM_001354898.1:c.2952_2953dup	NP_001341827.1:p.Ser985IlefsTer13
NM_001354899.1:c.2943_2944dup	NP_001341828.1:p.Ser982IlefsTer13
NM_001354900.1:c.2904_2905dup	NP_001341829.1:p.Ser969IlefsTer13
NM_001354901.1:c.2850_2851dup	NP_001341830.1:p.Ser951IlefsTer13
NM_001354902.1:c.2754_2755dup	NP_001341831.1:p.Ser919IlefsTer13
NM_001354903.1:c.2724_2725dup	NP_001341832.1:p.Ser909IlefsTer13
NM_001354904.1:c.2649_2650dup	NP_001341833.1:p.Ser884IlefsTer13
NM_001354905.1:c.2547_2548dup	NP_001341834.1:p.Ser850IlefsTer13
NM_001354906.1:c.2178_2179dup	NP_001341835.1:p.Ser727IlefsTer13
NM_000038.6:c.3027_3028dup MANE Select	NP_000029.2:p.Ser1010IlefsTer13
NM_001127510.3:c.3027_3028dup	NP_001120982.1:p.Ser1010IlefsTer13
NM_001127511.3:c.2973_2974dup	NP_001120983.2:p.Ser992IlefsTer13
NM_001354895.2:c.3027_3028dup	NP_001341824.1:p.Ser1010IlefsTer13
NM_001354896.2:c.3081_3082dup	NP_001341825.1:p.Ser1028IlefsTer13
NM_001354897.2:c.3057_3058dup	NP_001341826.1:p.Ser1020IlefsTer13
NM_001354898.2:c.2952_2953dup	NP_001341827.1:p.Ser985IlefsTer13
NM_001354899.2:c.2943_2944dup	NP_001341828.1:p.Ser982IlefsTer13
NM_001354900.2:c.2904_2905dup	NP_001341829.1:p.Ser969IlefsTer13
NM_001354901.2:c.2850_2851dup	NP_001341830.1:p.Ser951IlefsTer13
NM_001354902.2:c.2754_2755dup	NP_001341831.1:p.Ser919IlefsTer13
NM_001354903.2:c.2724_2725dup	NP_001341832.1:p.Ser909IlefsTer13
NM_001354904.2:c.2649_2650dup	NP_001341833.1:p.Ser884IlefsTer13
NM_001354905.2:c.2547_2548dup	NP_001341834.1:p.Ser850IlefsTer13
NM_001354906.2:c.2178_2179dup	NP_001341835.1:p.Ser727IlefsTer13