Canonical Allele Identifier: CA2514316463

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843471del , CM000667.2:g.112843471del	GRCh38
NC_000005.9:g.112179168del , CM000667.1:g.112179168del	GRCh37
NC_000005.8:g.112207067del	NCBI36
NG_008481.4:g.155951del , LRG_130:g.155951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7931del	ENSP00000473355.2:p.Thr2644IlefsTer18
ENST00000505350.2:c.*7883del	ENSP00000481752.1:n.*7883del
ENST00000507379.6:c.7823del	ENSP00000423224.2:p.Thr2608IlefsTer18
ENST00000509732.6:c.7877del	ENSP00000426541.2:p.Thr2626IlefsTer18
ENST00000512211.7:c.7877del	ENSP00000423828.3:p.Thr2626IlefsTer18
ENST00000257430.9:c.7877del MANE Select	ENSP00000257430.4:p.Thr2626IlefsTer18
ENST00000257430.8:c.7877del	ENSP00000257430.4:p.Thr2626IlefsTer18
ENST00000508376.6:c.7877del	ENSP00000427089.2:p.Thr2626IlefsTer18
ENST00000520401.1:c.231-13178del
NM_000038.5:c.7877del	NP_000029.2:p.Thr2626IlefsTer18
NM_001127510.2:c.7877del	NP_001120982.1:p.Thr2626IlefsTer18
NM_001127511.2:c.7823del	NP_001120983.2:p.Thr2608IlefsTer18
NM_001354895.1:c.7877del	NP_001341824.1:p.Thr2626IlefsTer18
NM_001354896.1:c.7931del	NP_001341825.1:p.Thr2644IlefsTer18
NM_001354897.1:c.7907del	NP_001341826.1:p.Thr2636IlefsTer18
NM_001354898.1:c.7802del	NP_001341827.1:p.Thr2601IlefsTer18
NM_001354899.1:c.7793del	NP_001341828.1:p.Thr2598IlefsTer18
NM_001354900.1:c.7754del	NP_001341829.1:p.Thr2585IlefsTer18
NM_001354901.1:c.7700del	NP_001341830.1:p.Thr2567IlefsTer18
NM_001354902.1:c.7604del	NP_001341831.1:p.Thr2535IlefsTer18
NM_001354903.1:c.7574del	NP_001341832.1:p.Thr2525IlefsTer18
NM_001354904.1:c.7499del	NP_001341833.1:p.Thr2500IlefsTer18
NM_001354905.1:c.7397del	NP_001341834.1:p.Thr2466IlefsTer18
NM_001354906.1:c.7028del	NP_001341835.1:p.Thr2343IlefsTer18
NM_000038.6:c.7877del MANE Select	NP_000029.2:p.Thr2626IlefsTer18
NM_001127510.3:c.7877del	NP_001120982.1:p.Thr2626IlefsTer18
NM_001127511.3:c.7823del	NP_001120983.2:p.Thr2608IlefsTer18
NM_001354895.2:c.7877del	NP_001341824.1:p.Thr2626IlefsTer18
NM_001354896.2:c.7931del	NP_001341825.1:p.Thr2644IlefsTer18
NM_001354897.2:c.7907del	NP_001341826.1:p.Thr2636IlefsTer18
NM_001354898.2:c.7802del	NP_001341827.1:p.Thr2601IlefsTer18
NM_001354899.2:c.7793del	NP_001341828.1:p.Thr2598IlefsTer18
NM_001354900.2:c.7754del	NP_001341829.1:p.Thr2585IlefsTer18
NM_001354901.2:c.7700del	NP_001341830.1:p.Thr2567IlefsTer18
NM_001354902.2:c.7604del	NP_001341831.1:p.Thr2535IlefsTer18
NM_001354903.2:c.7574del	NP_001341832.1:p.Thr2525IlefsTer18
NM_001354904.2:c.7499del	NP_001341833.1:p.Thr2500IlefsTer18
NM_001354905.2:c.7397del	NP_001341834.1:p.Thr2466IlefsTer18
NM_001354906.2:c.7028del	NP_001341835.1:p.Thr2343IlefsTer18