Canonical Allele Identifier: CA2695204980

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843620_112843634del , CM000667.2:g.112843620_112843634del	GRCh38
NC_000005.9:g.112179317_112179331del , CM000667.1:g.112179317_112179331del	GRCh37
NC_000005.8:g.112207216_112207230del	NCBI36
NG_008481.4:g.156100_156114del , LRG_130:g.156100_156114del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.8080_8094del	ENSP00000473355.2:p.Thr2694_Pro2698del
ENST00000505350.2:c.*8032_*8046del	ENSP00000481752.1:n.*8032_*8046del
ENST00000507379.6:c.7972_7986del	ENSP00000423224.2:p.Thr2658_Pro2662del
ENST00000509732.6:c.8026_8040del	ENSP00000426541.2:p.Thr2676_Pro2680del
ENST00000512211.7:c.8026_8040del	ENSP00000423828.3:p.Thr2676_Pro2680del
ENST00000257430.9:c.8026_8040del MANE Select	ENSP00000257430.4:p.Thr2676_Pro2680del
ENST00000257430.8:c.8026_8040del	ENSP00000257430.4:p.Thr2676_Pro2680del
ENST00000508376.6:c.8026_8040del	ENSP00000427089.2:p.Thr2676_Pro2680del
ENST00000520401.1:c.231-13029_231-13015del
NM_000038.5:c.8026_8040del	NP_000029.2:p.Thr2676_Pro2680del
NM_001127510.2:c.8026_8040del	NP_001120982.1:p.Thr2676_Pro2680del
NM_001127511.2:c.7972_7986del	NP_001120983.2:p.Thr2658_Pro2662del
NM_001354895.1:c.8026_8040del	NP_001341824.1:p.Thr2676_Pro2680del
NM_001354896.1:c.8080_8094del	NP_001341825.1:p.Thr2694_Pro2698del
NM_001354897.1:c.8056_8070del	NP_001341826.1:p.Thr2686_Pro2690del
NM_001354898.1:c.7951_7965del	NP_001341827.1:p.Thr2651_Pro2655del
NM_001354899.1:c.7942_7956del	NP_001341828.1:p.Thr2648_Pro2652del
NM_001354900.1:c.7903_7917del	NP_001341829.1:p.Thr2635_Pro2639del
NM_001354901.1:c.7849_7863del	NP_001341830.1:p.Thr2617_Pro2621del
NM_001354902.1:c.7753_7767del	NP_001341831.1:p.Thr2585_Pro2589del
NM_001354903.1:c.7723_7737del	NP_001341832.1:p.Thr2575_Pro2579del
NM_001354904.1:c.7648_7662del	NP_001341833.1:p.Thr2550_Pro2554del
NM_001354905.1:c.7546_7560del	NP_001341834.1:p.Thr2516_Pro2520del
NM_001354906.1:c.7177_7191del	NP_001341835.1:p.Thr2393_Pro2397del
NM_000038.6:c.8026_8040del MANE Select	NP_000029.2:p.Thr2676_Pro2680del
NM_001127510.3:c.8026_8040del	NP_001120982.1:p.Thr2676_Pro2680del
NM_001127511.3:c.7972_7986del	NP_001120983.2:p.Thr2658_Pro2662del
NM_001354895.2:c.8026_8040del	NP_001341824.1:p.Thr2676_Pro2680del
NM_001354896.2:c.8080_8094del	NP_001341825.1:p.Thr2694_Pro2698del
NM_001354897.2:c.8056_8070del	NP_001341826.1:p.Thr2686_Pro2690del
NM_001354898.2:c.7951_7965del	NP_001341827.1:p.Thr2651_Pro2655del
NM_001354899.2:c.7942_7956del	NP_001341828.1:p.Thr2648_Pro2652del
NM_001354900.2:c.7903_7917del	NP_001341829.1:p.Thr2635_Pro2639del
NM_001354901.2:c.7849_7863del	NP_001341830.1:p.Thr2617_Pro2621del
NM_001354902.2:c.7753_7767del	NP_001341831.1:p.Thr2585_Pro2589del
NM_001354903.2:c.7723_7737del	NP_001341832.1:p.Thr2575_Pro2579del
NM_001354904.2:c.7648_7662del	NP_001341833.1:p.Thr2550_Pro2554del
NM_001354905.2:c.7546_7560del	NP_001341834.1:p.Thr2516_Pro2520del
NM_001354906.2:c.7177_7191del	NP_001341835.1:p.Thr2393_Pro2397del