Canonical Allele Identifier: CA645562852

Gene: APC

Linked Data - Expert Curation

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838215_112838220del , CM000667.2:g.112838215_112838220del	GRCh38
NC_000005.9:g.112173912_112173917del , CM000667.1:g.112173912_112173917del	GRCh37
NC_000005.8:g.112201811_112201816del	NCBI36
NG_008481.4:g.150695_150700del , LRG_130:g.150695_150700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2286_2291del	ENSP00000484935.2:n.2286_2291del
ENST00000504915.3:c.2675_2680del	ENSP00000473355.2:p.Ser892Ter
ENST00000505350.2:c.*2627_*2632del	ENSP00000481752.1:n.*2627_*2632del
ENST00000507379.6:c.2567_2572del	ENSP00000423224.2:p.Ser856Ter
ENST00000509732.6:c.2621_2626del	ENSP00000426541.2:p.Ser874Ter
ENST00000512211.7:c.2621_2626del	ENSP00000423828.3:p.Ser874Ter
ENST00000257430.9:c.2621_2626del MANE Select	ENSP00000257430.4:p.Ser874Ter
ENST00000257430.8:c.2621_2626del	ENSP00000257430.4:p.Ser874Ter
ENST00000502371.2:c.974_979del
ENST00000507379.5:c.2567_2572del	ENSP00000423224.1:p.Ser856Ter
ENST00000508376.6:c.2621_2626del	ENSP00000427089.2:p.Ser874Ter
ENST00000508624.5:c.*1943_*1948del	ENSP00000424265.1:n.*1943_*1948del
ENST00000512211.6:c.2621_2626del	ENSP00000423828.2:p.Ser874Ter
ENST00000520401.1:c.230+9243_230+9248del
NM_000038.5:c.2621_2626del	NP_000029.2:p.Ser874Ter
NM_001127510.2:c.2621_2626del	NP_001120982.1:p.Ser874Ter
NM_001127511.2:c.2567_2572del	NP_001120983.2:p.Ser856Ter
NM_001354895.1:c.2621_2626del	NP_001341824.1:p.Ser874Ter
NM_001354896.1:c.2675_2680del	NP_001341825.1:p.Ser892Ter
NM_001354897.1:c.2651_2656del	NP_001341826.1:p.Ser884Ter
NM_001354898.1:c.2546_2551del	NP_001341827.1:p.Ser849Ter
NM_001354899.1:c.2537_2542del	NP_001341828.1:p.Ser846Ter
NM_001354900.1:c.2498_2503del	NP_001341829.1:p.Ser833Ter
NM_001354901.1:c.2444_2449del	NP_001341830.1:p.Ser815Ter
NM_001354902.1:c.2348_2353del	NP_001341831.1:p.Ser783Ter
NM_001354903.1:c.2318_2323del	NP_001341832.1:p.Ser773Ter
NM_001354904.1:c.2243_2248del	NP_001341833.1:p.Ser748Ter
NM_001354905.1:c.2141_2146del	NP_001341834.1:p.Ser714Ter
NM_001354906.1:c.1772_1777del	NP_001341835.1:p.Ser591Ter
NM_000038.6:c.2621_2626del MANE Select	NP_000029.2:p.Ser874Ter
NM_001127510.3:c.2621_2626del	NP_001120982.1:p.Ser874Ter
NM_001127511.3:c.2567_2572del	NP_001120983.2:p.Ser856Ter
NM_001354895.2:c.2621_2626del	NP_001341824.1:p.Ser874Ter
NM_001354896.2:c.2675_2680del	NP_001341825.1:p.Ser892Ter
NM_001354897.2:c.2651_2656del	NP_001341826.1:p.Ser884Ter
NM_001354898.2:c.2546_2551del	NP_001341827.1:p.Ser849Ter
NM_001354899.2:c.2537_2542del	NP_001341828.1:p.Ser846Ter
NM_001354900.2:c.2498_2503del	NP_001341829.1:p.Ser833Ter
NM_001354901.2:c.2444_2449del	NP_001341830.1:p.Ser815Ter
NM_001354902.2:c.2348_2353del	NP_001341831.1:p.Ser783Ter
NM_001354903.2:c.2318_2323del	NP_001341832.1:p.Ser773Ter
NM_001354904.2:c.2243_2248del	NP_001341833.1:p.Ser748Ter
NM_001354905.2:c.2141_2146del	NP_001341834.1:p.Ser714Ter
NM_001354906.2:c.1772_1777del	NP_001341835.1:p.Ser591Ter