Canonical Allele Identifier: CA645543550

Gene: APC

Linked Data

• COSMIC: COSM5452944

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838646del , CM000667.2:g.112838646del	GRCh38
NC_000005.9:g.112174343del , CM000667.1:g.112174343del	GRCh37
NC_000005.8:g.112202242del	NCBI36
NG_008481.4:g.151126del , LRG_130:g.151126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2717del	ENSP00000484935.2:n.2717del
ENST00000504915.3:c.3106del	ENSP00000473355.2:p.Asp1036MetfsTer4
ENST00000505350.2:c.*3058del	ENSP00000481752.1:n.*3058del
ENST00000507379.6:c.2998del	ENSP00000423224.2:p.Asp1000MetfsTer4
ENST00000509732.6:c.3052del	ENSP00000426541.2:p.Asp1018MetfsTer4
ENST00000512211.7:c.3052del	ENSP00000423828.3:p.Asp1018MetfsTer4
ENST00000257430.9:c.3052del MANE Select	ENSP00000257430.4:p.Asp1018MetfsTer4
ENST00000257430.8:c.3052del	ENSP00000257430.4:p.Asp1018MetfsTer4
ENST00000502371.2:c.1405del
ENST00000507379.5:c.2998del	ENSP00000423224.1:p.Asp1000MetfsTer4
ENST00000508376.6:c.3052del	ENSP00000427089.2:p.Asp1018MetfsTer4
ENST00000508624.5:c.*2374del	ENSP00000424265.1:n.*2374del
ENST00000512211.6:c.3052del	ENSP00000423828.2:p.Asp1018MetfsTer4
ENST00000520401.1:c.230+9674del
NM_000038.5:c.3052del	NP_000029.2:p.Asp1018MetfsTer4
NM_001127510.2:c.3052del	NP_001120982.1:p.Asp1018MetfsTer4
NM_001127511.2:c.2998del	NP_001120983.2:p.Asp1000MetfsTer4
NM_001354895.1:c.3052del	NP_001341824.1:p.Asp1018MetfsTer4
NM_001354896.1:c.3106del	NP_001341825.1:p.Asp1036MetfsTer4
NM_001354897.1:c.3082del	NP_001341826.1:p.Asp1028MetfsTer4
NM_001354898.1:c.2977del	NP_001341827.1:p.Asp993MetfsTer4
NM_001354899.1:c.2968del	NP_001341828.1:p.Asp990MetfsTer4
NM_001354900.1:c.2929del	NP_001341829.1:p.Asp977MetfsTer4
NM_001354901.1:c.2875del	NP_001341830.1:p.Asp959MetfsTer4
NM_001354902.1:c.2779del	NP_001341831.1:p.Asp927MetfsTer4
NM_001354903.1:c.2749del	NP_001341832.1:p.Asp917MetfsTer4
NM_001354904.1:c.2674del	NP_001341833.1:p.Asp892MetfsTer4
NM_001354905.1:c.2572del	NP_001341834.1:p.Asp858MetfsTer4
NM_001354906.1:c.2203del	NP_001341835.1:p.Asp735MetfsTer4
NM_000038.6:c.3052del MANE Select	NP_000029.2:p.Asp1018MetfsTer4
NM_001127510.3:c.3052del	NP_001120982.1:p.Asp1018MetfsTer4
NM_001127511.3:c.2998del	NP_001120983.2:p.Asp1000MetfsTer4
NM_001354895.2:c.3052del	NP_001341824.1:p.Asp1018MetfsTer4
NM_001354896.2:c.3106del	NP_001341825.1:p.Asp1036MetfsTer4
NM_001354897.2:c.3082del	NP_001341826.1:p.Asp1028MetfsTer4
NM_001354898.2:c.2977del	NP_001341827.1:p.Asp993MetfsTer4
NM_001354899.2:c.2968del	NP_001341828.1:p.Asp990MetfsTer4
NM_001354900.2:c.2929del	NP_001341829.1:p.Asp977MetfsTer4
NM_001354901.2:c.2875del	NP_001341830.1:p.Asp959MetfsTer4
NM_001354902.2:c.2779del	NP_001341831.1:p.Asp927MetfsTer4
NM_001354903.2:c.2749del	NP_001341832.1:p.Asp917MetfsTer4
NM_001354904.2:c.2674del	NP_001341833.1:p.Asp892MetfsTer4
NM_001354905.2:c.2572del	NP_001341834.1:p.Asp858MetfsTer4
NM_001354906.2:c.2203del	NP_001341835.1:p.Asp735MetfsTer4