Canonical Allele Identifier: CA658760913

Gene: APC

Linked Data

• PubMed: PMID:11247896

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838988del , CM000667.2:g.112838988del	GRCh38
NC_000005.9:g.112174685del , CM000667.1:g.112174685del	GRCh37
NC_000005.8:g.112202584del	NCBI36
NG_008481.4:g.151468del , LRG_130:g.151468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3059del	ENSP00000484935.2:n.3059del
ENST00000504915.3:c.3448del	ENSP00000473355.2:p.Glu1150LysfsTer?
ENST00000505350.2:c.*3400del	ENSP00000481752.1:n.*3400del
ENST00000507379.6:c.3340del	ENSP00000423224.2:p.Glu1114LysfsTer?
ENST00000509732.6:c.3394del	ENSP00000426541.2:p.Glu1132LysfsTer?
ENST00000512211.7:c.3394del	ENSP00000423828.3:p.Glu1132LysfsTer?
ENST00000257430.9:c.3394del MANE Select	ENSP00000257430.4:p.Glu1132LysfsTer?
ENST00000257430.8:c.3394del	ENSP00000257430.4:p.Glu1132LysfsTer?
ENST00000502371.2:c.1747del
ENST00000507379.5:c.3340del	ENSP00000423224.1:p.Glu1114LysfsTer?
ENST00000508376.6:c.3394del	ENSP00000427089.2:p.Glu1132LysfsTer?
ENST00000508624.5:c.*2716del	ENSP00000424265.1:n.*2716del
ENST00000512211.6:c.3394del	ENSP00000423828.2:p.Glu1132LysfsTer?
ENST00000520401.1:c.230+10016del
NM_000038.5:c.3394del	NP_000029.2:p.Glu1132LysfsTer?
NM_001127510.2:c.3394del	NP_001120982.1:p.Glu1132LysfsTer?
NM_001127511.2:c.3340del	NP_001120983.2:p.Glu1114LysfsTer?
NM_001354895.1:c.3394del	NP_001341824.1:p.Glu1132LysfsTer?
NM_001354896.1:c.3448del	NP_001341825.1:p.Glu1150LysfsTer?
NM_001354897.1:c.3424del	NP_001341826.1:p.Glu1142LysfsTer?
NM_001354898.1:c.3319del	NP_001341827.1:p.Glu1107LysfsTer?
NM_001354899.1:c.3310del	NP_001341828.1:p.Glu1104LysfsTer?
NM_001354900.1:c.3271del	NP_001341829.1:p.Glu1091LysfsTer?
NM_001354901.1:c.3217del	NP_001341830.1:p.Glu1073LysfsTer?
NM_001354902.1:c.3121del	NP_001341831.1:p.Glu1041LysfsTer?
NM_001354903.1:c.3091del	NP_001341832.1:p.Glu1031LysfsTer?
NM_001354904.1:c.3016del	NP_001341833.1:p.Glu1006LysfsTer?
NM_001354905.1:c.2914del	NP_001341834.1:p.Glu972LysfsTer?
NM_001354906.1:c.2545del	NP_001341835.1:p.Glu849LysfsTer?
NM_000038.6:c.3394del MANE Select	NP_000029.2:p.Glu1132LysfsTer?
NM_001127510.3:c.3394del	NP_001120982.1:p.Glu1132LysfsTer?
NM_001127511.3:c.3340del	NP_001120983.2:p.Glu1114LysfsTer?
NM_001354895.2:c.3394del	NP_001341824.1:p.Glu1132LysfsTer?
NM_001354896.2:c.3448del	NP_001341825.1:p.Glu1150LysfsTer?
NM_001354897.2:c.3424del	NP_001341826.1:p.Glu1142LysfsTer?
NM_001354898.2:c.3319del	NP_001341827.1:p.Glu1107LysfsTer?
NM_001354899.2:c.3310del	NP_001341828.1:p.Glu1104LysfsTer?
NM_001354900.2:c.3271del	NP_001341829.1:p.Glu1091LysfsTer?
NM_001354901.2:c.3217del	NP_001341830.1:p.Glu1073LysfsTer?
NM_001354902.2:c.3121del	NP_001341831.1:p.Glu1041LysfsTer?
NM_001354903.2:c.3091del	NP_001341832.1:p.Glu1031LysfsTer?
NM_001354904.2:c.3016del	NP_001341833.1:p.Glu1006LysfsTer?
NM_001354905.2:c.2914del	NP_001341834.1:p.Glu972LysfsTer?
NM_001354906.2:c.2545del	NP_001341835.1:p.Glu849LysfsTer?