Canonical Allele Identifier: CA658760774

Gene: APC

Linked Data

• PubMed: PMID:20223039

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840283_112840298del , CM000667.2:g.112840283_112840298del	GRCh38
NC_000005.9:g.112175980_112175995del , CM000667.1:g.112175980_112175995del	GRCh37
NC_000005.8:g.112203879_112203894del	NCBI36
NG_008481.4:g.152763_152778del , LRG_130:g.152763_152778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4743_4758del	ENSP00000473355.2:p.Leu1582MetfsTer7
ENST00000505350.2:c.*4695_*4710del	ENSP00000481752.1:n.*4695_*4710del
ENST00000507379.6:c.4635_4650del	ENSP00000423224.2:p.Leu1546MetfsTer7
ENST00000509732.6:c.4689_4704del	ENSP00000426541.2:p.Leu1564MetfsTer7
ENST00000512211.7:c.4689_4704del	ENSP00000423828.3:p.Leu1564MetfsTer7
ENST00000257430.9:c.4689_4704del MANE Select	ENSP00000257430.4:p.Leu1564MetfsTer7
ENST00000257430.8:c.4689_4704del	ENSP00000257430.4:p.Leu1564MetfsTer7
ENST00000508376.6:c.4689_4704del	ENSP00000427089.2:p.Leu1564MetfsTer7
ENST00000508624.5:c.*4011_*4026del	ENSP00000424265.1:n.*4011_*4026del
ENST00000520401.1:c.230+11311_230+11326del
NM_000038.5:c.4689_4704del	NP_000029.2:p.Leu1564MetfsTer7
NM_001127510.2:c.4689_4704del	NP_001120982.1:p.Leu1564MetfsTer7
NM_001127511.2:c.4635_4650del	NP_001120983.2:p.Leu1546MetfsTer7
NM_001354895.1:c.4689_4704del	NP_001341824.1:p.Leu1564MetfsTer7
NM_001354896.1:c.4743_4758del	NP_001341825.1:p.Leu1582MetfsTer7
NM_001354897.1:c.4719_4734del	NP_001341826.1:p.Leu1574MetfsTer7
NM_001354898.1:c.4614_4629del	NP_001341827.1:p.Leu1539MetfsTer7
NM_001354899.1:c.4605_4620del	NP_001341828.1:p.Leu1536MetfsTer7
NM_001354900.1:c.4566_4581del	NP_001341829.1:p.Leu1523MetfsTer7
NM_001354901.1:c.4512_4527del	NP_001341830.1:p.Leu1505MetfsTer7
NM_001354902.1:c.4416_4431del	NP_001341831.1:p.Leu1473MetfsTer7
NM_001354903.1:c.4386_4401del	NP_001341832.1:p.Leu1463MetfsTer7
NM_001354904.1:c.4311_4326del	NP_001341833.1:p.Leu1438MetfsTer7
NM_001354905.1:c.4209_4224del	NP_001341834.1:p.Leu1404MetfsTer7
NM_001354906.1:c.3840_3855del	NP_001341835.1:p.Leu1281MetfsTer7
NM_000038.6:c.4689_4704del MANE Select	NP_000029.2:p.Leu1564MetfsTer7
NM_001127510.3:c.4689_4704del	NP_001120982.1:p.Leu1564MetfsTer7
NM_001127511.3:c.4635_4650del	NP_001120983.2:p.Leu1546MetfsTer7
NM_001354895.2:c.4689_4704del	NP_001341824.1:p.Leu1564MetfsTer7
NM_001354896.2:c.4743_4758del	NP_001341825.1:p.Leu1582MetfsTer7
NM_001354897.2:c.4719_4734del	NP_001341826.1:p.Leu1574MetfsTer7
NM_001354898.2:c.4614_4629del	NP_001341827.1:p.Leu1539MetfsTer7
NM_001354899.2:c.4605_4620del	NP_001341828.1:p.Leu1536MetfsTer7
NM_001354900.2:c.4566_4581del	NP_001341829.1:p.Leu1523MetfsTer7
NM_001354901.2:c.4512_4527del	NP_001341830.1:p.Leu1505MetfsTer7
NM_001354902.2:c.4416_4431del	NP_001341831.1:p.Leu1473MetfsTer7
NM_001354903.2:c.4386_4401del	NP_001341832.1:p.Leu1463MetfsTer7
NM_001354904.2:c.4311_4326del	NP_001341833.1:p.Leu1438MetfsTer7
NM_001354905.2:c.4209_4224del	NP_001341834.1:p.Leu1404MetfsTer7
NM_001354906.2:c.3840_3855del	NP_001341835.1:p.Leu1281MetfsTer7