Canonical Allele Identifier: CA658760547

Gene: APC

Linked Data

• PubMed: PMID:8187091 ; PMID:10768871

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819271_112819281del , CM000667.2:g.112819271_112819281del	GRCh38
NC_000005.9:g.112154968_112154978del , CM000667.1:g.112154968_112154978del	GRCh37
NC_000005.8:g.112182867_112182877del	NCBI36
NG_008481.4:g.131751_131761del , LRG_130:g.131751_131761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1239_1249del	ENSP00000484935.2:p.Ile413MetfsTer2
ENST00000504915.3:c.1239_1249del	ENSP00000473355.2:p.Ile413MetfsTer2
ENST00000505084.2:n.1295_1305del
ENST00000505350.2:c.*1245_*1255del	ENSP00000481752.1:n.*1245_*1255del
ENST00000507379.6:c.1185_1195del	ENSP00000423224.2:p.Ile395MetfsTer2
ENST00000509732.6:c.1239_1249del	ENSP00000426541.2:p.Ile413MetfsTer2
ENST00000512211.7:c.1239_1249del	ENSP00000423828.3:p.Ile413MetfsTer2
ENST00000257430.9:c.1239_1249del MANE Select	ENSP00000257430.4:p.Ile413MetfsTer2
ENST00000257430.8:c.1239_1249del	ENSP00000257430.4:p.Ile413MetfsTer2
ENST00000507379.5:c.1185_1195del	ENSP00000423224.1:p.Ile395MetfsTer2
ENST00000508376.6:c.1239_1249del	ENSP00000427089.2:p.Ile413MetfsTer2
ENST00000508624.5:c.*561_*571del	ENSP00000424265.1:n.*561_*571del
ENST00000512211.6:c.1239_1249del	ENSP00000423828.2:p.Ile413MetfsTer2
NM_000038.5:c.1239_1249del	NP_000029.2:p.Ile413MetfsTer2
NM_001127510.2:c.1239_1249del	NP_001120982.1:p.Ile413MetfsTer2
NM_001127511.2:c.1185_1195del	NP_001120983.2:p.Ile395MetfsTer2
NM_001354895.1:c.1239_1249del	NP_001341824.1:p.Ile413MetfsTer2
NM_001354896.1:c.1239_1249del	NP_001341825.1:p.Ile413MetfsTer2
NM_001354897.1:c.1269_1279del	NP_001341826.1:p.Ile423MetfsTer2
NM_001354898.1:c.1164_1174del	NP_001341827.1:p.Ile388MetfsTer2
NM_001354899.1:c.1155_1165del	NP_001341828.1:p.Ile385MetfsTer2
NM_001354900.1:c.1062_1072del	NP_001341829.1:p.Ile354MetfsTer2
NM_001354901.1:c.1062_1072del	NP_001341830.1:p.Ile354MetfsTer2
NM_001354902.1:c.966_976del	NP_001341831.1:p.Ile322MetfsTer2
NM_001354903.1:c.936_946del	NP_001341832.1:p.Ile312MetfsTer2
NM_001354904.1:c.861_871del	NP_001341833.1:p.Ile287MetfsTer2
NM_001354905.1:c.759_769del	NP_001341834.1:p.Ile253MetfsTer2
NM_001354906.1:c.390_400del	NP_001341835.1:p.Ile130MetfsTer2
NM_000038.6:c.1239_1249del MANE Select	NP_000029.2:p.Ile413MetfsTer2
NM_001127510.3:c.1239_1249del	NP_001120982.1:p.Ile413MetfsTer2
NM_001127511.3:c.1185_1195del	NP_001120983.2:p.Ile395MetfsTer2
NM_001354895.2:c.1239_1249del	NP_001341824.1:p.Ile413MetfsTer2
NM_001354896.2:c.1239_1249del	NP_001341825.1:p.Ile413MetfsTer2
NM_001354897.2:c.1269_1279del	NP_001341826.1:p.Ile423MetfsTer2
NM_001354898.2:c.1164_1174del	NP_001341827.1:p.Ile388MetfsTer2
NM_001354899.2:c.1155_1165del	NP_001341828.1:p.Ile385MetfsTer2
NM_001354900.2:c.1062_1072del	NP_001341829.1:p.Ile354MetfsTer2
NM_001354901.2:c.1062_1072del	NP_001341830.1:p.Ile354MetfsTer2
NM_001354902.2:c.966_976del	NP_001341831.1:p.Ile322MetfsTer2
NM_001354903.2:c.936_946del	NP_001341832.1:p.Ile312MetfsTer2
NM_001354904.2:c.861_871del	NP_001341833.1:p.Ile287MetfsTer2
NM_001354905.2:c.759_769del	NP_001341834.1:p.Ile253MetfsTer2
NM_001354906.2:c.390_400del	NP_001341835.1:p.Ile130MetfsTer2