Canonical Allele Identifier: CA658760929

Gene: APC

Linked Data

• PubMed: PMID:17411426

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839107dup , CM000667.2:g.112839107dup	GRCh38
NC_000005.9:g.112174804dup , CM000667.1:g.112174804dup	GRCh37
NC_000005.8:g.112202703dup	NCBI36
NG_008481.4:g.151587dup , LRG_130:g.151587dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3178dup	ENSP00000484935.2:n.3178dup
ENST00000504915.3:c.3567dup	ENSP00000473355.2:p.His1190SerfsTer7
ENST00000505350.2:c.*3519dup	ENSP00000481752.1:n.*3519dup
ENST00000507379.6:c.3459dup	ENSP00000423224.2:p.His1154SerfsTer7
ENST00000509732.6:c.3513dup	ENSP00000426541.2:p.His1172SerfsTer7
ENST00000512211.7:c.3513dup	ENSP00000423828.3:p.His1172SerfsTer7
ENST00000257430.9:c.3513dup MANE Select	ENSP00000257430.4:p.His1172SerfsTer7
ENST00000257430.8:c.3513dup	ENSP00000257430.4:p.His1172SerfsTer7
ENST00000502371.2:c.1866dup
ENST00000508376.6:c.3513dup	ENSP00000427089.2:p.His1172SerfsTer7
ENST00000508624.5:c.*2835dup	ENSP00000424265.1:n.*2835dup
ENST00000512211.6:c.3513dup	ENSP00000423828.2:p.His1172SerfsTer7
ENST00000520401.1:c.230+10135dup
NM_000038.5:c.3513dup	NP_000029.2:p.His1172SerfsTer7
NM_001127510.2:c.3513dup	NP_001120982.1:p.His1172SerfsTer7
NM_001127511.2:c.3459dup	NP_001120983.2:p.His1154SerfsTer7
NM_001354895.1:c.3513dup	NP_001341824.1:p.His1172SerfsTer7
NM_001354896.1:c.3567dup	NP_001341825.1:p.His1190SerfsTer7
NM_001354897.1:c.3543dup	NP_001341826.1:p.His1182SerfsTer7
NM_001354898.1:c.3438dup	NP_001341827.1:p.His1147SerfsTer7
NM_001354899.1:c.3429dup	NP_001341828.1:p.His1144SerfsTer7
NM_001354900.1:c.3390dup	NP_001341829.1:p.His1131SerfsTer7
NM_001354901.1:c.3336dup	NP_001341830.1:p.His1113SerfsTer7
NM_001354902.1:c.3240dup	NP_001341831.1:p.His1081SerfsTer7
NM_001354903.1:c.3210dup	NP_001341832.1:p.His1071SerfsTer7
NM_001354904.1:c.3135dup	NP_001341833.1:p.His1046SerfsTer7
NM_001354905.1:c.3033dup	NP_001341834.1:p.His1012SerfsTer7
NM_001354906.1:c.2664dup	NP_001341835.1:p.His889SerfsTer7
NM_000038.6:c.3513dup MANE Select	NP_000029.2:p.His1172SerfsTer7
NM_001127510.3:c.3513dup	NP_001120982.1:p.His1172SerfsTer7
NM_001127511.3:c.3459dup	NP_001120983.2:p.His1154SerfsTer7
NM_001354895.2:c.3513dup	NP_001341824.1:p.His1172SerfsTer7
NM_001354896.2:c.3567dup	NP_001341825.1:p.His1190SerfsTer7
NM_001354897.2:c.3543dup	NP_001341826.1:p.His1182SerfsTer7
NM_001354898.2:c.3438dup	NP_001341827.1:p.His1147SerfsTer7
NM_001354899.2:c.3429dup	NP_001341828.1:p.His1144SerfsTer7
NM_001354900.2:c.3390dup	NP_001341829.1:p.His1131SerfsTer7
NM_001354901.2:c.3336dup	NP_001341830.1:p.His1113SerfsTer7
NM_001354902.2:c.3240dup	NP_001341831.1:p.His1081SerfsTer7
NM_001354903.2:c.3210dup	NP_001341832.1:p.His1071SerfsTer7
NM_001354904.2:c.3135dup	NP_001341833.1:p.His1046SerfsTer7
NM_001354905.2:c.3033dup	NP_001341834.1:p.His1012SerfsTer7
NM_001354906.2:c.2664dup	NP_001341835.1:p.His889SerfsTer7