Canonical Allele Identifier: CA658760864

Gene: APC

Linked Data

• PubMed: PMID:11933206 ; PMID:15024739

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838644_112838647del , CM000667.2:g.112838644_112838647del	GRCh38
NC_000005.9:g.112174341_112174344del , CM000667.1:g.112174341_112174344del	GRCh37
NC_000005.8:g.112202240_112202243del	NCBI36
NG_008481.4:g.151124_151127del , LRG_130:g.151124_151127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2715_2718del	ENSP00000484935.2:n.2715_2718del
ENST00000504915.3:c.3104_3107del	ENSP00000473355.2:p.Asn1035MetfsTer4
ENST00000505350.2:c.*3056_*3059del	ENSP00000481752.1:n.*3056_*3059del
ENST00000507379.6:c.2996_2999del	ENSP00000423224.2:p.Asn999MetfsTer4
ENST00000509732.6:c.3050_3053del	ENSP00000426541.2:p.Asn1017MetfsTer4
ENST00000512211.7:c.3050_3053del	ENSP00000423828.3:p.Asn1017MetfsTer4
ENST00000257430.9:c.3050_3053del MANE Select	ENSP00000257430.4:p.Asn1017MetfsTer4
ENST00000257430.8:c.3050_3053del	ENSP00000257430.4:p.Asn1017MetfsTer4
ENST00000502371.2:c.1403_1406del
ENST00000507379.5:c.2996_2999del	ENSP00000423224.1:p.Asn999MetfsTer4
ENST00000508376.6:c.3050_3053del	ENSP00000427089.2:p.Asn1017MetfsTer4
ENST00000508624.5:c.*2372_*2375del	ENSP00000424265.1:n.*2372_*2375del
ENST00000512211.6:c.3050_3053del	ENSP00000423828.2:p.Asn1017MetfsTer4
ENST00000520401.1:c.230+9672_230+9675del
NM_000038.5:c.3050_3053del	NP_000029.2:p.Asn1017MetfsTer4
NM_001127510.2:c.3050_3053del	NP_001120982.1:p.Asn1017MetfsTer4
NM_001127511.2:c.2996_2999del	NP_001120983.2:p.Asn999MetfsTer4
NM_001354895.1:c.3050_3053del	NP_001341824.1:p.Asn1017MetfsTer4
NM_001354896.1:c.3104_3107del	NP_001341825.1:p.Asn1035MetfsTer4
NM_001354897.1:c.3080_3083del	NP_001341826.1:p.Asn1027MetfsTer4
NM_001354898.1:c.2975_2978del	NP_001341827.1:p.Asn992MetfsTer4
NM_001354899.1:c.2966_2969del	NP_001341828.1:p.Asn989MetfsTer4
NM_001354900.1:c.2927_2930del	NP_001341829.1:p.Asn976MetfsTer4
NM_001354901.1:c.2873_2876del	NP_001341830.1:p.Asn958MetfsTer4
NM_001354902.1:c.2777_2780del	NP_001341831.1:p.Asn926MetfsTer4
NM_001354903.1:c.2747_2750del	NP_001341832.1:p.Asn916MetfsTer4
NM_001354904.1:c.2672_2675del	NP_001341833.1:p.Asn891MetfsTer4
NM_001354905.1:c.2570_2573del	NP_001341834.1:p.Asn857MetfsTer4
NM_001354906.1:c.2201_2204del	NP_001341835.1:p.Asn734MetfsTer4
NM_000038.6:c.3050_3053del MANE Select	NP_000029.2:p.Asn1017MetfsTer4
NM_001127510.3:c.3050_3053del	NP_001120982.1:p.Asn1017MetfsTer4
NM_001127511.3:c.2996_2999del	NP_001120983.2:p.Asn999MetfsTer4
NM_001354895.2:c.3050_3053del	NP_001341824.1:p.Asn1017MetfsTer4
NM_001354896.2:c.3104_3107del	NP_001341825.1:p.Asn1035MetfsTer4
NM_001354897.2:c.3080_3083del	NP_001341826.1:p.Asn1027MetfsTer4
NM_001354898.2:c.2975_2978del	NP_001341827.1:p.Asn992MetfsTer4
NM_001354899.2:c.2966_2969del	NP_001341828.1:p.Asn989MetfsTer4
NM_001354900.2:c.2927_2930del	NP_001341829.1:p.Asn976MetfsTer4
NM_001354901.2:c.2873_2876del	NP_001341830.1:p.Asn958MetfsTer4
NM_001354902.2:c.2777_2780del	NP_001341831.1:p.Asn926MetfsTer4
NM_001354903.2:c.2747_2750del	NP_001341832.1:p.Asn916MetfsTer4
NM_001354904.2:c.2672_2675del	NP_001341833.1:p.Asn891MetfsTer4
NM_001354905.2:c.2570_2573del	NP_001341834.1:p.Asn857MetfsTer4
NM_001354906.2:c.2201_2204del	NP_001341835.1:p.Asn734MetfsTer4