Canonical Allele Identifier: CA658760930

Gene: APC

Linked Data

• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839109_112839110del , CM000667.2:g.112839109_112839110del	GRCh38
NC_000005.9:g.112174806_112174807del , CM000667.1:g.112174806_112174807del	GRCh37
NC_000005.8:g.112202705_112202706del	NCBI36
NG_008481.4:g.151589_151590del , LRG_130:g.151589_151590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3180_3181del	ENSP00000484935.2:n.3180_3181del
ENST00000504915.3:c.3569_3570del	ENSP00000473355.2:p.His1190ArgfsTer6
ENST00000505350.2:c.*3521_*3522del	ENSP00000481752.1:n.*3521_*3522del
ENST00000507379.6:c.3461_3462del	ENSP00000423224.2:p.His1154ArgfsTer6
ENST00000509732.6:c.3515_3516del	ENSP00000426541.2:p.His1172ArgfsTer6
ENST00000512211.7:c.3515_3516del	ENSP00000423828.3:p.His1172ArgfsTer6
ENST00000257430.9:c.3515_3516del MANE Select	ENSP00000257430.4:p.His1172ArgfsTer6
ENST00000257430.8:c.3515_3516del	ENSP00000257430.4:p.His1172ArgfsTer6
ENST00000502371.2:c.1868_1869del
ENST00000508376.6:c.3515_3516del	ENSP00000427089.2:p.His1172ArgfsTer6
ENST00000508624.5:c.*2837_*2838del	ENSP00000424265.1:n.*2837_*2838del
ENST00000512211.6:c.3515_3516del	ENSP00000423828.2:p.His1172ArgfsTer6
ENST00000520401.1:c.230+10137_230+10138del
NM_000038.5:c.3515_3516del	NP_000029.2:p.His1172ArgfsTer6
NM_001127510.2:c.3515_3516del	NP_001120982.1:p.His1172ArgfsTer6
NM_001127511.2:c.3461_3462del	NP_001120983.2:p.His1154ArgfsTer6
NM_001354895.1:c.3515_3516del	NP_001341824.1:p.His1172ArgfsTer6
NM_001354896.1:c.3569_3570del	NP_001341825.1:p.His1190ArgfsTer6
NM_001354897.1:c.3545_3546del	NP_001341826.1:p.His1182ArgfsTer6
NM_001354898.1:c.3440_3441del	NP_001341827.1:p.His1147ArgfsTer6
NM_001354899.1:c.3431_3432del	NP_001341828.1:p.His1144ArgfsTer6
NM_001354900.1:c.3392_3393del	NP_001341829.1:p.His1131ArgfsTer6
NM_001354901.1:c.3338_3339del	NP_001341830.1:p.His1113ArgfsTer6
NM_001354902.1:c.3242_3243del	NP_001341831.1:p.His1081ArgfsTer6
NM_001354903.1:c.3212_3213del	NP_001341832.1:p.His1071ArgfsTer6
NM_001354904.1:c.3137_3138del	NP_001341833.1:p.His1046ArgfsTer6
NM_001354905.1:c.3035_3036del	NP_001341834.1:p.His1012ArgfsTer6
NM_001354906.1:c.2666_2667del	NP_001341835.1:p.His889ArgfsTer6
NM_000038.6:c.3515_3516del MANE Select	NP_000029.2:p.His1172ArgfsTer6
NM_001127510.3:c.3515_3516del	NP_001120982.1:p.His1172ArgfsTer6
NM_001127511.3:c.3461_3462del	NP_001120983.2:p.His1154ArgfsTer6
NM_001354895.2:c.3515_3516del	NP_001341824.1:p.His1172ArgfsTer6
NM_001354896.2:c.3569_3570del	NP_001341825.1:p.His1190ArgfsTer6
NM_001354897.2:c.3545_3546del	NP_001341826.1:p.His1182ArgfsTer6
NM_001354898.2:c.3440_3441del	NP_001341827.1:p.His1147ArgfsTer6
NM_001354899.2:c.3431_3432del	NP_001341828.1:p.His1144ArgfsTer6
NM_001354900.2:c.3392_3393del	NP_001341829.1:p.His1131ArgfsTer6
NM_001354901.2:c.3338_3339del	NP_001341830.1:p.His1113ArgfsTer6
NM_001354902.2:c.3242_3243del	NP_001341831.1:p.His1081ArgfsTer6
NM_001354903.2:c.3212_3213del	NP_001341832.1:p.His1071ArgfsTer6
NM_001354904.2:c.3137_3138del	NP_001341833.1:p.His1046ArgfsTer6
NM_001354905.2:c.3035_3036del	NP_001341834.1:p.His1012ArgfsTer6
NM_001354906.2:c.2666_2667del	NP_001341835.1:p.His889ArgfsTer6