Canonical Allele Identifier: CA16042098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371858
dbSNP Id: rs1057517569

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112842390_112842404del , CM000667.2:g.112842390_112842404del GRCh38
NC_000005.9:g.112178087_112178101del , CM000667.1:g.112178087_112178101del GRCh37
NC_000005.8:g.112205986_112206000del NCBI36
NG_008481.4:g.154870_154884del , LRG_130:g.154870_154884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.6850_6864del ENSP00000473355.2:p.Thr2284_Ser2288del
ENST00000505350.2:c.*6802_*6816del ENSP00000481752.1:n.*6802_*6816del
ENST00000507379.6:c.6742_6756del ENSP00000423224.2:p.Thr2248_Ser2252del
ENST00000509732.6:c.6796_6810del ENSP00000426541.2:p.Thr2266_Ser2270del
ENST00000512211.7:c.6796_6810del ENSP00000423828.3:p.Thr2266_Ser2270del
ENST00000257430.9:c.6796_6810del MANE Select ENSP00000257430.4:p.Thr2266_Ser2270del
ENST00000257430.8:c.6796_6810del ENSP00000257430.4:p.Thr2266_Ser2270del
ENST00000508376.6:c.6796_6810del ENSP00000427089.2:p.Thr2266_Ser2270del
ENST00000508624.5:c.*6118_*6132del ENSP00000424265.1:n.*6118_*6132del
ENST00000520401.1:c.230+13418_230+13432del
NM_000038.5:c.6796_6810del NP_000029.2:p.Thr2266_Ser2270del
NM_001127510.2:c.6796_6810del NP_001120982.1:p.Thr2266_Ser2270del
NM_001127511.2:c.6742_6756del NP_001120983.2:p.Thr2248_Ser2252del
NM_001354895.1:c.6796_6810del NP_001341824.1:p.Thr2266_Ser2270del
NM_001354896.1:c.6850_6864del NP_001341825.1:p.Thr2284_Ser2288del
NM_001354897.1:c.6826_6840del NP_001341826.1:p.Thr2276_Ser2280del
NM_001354898.1:c.6721_6735del NP_001341827.1:p.Thr2241_Ser2245del
NM_001354899.1:c.6712_6726del NP_001341828.1:p.Thr2238_Ser2242del
NM_001354900.1:c.6673_6687del NP_001341829.1:p.Thr2225_Ser2229del
NM_001354901.1:c.6619_6633del NP_001341830.1:p.Thr2207_Ser2211del
NM_001354902.1:c.6523_6537del NP_001341831.1:p.Thr2175_Ser2179del
NM_001354903.1:c.6493_6507del NP_001341832.1:p.Thr2165_Ser2169del
NM_001354904.1:c.6418_6432del NP_001341833.1:p.Thr2140_Ser2144del
NM_001354905.1:c.6316_6330del NP_001341834.1:p.Thr2106_Ser2110del
NM_001354906.1:c.5947_5961del NP_001341835.1:p.Thr1983_Ser1987del
NM_000038.6:c.6796_6810del MANE Select NP_000029.2:p.Thr2266_Ser2270del
NM_001127510.3:c.6796_6810del NP_001120982.1:p.Thr2266_Ser2270del
NM_001127511.3:c.6742_6756del NP_001120983.2:p.Thr2248_Ser2252del
NM_001354895.2:c.6796_6810del NP_001341824.1:p.Thr2266_Ser2270del
NM_001354896.2:c.6850_6864del NP_001341825.1:p.Thr2284_Ser2288del
NM_001354897.2:c.6826_6840del NP_001341826.1:p.Thr2276_Ser2280del
NM_001354898.2:c.6721_6735del NP_001341827.1:p.Thr2241_Ser2245del
NM_001354899.2:c.6712_6726del NP_001341828.1:p.Thr2238_Ser2242del
NM_001354900.2:c.6673_6687del NP_001341829.1:p.Thr2225_Ser2229del
NM_001354901.2:c.6619_6633del NP_001341830.1:p.Thr2207_Ser2211del
NM_001354902.2:c.6523_6537del NP_001341831.1:p.Thr2175_Ser2179del
NM_001354903.2:c.6493_6507del NP_001341832.1:p.Thr2165_Ser2169del
NM_001354904.2:c.6418_6432del NP_001341833.1:p.Thr2140_Ser2144del
NM_001354905.2:c.6316_6330del NP_001341834.1:p.Thr2106_Ser2110del
NM_001354906.2:c.5947_5961del NP_001341835.1:p.Thr1983_Ser1987del