Canonical Allele Identifier: CA2580072370

Gene: APC

Linked Data

• ClinVar Variation Id: 1757197
• ClinVar RCV Id: RCV002367382

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842699_112842714delinsT , CM000667.2:g.112842699_112842714delinsT	GRCh38
NC_000005.9:g.112178396_112178411delinsT , CM000667.1:g.112178396_112178411delinsT	GRCh37
NC_000005.8:g.112206295_112206310delinsT	NCBI36
NG_008481.4:g.155179_155194delinsT , LRG_130:g.155179_155194delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7159_7174delinsT	ENSP00000473355.2:p.Pro2387_Ser2392delinsCys
ENST00000505350.2:c.*7111_*7126delinsT	ENSP00000481752.1:n.*7111_*7126delinsT
ENST00000507379.6:c.7051_7066delinsT	ENSP00000423224.2:p.Pro2351_Ser2356delinsCys
ENST00000509732.6:c.7105_7120delinsT	ENSP00000426541.2:p.Pro2369_Ser2374delinsCys
ENST00000512211.7:c.7105_7120delinsT	ENSP00000423828.3:p.Pro2369_Ser2374delinsCys
ENST00000257430.9:c.7105_7120delinsT MANE Select	ENSP00000257430.4:p.Pro2369_Ser2374delinsCys
ENST00000257430.8:c.7105_7120delinsT	ENSP00000257430.4:p.Pro2369_Ser2374delinsCys
ENST00000508376.6:c.7105_7120delinsT	ENSP00000427089.2:p.Pro2369_Ser2374delinsCys
ENST00000508624.5:c.*6427_*6442delinsT	ENSP00000424265.1:n.*6427_*6442delinsT
ENST00000520401.1:c.230+13727_230+13742delinsT
NM_000038.5:c.7105_7120delinsT	NP_000029.2:p.Pro2369_Ser2374delinsCys
NM_001127510.2:c.7105_7120delinsT	NP_001120982.1:p.Pro2369_Ser2374delinsCys
NM_001127511.2:c.7051_7066delinsT	NP_001120983.2:p.Pro2351_Ser2356delinsCys
NM_001354895.1:c.7105_7120delinsT	NP_001341824.1:p.Pro2369_Ser2374delinsCys
NM_001354896.1:c.7159_7174delinsT	NP_001341825.1:p.Pro2387_Ser2392delinsCys
NM_001354897.1:c.7135_7150delinsT	NP_001341826.1:p.Pro2379_Ser2384delinsCys
NM_001354898.1:c.7030_7045delinsT	NP_001341827.1:p.Pro2344_Ser2349delinsCys
NM_001354899.1:c.7021_7036delinsT	NP_001341828.1:p.Pro2341_Ser2346delinsCys
NM_001354900.1:c.6982_6997delinsT	NP_001341829.1:p.Pro2328_Ser2333delinsCys
NM_001354901.1:c.6928_6943delinsT	NP_001341830.1:p.Pro2310_Ser2315delinsCys
NM_001354902.1:c.6832_6847delinsT	NP_001341831.1:p.Pro2278_Ser2283delinsCys
NM_001354903.1:c.6802_6817delinsT	NP_001341832.1:p.Pro2268_Ser2273delinsCys
NM_001354904.1:c.6727_6742delinsT	NP_001341833.1:p.Pro2243_Ser2248delinsCys
NM_001354905.1:c.6625_6640delinsT	NP_001341834.1:p.Pro2209_Ser2214delinsCys
NM_001354906.1:c.6256_6271delinsT	NP_001341835.1:p.Pro2086_Ser2091delinsCys
NM_000038.6:c.7105_7120delinsT MANE Select	NP_000029.2:p.Pro2369_Ser2374delinsCys
NM_001127510.3:c.7105_7120delinsT	NP_001120982.1:p.Pro2369_Ser2374delinsCys
NM_001127511.3:c.7051_7066delinsT	NP_001120983.2:p.Pro2351_Ser2356delinsCys
NM_001354895.2:c.7105_7120delinsT	NP_001341824.1:p.Pro2369_Ser2374delinsCys
NM_001354896.2:c.7159_7174delinsT	NP_001341825.1:p.Pro2387_Ser2392delinsCys
NM_001354897.2:c.7135_7150delinsT	NP_001341826.1:p.Pro2379_Ser2384delinsCys
NM_001354898.2:c.7030_7045delinsT	NP_001341827.1:p.Pro2344_Ser2349delinsCys
NM_001354899.2:c.7021_7036delinsT	NP_001341828.1:p.Pro2341_Ser2346delinsCys
NM_001354900.2:c.6982_6997delinsT	NP_001341829.1:p.Pro2328_Ser2333delinsCys
NM_001354901.2:c.6928_6943delinsT	NP_001341830.1:p.Pro2310_Ser2315delinsCys
NM_001354902.2:c.6832_6847delinsT	NP_001341831.1:p.Pro2278_Ser2283delinsCys
NM_001354903.2:c.6802_6817delinsT	NP_001341832.1:p.Pro2268_Ser2273delinsCys
NM_001354904.2:c.6727_6742delinsT	NP_001341833.1:p.Pro2243_Ser2248delinsCys
NM_001354905.2:c.6625_6640delinsT	NP_001341834.1:p.Pro2209_Ser2214delinsCys
NM_001354906.2:c.6256_6271delinsT	NP_001341835.1:p.Pro2086_Ser2091delinsCys