Canonical Allele Identifier: CA1573474325

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843470_112843486delinsACTTCTCAGACCGTTTC , CM000667.2:g.112843470_112843486delinsACTTCTCAGACCGTTTC	GRCh38
NC_000005.9:g.112179167_112179183delinsACTTCTCAGACCGTTTC , CM000667.1:g.112179167_112179183delinsACTTCTCAGACCGTTTC	GRCh37
NC_000005.8:g.112207066_112207082delinsACTTCTCAGACCGTTTC	NCBI36
NG_008481.4:g.155950_155966delinsACTTCTCAGACCGTTTC , LRG_130:g.155950_155966delinsACTTCTCAGACCGTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7930_7946delinsACTTCTCAGACCGTTTC	ENSP00000473355.2:p.Thr2644=
ENST00000505350.2:c.*7882_*7898delinsACTTCTCAGACCGTTTC	ENSP00000481752.1:n.*7882_*7898delinsACTTCTCAGACCGTTTC
ENST00000507379.6:c.7822_7838delinsACTTCTCAGACCGTTTC	ENSP00000423224.2:p.Thr2608=
ENST00000509732.6:c.7876_7892delinsACTTCTCAGACCGTTTC	ENSP00000426541.2:p.Thr2626=
ENST00000512211.7:c.7876_7892delinsACTTCTCAGACCGTTTC	ENSP00000423828.3:p.Thr2626=
ENST00000257430.9:c.7876_7892delinsACTTCTCAGACCGTTTC MANE Select	ENSP00000257430.4:p.Thr2626=
ENST00000257430.8:c.7876_7892delinsACTTCTCAGACCGTTTC	ENSP00000257430.4:p.Thr2626=
ENST00000508376.6:c.7876_7892delinsACTTCTCAGACCGTTTC	ENSP00000427089.2:p.Thr2626=
ENST00000520401.1:c.231-13179_231-13163delinsACTTCTCAGACCGTTTC
NM_000038.5:c.7876_7892delinsACTTCTCAGACCGTTTC	NP_000029.2:p.Thr2626=
NM_001127510.2:c.7876_7892delinsACTTCTCAGACCGTTTC	NP_001120982.1:p.Thr2626=
NM_001127511.2:c.7822_7838delinsACTTCTCAGACCGTTTC	NP_001120983.2:p.Thr2608=
NM_001354895.1:c.7876_7892delinsACTTCTCAGACCGTTTC	NP_001341824.1:p.Thr2626=
NM_001354896.1:c.7930_7946delinsACTTCTCAGACCGTTTC	NP_001341825.1:p.Thr2644=
NM_001354897.1:c.7906_7922delinsACTTCTCAGACCGTTTC	NP_001341826.1:p.Thr2636=
NM_001354898.1:c.7801_7817delinsACTTCTCAGACCGTTTC	NP_001341827.1:p.Thr2601=
NM_001354899.1:c.7792_7808delinsACTTCTCAGACCGTTTC	NP_001341828.1:p.Thr2598=
NM_001354900.1:c.7753_7769delinsACTTCTCAGACCGTTTC	NP_001341829.1:p.Thr2585=
NM_001354901.1:c.7699_7715delinsACTTCTCAGACCGTTTC	NP_001341830.1:p.Thr2567=
NM_001354902.1:c.7603_7619delinsACTTCTCAGACCGTTTC	NP_001341831.1:p.Thr2535=
NM_001354903.1:c.7573_7589delinsACTTCTCAGACCGTTTC	NP_001341832.1:p.Thr2525=
NM_001354904.1:c.7498_7514delinsACTTCTCAGACCGTTTC	NP_001341833.1:p.Thr2500=
NM_001354905.1:c.7396_7412delinsACTTCTCAGACCGTTTC	NP_001341834.1:p.Thr2466=
NM_001354906.1:c.7027_7043delinsACTTCTCAGACCGTTTC	NP_001341835.1:p.Thr2343=
NM_000038.6:c.7876_7892delinsACTTCTCAGACCGTTTC MANE Select	NP_000029.2:p.Thr2626=
NM_001127510.3:c.7876_7892delinsACTTCTCAGACCGTTTC	NP_001120982.1:p.Thr2626=
NM_001127511.3:c.7822_7838delinsACTTCTCAGACCGTTTC	NP_001120983.2:p.Thr2608=
NM_001354895.2:c.7876_7892delinsACTTCTCAGACCGTTTC	NP_001341824.1:p.Thr2626=
NM_001354896.2:c.7930_7946delinsACTTCTCAGACCGTTTC	NP_001341825.1:p.Thr2644=
NM_001354897.2:c.7906_7922delinsACTTCTCAGACCGTTTC	NP_001341826.1:p.Thr2636=
NM_001354898.2:c.7801_7817delinsACTTCTCAGACCGTTTC	NP_001341827.1:p.Thr2601=
NM_001354899.2:c.7792_7808delinsACTTCTCAGACCGTTTC	NP_001341828.1:p.Thr2598=
NM_001354900.2:c.7753_7769delinsACTTCTCAGACCGTTTC	NP_001341829.1:p.Thr2585=
NM_001354901.2:c.7699_7715delinsACTTCTCAGACCGTTTC	NP_001341830.1:p.Thr2567=
NM_001354902.2:c.7603_7619delinsACTTCTCAGACCGTTTC	NP_001341831.1:p.Thr2535=
NM_001354903.2:c.7573_7589delinsACTTCTCAGACCGTTTC	NP_001341832.1:p.Thr2525=
NM_001354904.2:c.7498_7514delinsACTTCTCAGACCGTTTC	NP_001341833.1:p.Thr2500=
NM_001354905.2:c.7396_7412delinsACTTCTCAGACCGTTTC	NP_001341834.1:p.Thr2466=
NM_001354906.2:c.7027_7043delinsACTTCTCAGACCGTTTC	NP_001341835.1:p.Thr2343=