Canonical Allele Identifier: CA1573466799
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112842698_112842701delinsTCCA , CM000667.2:g.112842698_112842701delinsTCCA GRCh38
NC_000005.9:g.112178395_112178398delinsTCCA , CM000667.1:g.112178395_112178398delinsTCCA GRCh37
NC_000005.8:g.112206294_112206297delinsTCCA NCBI36
NG_008481.4:g.155178_155181delinsTCCA , LRG_130:g.155178_155181delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7158_7161delinsTCCA ENSP00000473355.2:p.Ser2386=
ENST00000505350.2:c.*7110_*7113delinsTCCA ENSP00000481752.1:n.*7110_*7113delinsTCCA
ENST00000507379.6:c.7050_7053delinsTCCA ENSP00000423224.2:p.Ser2350=
ENST00000509732.6:c.7104_7107delinsTCCA ENSP00000426541.2:p.Ser2368=
ENST00000512211.7:c.7104_7107delinsTCCA ENSP00000423828.3:p.Ser2368=
ENST00000257430.9:c.7104_7107delinsTCCA MANE Select ENSP00000257430.4:p.Ser2368=
ENST00000257430.8:c.7104_7107delinsTCCA ENSP00000257430.4:p.Ser2368=
ENST00000508376.6:c.7104_7107delinsTCCA ENSP00000427089.2:p.Ser2368=
ENST00000508624.5:c.*6426_*6429delinsTCCA ENSP00000424265.1:n.*6426_*6429delinsTCCA
ENST00000520401.1:c.230+13726_230+13729delinsTCCA
NM_000038.5:c.7104_7107delinsTCCA NP_000029.2:p.Ser2368=
NM_001127510.2:c.7104_7107delinsTCCA NP_001120982.1:p.Ser2368=
NM_001127511.2:c.7050_7053delinsTCCA NP_001120983.2:p.Ser2350=
NM_001354895.1:c.7104_7107delinsTCCA NP_001341824.1:p.Ser2368=
NM_001354896.1:c.7158_7161delinsTCCA NP_001341825.1:p.Ser2386=
NM_001354897.1:c.7134_7137delinsTCCA NP_001341826.1:p.Ser2378=
NM_001354898.1:c.7029_7032delinsTCCA NP_001341827.1:p.Ser2343=
NM_001354899.1:c.7020_7023delinsTCCA NP_001341828.1:p.Ser2340=
NM_001354900.1:c.6981_6984delinsTCCA NP_001341829.1:p.Ser2327=
NM_001354901.1:c.6927_6930delinsTCCA NP_001341830.1:p.Ser2309=
NM_001354902.1:c.6831_6834delinsTCCA NP_001341831.1:p.Ser2277=
NM_001354903.1:c.6801_6804delinsTCCA NP_001341832.1:p.Ser2267=
NM_001354904.1:c.6726_6729delinsTCCA NP_001341833.1:p.Ser2242=
NM_001354905.1:c.6624_6627delinsTCCA NP_001341834.1:p.Ser2208=
NM_001354906.1:c.6255_6258delinsTCCA NP_001341835.1:p.Ser2085=
NM_000038.6:c.7104_7107delinsTCCA MANE Select NP_000029.2:p.Ser2368=
NM_001127510.3:c.7104_7107delinsTCCA NP_001120982.1:p.Ser2368=
NM_001127511.3:c.7050_7053delinsTCCA NP_001120983.2:p.Ser2350=
NM_001354895.2:c.7104_7107delinsTCCA NP_001341824.1:p.Ser2368=
NM_001354896.2:c.7158_7161delinsTCCA NP_001341825.1:p.Ser2386=
NM_001354897.2:c.7134_7137delinsTCCA NP_001341826.1:p.Ser2378=
NM_001354898.2:c.7029_7032delinsTCCA NP_001341827.1:p.Ser2343=
NM_001354899.2:c.7020_7023delinsTCCA NP_001341828.1:p.Ser2340=
NM_001354900.2:c.6981_6984delinsTCCA NP_001341829.1:p.Ser2327=
NM_001354901.2:c.6927_6930delinsTCCA NP_001341830.1:p.Ser2309=
NM_001354902.2:c.6831_6834delinsTCCA NP_001341831.1:p.Ser2277=
NM_001354903.2:c.6801_6804delinsTCCA NP_001341832.1:p.Ser2267=
NM_001354904.2:c.6726_6729delinsTCCA NP_001341833.1:p.Ser2242=
NM_001354905.2:c.6624_6627delinsTCCA NP_001341834.1:p.Ser2208=
NM_001354906.2:c.6255_6258delinsTCCA NP_001341835.1:p.Ser2085=