Canonical Allele Identifier: CA1573505294
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112827162_112827175delinsTTACTAATGACCAC , CM000667.2:g.112827162_112827175delinsTTACTAATGACCAC GRCh38
NC_000005.9:g.112162859_112162872delinsTTACTAATGACCAC , CM000667.1:g.112162859_112162872delinsTTACTAATGACCAC GRCh37
NC_000005.8:g.112190758_112190771delinsTTACTAATGACCAC NCBI36
NG_008481.4:g.139642_139655delinsTTACTAATGACCAC , LRG_130:g.139642_139655delinsTTACTAATGACCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1408+5171_1408+5184delinsTTACTAATGACCAC ENSP00000484935.2:n.1408+5171_1408+5184de...
ENST00000504915.3:c.1517_1530delinsTTACTAATGACCAC ENSP00000473355.2:p.Leu506=
ENST00000505084.2:n.1519_1532delinsTTACTAATGACCAC
ENST00000505350.2:c.*1469_*1482delinsTTACTAATGACCAC ENSP00000481752.1:n.*1469_*1482delinsTTAC...
ENST00000507379.6:c.1409_1422delinsTTACTAATGACCAC ENSP00000423224.2:p.Leu470=
ENST00000509732.6:c.1463_1476delinsTTACTAATGACCAC ENSP00000426541.2:p.Leu488=
ENST00000512211.7:c.1463_1476delinsTTACTAATGACCAC ENSP00000423828.3:p.Leu488=
ENST00000257430.9:c.1463_1476delinsTTACTAATGACCAC MANE Select ENSP00000257430.4:p.Leu488=
ENST00000257430.8:c.1463_1476delinsTTACTAATGACCAC ENSP00000257430.4:p.Leu488=
ENST00000502371.2:c.96+5171_96+5184delinsTTACTAATGACCAC
ENST00000504915.2:c.152_165delinsTTACTAATGACCAC ENSP00000473355.1:p.Leu51=
ENST00000507379.5:c.1409_1422delinsTTACTAATGACCAC ENSP00000423224.1:p.Leu470=
ENST00000508376.6:c.1463_1476delinsTTACTAATGACCAC ENSP00000427089.2:p.Leu488=
ENST00000508624.5:c.*785_*798delinsTTACTAATGACCAC ENSP00000424265.1:n.*785_*798delinsTTACTA...
ENST00000512211.6:c.1463_1476delinsTTACTAATGACCAC ENSP00000423828.2:p.Leu488=
NM_000038.5:c.1463_1476delinsTTACTAATGACCAC NP_000029.2:p.Leu488=
NM_001127510.2:c.1463_1476delinsTTACTAATGACCAC NP_001120982.1:p.Leu488=
NM_001127511.2:c.1409_1422delinsTTACTAATGACCAC NP_001120983.2:p.Leu470=
NM_001354895.1:c.1463_1476delinsTTACTAATGACCAC NP_001341824.1:p.Leu488=
NM_001354896.1:c.1517_1530delinsTTACTAATGACCAC NP_001341825.1:p.Leu506=
NM_001354897.1:c.1493_1506delinsTTACTAATGACCAC NP_001341826.1:p.Leu498=
NM_001354898.1:c.1388_1401delinsTTACTAATGACCAC NP_001341827.1:p.Leu463=
NM_001354899.1:c.1379_1392delinsTTACTAATGACCAC NP_001341828.1:p.Leu460=
NM_001354900.1:c.1340_1353delinsTTACTAATGACCAC NP_001341829.1:p.Leu447=
NM_001354901.1:c.1286_1299delinsTTACTAATGACCAC NP_001341830.1:p.Leu429=
NM_001354902.1:c.1190_1203delinsTTACTAATGACCAC NP_001341831.1:p.Leu397=
NM_001354903.1:c.1160_1173delinsTTACTAATGACCAC NP_001341832.1:p.Leu387=
NM_001354904.1:c.1085_1098delinsTTACTAATGACCAC NP_001341833.1:p.Leu362=
NM_001354905.1:c.983_996delinsTTACTAATGACCAC NP_001341834.1:p.Leu328=
NM_001354906.1:c.614_627delinsTTACTAATGACCAC NP_001341835.1:p.Leu205=
NM_000038.6:c.1463_1476delinsTTACTAATGACCAC MANE Select NP_000029.2:p.Leu488=
NM_001127510.3:c.1463_1476delinsTTACTAATGACCAC NP_001120982.1:p.Leu488=
NM_001127511.3:c.1409_1422delinsTTACTAATGACCAC NP_001120983.2:p.Leu470=
NM_001354895.2:c.1463_1476delinsTTACTAATGACCAC NP_001341824.1:p.Leu488=
NM_001354896.2:c.1517_1530delinsTTACTAATGACCAC NP_001341825.1:p.Leu506=
NM_001354897.2:c.1493_1506delinsTTACTAATGACCAC NP_001341826.1:p.Leu498=
NM_001354898.2:c.1388_1401delinsTTACTAATGACCAC NP_001341827.1:p.Leu463=
NM_001354899.2:c.1379_1392delinsTTACTAATGACCAC NP_001341828.1:p.Leu460=
NM_001354900.2:c.1340_1353delinsTTACTAATGACCAC NP_001341829.1:p.Leu447=
NM_001354901.2:c.1286_1299delinsTTACTAATGACCAC NP_001341830.1:p.Leu429=
NM_001354902.2:c.1190_1203delinsTTACTAATGACCAC NP_001341831.1:p.Leu397=
NM_001354903.2:c.1160_1173delinsTTACTAATGACCAC NP_001341832.1:p.Leu387=
NM_001354904.2:c.1085_1098delinsTTACTAATGACCAC NP_001341833.1:p.Leu362=
NM_001354905.2:c.983_996delinsTTACTAATGACCAC NP_001341834.1:p.Leu328=
NM_001354906.2:c.614_627delinsTTACTAATGACCAC NP_001341835.1:p.Leu205=