Canonical Allele Identifier: CA658760442
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112801361del , CM000667.2:g.112801361del GRCh38
NC_000005.9:g.112137058del , CM000667.1:g.112137058del GRCh37
NC_000005.8:g.112164957del NCBI36
NG_008481.4:g.113841del , LRG_130:g.113841del

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.812del ENSP00000484935.2:p.Met271ArgfsTer22
ENST00000504915.3:c.812del ENSP00000473355.2:p.Met271ArgfsTer22
ENST00000505084.2:n.868del
ENST00000505350.2:c.*818del ENSP00000481752.1:n.*818del
ENST00000507379.6:c.758del ENSP00000423224.2:p.Met253ArgfsTer22
ENST00000509732.6:c.812del ENSP00000426541.2:p.Met271ArgfsTer22
ENST00000512211.7:c.812del ENSP00000423828.3:p.Met271ArgfsTer22
ENST00000257430.9:c.812del MANE Select ENSP00000257430.4:p.Met271ArgfsTer22
ENST00000257430.8:c.812del ENSP00000257430.4:p.Met271ArgfsTer22
ENST00000507379.5:c.758del ENSP00000423224.1:p.Met253ArgfsTer22
ENST00000508376.6:c.812del ENSP00000427089.2:p.Met271ArgfsTer22
ENST00000508624.5:c.812del ENSP00000424265.1:p.Met271ArgfsTer9
ENST00000512211.6:c.812del ENSP00000423828.2:p.Met271ArgfsTer22
NM_000038.5:c.812del NP_000029.2:p.Met271ArgfsTer22
NM_001127510.2:c.812del NP_001120982.1:p.Met271ArgfsTer22
NM_001127511.2:c.758del NP_001120983.2:p.Met253ArgfsTer22
NM_001354895.1:c.812del NP_001341824.1:p.Met271ArgfsTer22
NM_001354896.1:c.812del NP_001341825.1:p.Met271ArgfsTer22
NM_001354897.1:c.842del NP_001341826.1:p.Met281ArgfsTer22
NM_001354898.1:c.737del NP_001341827.1:p.Met246ArgfsTer22
NM_001354899.1:c.728del NP_001341828.1:p.Met243ArgfsTer22
NM_001354900.1:c.635del NP_001341829.1:p.Met212ArgfsTer22
NM_001354901.1:c.635del NP_001341830.1:p.Met212ArgfsTer22
NM_001354902.1:c.842del NP_001341831.1:p.Met281ArgfsTer22
NM_001354903.1:c.812del NP_001341832.1:p.Met271ArgfsTer22
NM_001354904.1:c.737del NP_001341833.1:p.Met246ArgfsTer22
NM_001354905.1:c.635del NP_001341834.1:p.Met212ArgfsTer22
NM_001354906.1:c.-224del NP_001341835.1:n.-224del
NM_000038.6:c.812del MANE Select NP_000029.2:p.Met271ArgfsTer22
NM_001127510.3:c.812del NP_001120982.1:p.Met271ArgfsTer22
NM_001127511.3:c.758del NP_001120983.2:p.Met253ArgfsTer22
NM_001354895.2:c.812del NP_001341824.1:p.Met271ArgfsTer22
NM_001354896.2:c.812del NP_001341825.1:p.Met271ArgfsTer22
NM_001354897.2:c.842del NP_001341826.1:p.Met281ArgfsTer22
NM_001354898.2:c.737del NP_001341827.1:p.Met246ArgfsTer22
NM_001354899.2:c.728del NP_001341828.1:p.Met243ArgfsTer22
NM_001354900.2:c.635del NP_001341829.1:p.Met212ArgfsTer22
NM_001354901.2:c.635del NP_001341830.1:p.Met212ArgfsTer22
NM_001354902.2:c.842del NP_001341831.1:p.Met281ArgfsTer22
NM_001354903.2:c.812del NP_001341832.1:p.Met271ArgfsTer22
NM_001354904.2:c.737del NP_001341833.1:p.Met246ArgfsTer22
NM_001354905.2:c.635del NP_001341834.1:p.Met212ArgfsTer22
NM_001354906.2:c.-224del NP_001341835.1:n.-224del