Canonical Allele Identifier: CA645562812

Gene: APC

Linked Data

• COSMIC: COSM4662376

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835002del , CM000667.2:g.112835002del	GRCh38
NC_000005.9:g.112170699del , CM000667.1:g.112170699del	GRCh37
NC_000005.8:g.112198598del	NCBI36
NG_008481.4:g.147482del , LRG_130:g.147482del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1460del	ENSP00000484935.2:p.Leu487CysfsTer?
ENST00000504915.3:c.1849del	ENSP00000473355.2:p.Cys617AlafsTer11
ENST00000505350.2:c.*1801del	ENSP00000481752.1:n.*1801del
ENST00000507379.6:c.1741del	ENSP00000423224.2:p.Cys581AlafsTer11
ENST00000509732.6:c.1795del	ENSP00000426541.2:p.Cys599AlafsTer11
ENST00000512211.7:c.1795del	ENSP00000423828.3:p.Cys599AlafsTer11
ENST00000257430.9:c.1795del MANE Select	ENSP00000257430.4:p.Cys599AlafsTer11
ENST00000257430.8:c.1795del	ENSP00000257430.4:p.Cys599AlafsTer11
ENST00000502371.2:c.148del
ENST00000504915.2:c.484del	ENSP00000473355.1:p.Cys162AlafsTer11
ENST00000507379.5:c.1741del	ENSP00000423224.1:p.Cys581AlafsTer11
ENST00000508376.6:c.1795del	ENSP00000427089.2:p.Cys599AlafsTer11
ENST00000508624.5:c.*1117del	ENSP00000424265.1:n.*1117del
ENST00000512211.6:c.1795del	ENSP00000423828.2:p.Cys599AlafsTer11
ENST00000520401.1:c.230+6030del
NM_000038.5:c.1795del	NP_000029.2:p.Cys599AlafsTer11
NM_001127510.2:c.1795del	NP_001120982.1:p.Cys599AlafsTer11
NM_001127511.2:c.1741del	NP_001120983.2:p.Cys581AlafsTer11
NM_001354895.1:c.1795del	NP_001341824.1:p.Cys599AlafsTer11
NM_001354896.1:c.1849del	NP_001341825.1:p.Cys617AlafsTer11
NM_001354897.1:c.1825del	NP_001341826.1:p.Cys609AlafsTer11
NM_001354898.1:c.1720del	NP_001341827.1:p.Cys574AlafsTer11
NM_001354899.1:c.1711del	NP_001341828.1:p.Cys571AlafsTer11
NM_001354900.1:c.1672del	NP_001341829.1:p.Cys558AlafsTer11
NM_001354901.1:c.1618del	NP_001341830.1:p.Cys540AlafsTer11
NM_001354902.1:c.1522del	NP_001341831.1:p.Cys508AlafsTer11
NM_001354903.1:c.1492del	NP_001341832.1:p.Cys498AlafsTer11
NM_001354904.1:c.1417del	NP_001341833.1:p.Cys473AlafsTer11
NM_001354905.1:c.1315del	NP_001341834.1:p.Cys439AlafsTer11
NM_001354906.1:c.946del	NP_001341835.1:p.Cys316AlafsTer11
NM_000038.6:c.1795del MANE Select	NP_000029.2:p.Cys599AlafsTer11
NM_001127510.3:c.1795del	NP_001120982.1:p.Cys599AlafsTer11
NM_001127511.3:c.1741del	NP_001120983.2:p.Cys581AlafsTer11
NM_001354895.2:c.1795del	NP_001341824.1:p.Cys599AlafsTer11
NM_001354896.2:c.1849del	NP_001341825.1:p.Cys617AlafsTer11
NM_001354897.2:c.1825del	NP_001341826.1:p.Cys609AlafsTer11
NM_001354898.2:c.1720del	NP_001341827.1:p.Cys574AlafsTer11
NM_001354899.2:c.1711del	NP_001341828.1:p.Cys571AlafsTer11
NM_001354900.2:c.1672del	NP_001341829.1:p.Cys558AlafsTer11
NM_001354901.2:c.1618del	NP_001341830.1:p.Cys540AlafsTer11
NM_001354902.2:c.1522del	NP_001341831.1:p.Cys508AlafsTer11
NM_001354903.2:c.1492del	NP_001341832.1:p.Cys498AlafsTer11
NM_001354904.2:c.1417del	NP_001341833.1:p.Cys473AlafsTer11
NM_001354905.2:c.1315del	NP_001341834.1:p.Cys439AlafsTer11
NM_001354906.2:c.946del	NP_001341835.1:p.Cys316AlafsTer11