Canonical Allele Identifier: CA445755729
Gene: APC HGNC NCBI

Linked Data

COSMIC: COSM19653
MyVariant Identifiers: chr5:g.112151279del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112815582del , CM000667.2:g.112815582del GRCh38
NC_000005.9:g.112151279del , CM000667.1:g.112151279del GRCh37
NC_000005.8:g.112179178del NCBI36
NG_008481.4:g.128062del , LRG_130:g.128062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.922del ENSP00000484935.2:p.Leu308TrpfsTer28
ENST00000504915.3:c.922del ENSP00000473355.2:p.Leu308TrpfsTer28
ENST00000505084.2:n.978del
ENST00000505350.2:c.*928del ENSP00000481752.1:n.*928del
ENST00000507379.6:c.868del ENSP00000423224.2:p.Leu290TrpfsTer28
ENST00000509732.6:c.922del ENSP00000426541.2:p.Leu308TrpfsTer28
ENST00000512211.7:c.922del ENSP00000423828.3:p.Leu308TrpfsTer28
ENST00000257430.9:c.922del MANE Select ENSP00000257430.4:p.Leu308TrpfsTer28
ENST00000257430.8:c.922del ENSP00000257430.4:p.Leu308TrpfsTer28
ENST00000507379.5:c.868del ENSP00000423224.1:p.Leu290TrpfsTer28
ENST00000508376.6:c.922del ENSP00000427089.2:p.Leu308TrpfsTer28
ENST00000508624.5:c.*244del ENSP00000424265.1:n.*244del
ENST00000512211.6:c.922del ENSP00000423828.2:p.Leu308TrpfsTer28
NM_000038.5:c.922del NP_000029.2:p.Leu308TrpfsTer28
NM_001127510.2:c.922del NP_001120982.1:p.Leu308TrpfsTer28
NM_001127511.2:c.868del NP_001120983.2:p.Leu290TrpfsTer28
NM_001354895.1:c.922del NP_001341824.1:p.Leu308TrpfsTer28
NM_001354896.1:c.922del NP_001341825.1:p.Leu308TrpfsTer28
NM_001354897.1:c.952del NP_001341826.1:p.Leu318TrpfsTer28
NM_001354898.1:c.847del NP_001341827.1:p.Leu283TrpfsTer28
NM_001354899.1:c.838del NP_001341828.1:p.Leu280TrpfsTer28
NM_001354900.1:c.745del NP_001341829.1:p.Leu249TrpfsTer28
NM_001354901.1:c.745del NP_001341830.1:p.Leu249TrpfsTer28
NM_001354902.1:c.952del NP_001341831.1:p.Leu318TrpfsTer?
NM_001354903.1:c.922del NP_001341832.1:p.Leu308TrpfsTer?
NM_001354904.1:c.847del NP_001341833.1:p.Leu283TrpfsTer?
NM_001354905.1:c.745del NP_001341834.1:p.Leu249TrpfsTer?
NM_001354906.1:c.73del NP_001341835.1:p.Leu25TrpfsTer28
NM_000038.6:c.922del MANE Select NP_000029.2:p.Leu308TrpfsTer28
NM_001127510.3:c.922del NP_001120982.1:p.Leu308TrpfsTer28
NM_001127511.3:c.868del NP_001120983.2:p.Leu290TrpfsTer28
NM_001354895.2:c.922del NP_001341824.1:p.Leu308TrpfsTer28
NM_001354896.2:c.922del NP_001341825.1:p.Leu308TrpfsTer28
NM_001354897.2:c.952del NP_001341826.1:p.Leu318TrpfsTer28
NM_001354898.2:c.847del NP_001341827.1:p.Leu283TrpfsTer28
NM_001354899.2:c.838del NP_001341828.1:p.Leu280TrpfsTer28
NM_001354900.2:c.745del NP_001341829.1:p.Leu249TrpfsTer28
NM_001354901.2:c.745del NP_001341830.1:p.Leu249TrpfsTer28
NM_001354902.2:c.952del NP_001341831.1:p.Leu318TrpfsTer?
NM_001354903.2:c.922del NP_001341832.1:p.Leu308TrpfsTer?
NM_001354904.2:c.847del NP_001341833.1:p.Leu283TrpfsTer?
NM_001354905.2:c.745del NP_001341834.1:p.Leu249TrpfsTer?
NM_001354906.2:c.73del NP_001341835.1:p.Leu25TrpfsTer28