Canonical Allele Identifier: CA445758857

Gene: APC

Linked Data

• COSMIC: COSM19655
• MyVariant Identifiers: chr5:g.112170725del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835028del , CM000667.2:g.112835028del	GRCh38
NC_000005.9:g.112170725del , CM000667.1:g.112170725del	GRCh37
NC_000005.8:g.112198624del	NCBI36
NG_008481.4:g.147508del , LRG_130:g.147508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1486del	ENSP00000484935.2:n.1486del
ENST00000504915.3:c.1875del	ENSP00000473355.2:p.Cys625TrpfsTer3
ENST00000505350.2:c.*1827del	ENSP00000481752.1:n.*1827del
ENST00000507379.6:c.1767del	ENSP00000423224.2:p.Cys589TrpfsTer3
ENST00000509732.6:c.1821del	ENSP00000426541.2:p.Cys607TrpfsTer3
ENST00000512211.7:c.1821del	ENSP00000423828.3:p.Cys607TrpfsTer3
ENST00000257430.9:c.1821del MANE Select	ENSP00000257430.4:p.Cys607TrpfsTer3
ENST00000257430.8:c.1821del	ENSP00000257430.4:p.Cys607TrpfsTer3
ENST00000502371.2:c.174del
ENST00000504915.2:c.510del	ENSP00000473355.1:p.Cys170TrpfsTer3
ENST00000507379.5:c.1767del	ENSP00000423224.1:p.Cys589TrpfsTer3
ENST00000508376.6:c.1821del	ENSP00000427089.2:p.Cys607TrpfsTer3
ENST00000508624.5:c.*1143del	ENSP00000424265.1:n.*1143del
ENST00000512211.6:c.1821del	ENSP00000423828.2:p.Cys607TrpfsTer3
ENST00000520401.1:c.230+6056del
NM_000038.5:c.1821del	NP_000029.2:p.Cys607TrpfsTer3
NM_001127510.2:c.1821del	NP_001120982.1:p.Cys607TrpfsTer3
NM_001127511.2:c.1767del	NP_001120983.2:p.Cys589TrpfsTer3
NM_001354895.1:c.1821del	NP_001341824.1:p.Cys607TrpfsTer3
NM_001354896.1:c.1875del	NP_001341825.1:p.Cys625TrpfsTer3
NM_001354897.1:c.1851del	NP_001341826.1:p.Cys617TrpfsTer3
NM_001354898.1:c.1746del	NP_001341827.1:p.Cys582TrpfsTer3
NM_001354899.1:c.1737del	NP_001341828.1:p.Cys579TrpfsTer3
NM_001354900.1:c.1698del	NP_001341829.1:p.Cys566TrpfsTer3
NM_001354901.1:c.1644del	NP_001341830.1:p.Cys548TrpfsTer3
NM_001354902.1:c.1548del	NP_001341831.1:p.Cys516TrpfsTer3
NM_001354903.1:c.1518del	NP_001341832.1:p.Cys506TrpfsTer3
NM_001354904.1:c.1443del	NP_001341833.1:p.Cys481TrpfsTer3
NM_001354905.1:c.1341del	NP_001341834.1:p.Cys447TrpfsTer3
NM_001354906.1:c.972del	NP_001341835.1:p.Cys324TrpfsTer3
NM_000038.6:c.1821del MANE Select	NP_000029.2:p.Cys607TrpfsTer3
NM_001127510.3:c.1821del	NP_001120982.1:p.Cys607TrpfsTer3
NM_001127511.3:c.1767del	NP_001120983.2:p.Cys589TrpfsTer3
NM_001354895.2:c.1821del	NP_001341824.1:p.Cys607TrpfsTer3
NM_001354896.2:c.1875del	NP_001341825.1:p.Cys625TrpfsTer3
NM_001354897.2:c.1851del	NP_001341826.1:p.Cys617TrpfsTer3
NM_001354898.2:c.1746del	NP_001341827.1:p.Cys582TrpfsTer3
NM_001354899.2:c.1737del	NP_001341828.1:p.Cys579TrpfsTer3
NM_001354900.2:c.1698del	NP_001341829.1:p.Cys566TrpfsTer3
NM_001354901.2:c.1644del	NP_001341830.1:p.Cys548TrpfsTer3
NM_001354902.2:c.1548del	NP_001341831.1:p.Cys516TrpfsTer3
NM_001354903.2:c.1518del	NP_001341832.1:p.Cys506TrpfsTer3
NM_001354904.2:c.1443del	NP_001341833.1:p.Cys481TrpfsTer3
NM_001354905.2:c.1341del	NP_001341834.1:p.Cys447TrpfsTer3
NM_001354906.2:c.972del	NP_001341835.1:p.Cys324TrpfsTer3