Canonical Allele Identifier: CA915943469

Gene: APC

Linked Data

• ClinVar Variation Id: 822756
• ClinVar RCV Id: RCV001018374
• dbSNP Id: rs1580511959

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815541del , CM000667.2:g.112815541del	GRCh38
NC_000005.9:g.112151238del , CM000667.1:g.112151238del	GRCh37
NC_000005.8:g.112179137del	NCBI36
NG_008481.4:g.128021del , LRG_130:g.128021del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.881del	ENSP00000484935.2:p.Ser294LeufsTer11
ENST00000504915.3:c.881del	ENSP00000473355.2:p.Ser294LeufsTer11
ENST00000505084.2:n.937del
ENST00000505350.2:c.*887del	ENSP00000481752.1:n.*887del
ENST00000507379.6:c.827del	ENSP00000423224.2:p.Ser276LeufsTer11
ENST00000509732.6:c.881del	ENSP00000426541.2:p.Ser294LeufsTer11
ENST00000512211.7:c.881del	ENSP00000423828.3:p.Ser294LeufsTer11
ENST00000257430.9:c.881del MANE Select	ENSP00000257430.4:p.Ser294LeufsTer11
ENST00000257430.8:c.881del	ENSP00000257430.4:p.Ser294LeufsTer11
ENST00000507379.5:c.827del	ENSP00000423224.1:p.Ser276LeufsTer11
ENST00000508376.6:c.881del	ENSP00000427089.2:p.Ser294LeufsTer11
ENST00000508624.5:c.*203del	ENSP00000424265.1:n.*203del
ENST00000512211.6:c.881del	ENSP00000423828.2:p.Ser294LeufsTer11
NM_000038.5:c.881del	NP_000029.2:p.Ser294LeufsTer11
NM_001127510.2:c.881del	NP_001120982.1:p.Ser294LeufsTer11
NM_001127511.2:c.827del	NP_001120983.2:p.Ser276LeufsTer11
NM_001354895.1:c.881del	NP_001341824.1:p.Ser294LeufsTer11
NM_001354896.1:c.881del	NP_001341825.1:p.Ser294LeufsTer11
NM_001354897.1:c.911del	NP_001341826.1:p.Ser304LeufsTer11
NM_001354898.1:c.806del	NP_001341827.1:p.Ser269LeufsTer11
NM_001354899.1:c.797del	NP_001341828.1:p.Ser266LeufsTer11
NM_001354900.1:c.704del	NP_001341829.1:p.Ser235LeufsTer11
NM_001354901.1:c.704del	NP_001341830.1:p.Ser235LeufsTer11
NM_001354902.1:c.911del	NP_001341831.1:p.Ser304LeufsTer11
NM_001354903.1:c.881del	NP_001341832.1:p.Ser294LeufsTer11
NM_001354904.1:c.806del	NP_001341833.1:p.Ser269LeufsTer11
NM_001354905.1:c.704del	NP_001341834.1:p.Ser235LeufsTer11
NM_001354906.1:c.32del	NP_001341835.1:p.Ser11LeufsTer11
NM_000038.6:c.881del MANE Select	NP_000029.2:p.Ser294LeufsTer11
NM_001127510.3:c.881del	NP_001120982.1:p.Ser294LeufsTer11
NM_001127511.3:c.827del	NP_001120983.2:p.Ser276LeufsTer11
NM_001354895.2:c.881del	NP_001341824.1:p.Ser294LeufsTer11
NM_001354896.2:c.881del	NP_001341825.1:p.Ser294LeufsTer11
NM_001354897.2:c.911del	NP_001341826.1:p.Ser304LeufsTer11
NM_001354898.2:c.806del	NP_001341827.1:p.Ser269LeufsTer11
NM_001354899.2:c.797del	NP_001341828.1:p.Ser266LeufsTer11
NM_001354900.2:c.704del	NP_001341829.1:p.Ser235LeufsTer11
NM_001354901.2:c.704del	NP_001341830.1:p.Ser235LeufsTer11
NM_001354902.2:c.911del	NP_001341831.1:p.Ser304LeufsTer11
NM_001354903.2:c.881del	NP_001341832.1:p.Ser294LeufsTer11
NM_001354904.2:c.806del	NP_001341833.1:p.Ser269LeufsTer11
NM_001354905.2:c.704del	NP_001341834.1:p.Ser235LeufsTer11
NM_001354906.2:c.32del	NP_001341835.1:p.Ser11LeufsTer11