Canonical Allele Identifier: CA2582341376
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2583901
ClinVar RCV Id: RCV003337542

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840399del , CM000667.2:g.112840399del GRCh38
NC_000005.9:g.112176096del , CM000667.1:g.112176096del GRCh37
NC_000005.8:g.112203995del NCBI36
NG_008481.4:g.152879del , LRG_130:g.152879del

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.4859del ENSP00000473355.2:p.Pro1620LeufsTer?
ENST00000505350.2:c.*4811del ENSP00000481752.1:n.*4811del
ENST00000507379.6:c.4751del ENSP00000423224.2:p.Pro1584LeufsTer?
ENST00000509732.6:c.4805del ENSP00000426541.2:p.Pro1602LeufsTer?
ENST00000512211.7:c.4805del ENSP00000423828.3:p.Pro1602LeufsTer?
ENST00000257430.9:c.4805del MANE Select ENSP00000257430.4:p.Pro1602LeufsTer?
ENST00000257430.8:c.4805del ENSP00000257430.4:p.Pro1602LeufsTer?
ENST00000508376.6:c.4805del ENSP00000427089.2:p.Pro1602LeufsTer?
ENST00000508624.5:c.*4127del ENSP00000424265.1:n.*4127del
ENST00000520401.1:c.230+11427del
NM_000038.5:c.4805del NP_000029.2:p.Pro1602LeufsTer?
NM_001127510.2:c.4805del NP_001120982.1:p.Pro1602LeufsTer?
NM_001127511.2:c.4751del NP_001120983.2:p.Pro1584LeufsTer?
NM_001354895.1:c.4805del NP_001341824.1:p.Pro1602LeufsTer?
NM_001354896.1:c.4859del NP_001341825.1:p.Pro1620LeufsTer?
NM_001354897.1:c.4835del NP_001341826.1:p.Pro1612LeufsTer?
NM_001354898.1:c.4730del NP_001341827.1:p.Pro1577LeufsTer?
NM_001354899.1:c.4721del NP_001341828.1:p.Pro1574LeufsTer?
NM_001354900.1:c.4682del NP_001341829.1:p.Pro1561LeufsTer?
NM_001354901.1:c.4628del NP_001341830.1:p.Pro1543LeufsTer?
NM_001354902.1:c.4532del NP_001341831.1:p.Pro1511LeufsTer?
NM_001354903.1:c.4502del NP_001341832.1:p.Pro1501LeufsTer?
NM_001354904.1:c.4427del NP_001341833.1:p.Pro1476LeufsTer?
NM_001354905.1:c.4325del NP_001341834.1:p.Pro1442LeufsTer?
NM_001354906.1:c.3956del NP_001341835.1:p.Pro1319LeufsTer?
NM_000038.6:c.4805del MANE Select NP_000029.2:p.Pro1602LeufsTer?
NM_001127510.3:c.4805del NP_001120982.1:p.Pro1602LeufsTer?
NM_001127511.3:c.4751del NP_001120983.2:p.Pro1584LeufsTer?
NM_001354895.2:c.4805del NP_001341824.1:p.Pro1602LeufsTer?
NM_001354896.2:c.4859del NP_001341825.1:p.Pro1620LeufsTer?
NM_001354897.2:c.4835del NP_001341826.1:p.Pro1612LeufsTer?
NM_001354898.2:c.4730del NP_001341827.1:p.Pro1577LeufsTer?
NM_001354899.2:c.4721del NP_001341828.1:p.Pro1574LeufsTer?
NM_001354900.2:c.4682del NP_001341829.1:p.Pro1561LeufsTer?
NM_001354901.2:c.4628del NP_001341830.1:p.Pro1543LeufsTer?
NM_001354902.2:c.4532del NP_001341831.1:p.Pro1511LeufsTer?
NM_001354903.2:c.4502del NP_001341832.1:p.Pro1501LeufsTer?
NM_001354904.2:c.4427del NP_001341833.1:p.Pro1476LeufsTer?
NM_001354905.2:c.4325del NP_001341834.1:p.Pro1442LeufsTer?
NM_001354906.2:c.3956del NP_001341835.1:p.Pro1319LeufsTer?