Canonical Allele Identifier: CA010446
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181835
dbSNP Id: rs730881273

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841084_112841087del , CM000667.2:g.112841084_112841087del GRCh38
NC_000005.9:g.112176781_112176784del , CM000667.1:g.112176781_112176784del GRCh37
NC_000005.8:g.112204680_112204683del NCBI36
NG_008481.4:g.153564_153567del , LRG_130:g.153564_153567del

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.5544_5547del ENSP00000473355.2:p.Asn1848LysfsTer?
ENST00000505350.2:c.*5496_*5499del ENSP00000481752.1:n.*5496_*5499del
ENST00000507379.6:c.5436_5439del ENSP00000423224.2:p.Asn1812LysfsTer?
ENST00000509732.6:c.5490_5493del ENSP00000426541.2:p.Asn1830LysfsTer?
ENST00000512211.7:c.5490_5493del ENSP00000423828.3:p.Asn1830LysfsTer?
ENST00000257430.9:c.5490_5493del MANE Select ENSP00000257430.4:p.Asn1830LysfsTer?
ENST00000257430.8:c.5490_5493del ENSP00000257430.4:p.Asn1830LysfsTer?
ENST00000508376.6:c.5490_5493del ENSP00000427089.2:p.Asn1830LysfsTer?
ENST00000508624.5:c.*4812_*4815del ENSP00000424265.1:n.*4812_*4815del
ENST00000520401.1:c.230+12112_230+12115del
NM_000038.5:c.5490_5493del NP_000029.2:p.Asn1830LysfsTer?
NM_001127510.2:c.5490_5493del NP_001120982.1:p.Asn1830LysfsTer?
NM_001127511.2:c.5436_5439del NP_001120983.2:p.Asn1812LysfsTer?
NM_001354895.1:c.5490_5493del NP_001341824.1:p.Asn1830LysfsTer?
NM_001354896.1:c.5544_5547del NP_001341825.1:p.Asn1848LysfsTer?
NM_001354897.1:c.5520_5523del NP_001341826.1:p.Asn1840LysfsTer?
NM_001354898.1:c.5415_5418del NP_001341827.1:p.Asn1805LysfsTer?
NM_001354899.1:c.5406_5409del NP_001341828.1:p.Asn1802LysfsTer?
NM_001354900.1:c.5367_5370del NP_001341829.1:p.Asn1789LysfsTer?
NM_001354901.1:c.5313_5316del NP_001341830.1:p.Asn1771LysfsTer?
NM_001354902.1:c.5217_5220del NP_001341831.1:p.Asn1739LysfsTer?
NM_001354903.1:c.5187_5190del NP_001341832.1:p.Asn1729LysfsTer?
NM_001354904.1:c.5112_5115del NP_001341833.1:p.Asn1704LysfsTer?
NM_001354905.1:c.5010_5013del NP_001341834.1:p.Asn1670LysfsTer?
NM_001354906.1:c.4641_4644del NP_001341835.1:p.Asn1547LysfsTer?
NM_000038.6:c.5490_5493del MANE Select NP_000029.2:p.Asn1830LysfsTer?
NM_001127510.3:c.5490_5493del NP_001120982.1:p.Asn1830LysfsTer?
NM_001127511.3:c.5436_5439del NP_001120983.2:p.Asn1812LysfsTer?
NM_001354895.2:c.5490_5493del NP_001341824.1:p.Asn1830LysfsTer?
NM_001354896.2:c.5544_5547del NP_001341825.1:p.Asn1848LysfsTer?
NM_001354897.2:c.5520_5523del NP_001341826.1:p.Asn1840LysfsTer?
NM_001354898.2:c.5415_5418del NP_001341827.1:p.Asn1805LysfsTer?
NM_001354899.2:c.5406_5409del NP_001341828.1:p.Asn1802LysfsTer?
NM_001354900.2:c.5367_5370del NP_001341829.1:p.Asn1789LysfsTer?
NM_001354901.2:c.5313_5316del NP_001341830.1:p.Asn1771LysfsTer?
NM_001354902.2:c.5217_5220del NP_001341831.1:p.Asn1739LysfsTer?
NM_001354903.2:c.5187_5190del NP_001341832.1:p.Asn1729LysfsTer?
NM_001354904.2:c.5112_5115del NP_001341833.1:p.Asn1704LysfsTer?
NM_001354905.2:c.5010_5013del NP_001341834.1:p.Asn1670LysfsTer?
NM_001354906.2:c.4641_4644del NP_001341835.1:p.Asn1547LysfsTer?