Canonical Allele Identifier: CA2695205041

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835012del , CM000667.2:g.112835012del	GRCh38
NC_000005.9:g.112170709del , CM000667.1:g.112170709del	GRCh37
NC_000005.8:g.112198608del	NCBI36
NG_008481.4:g.147492del , LRG_130:g.147492del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1470del	ENSP00000484935.2:n.1470del
ENST00000504915.3:c.1859del	ENSP00000473355.2:p.Asn620IlefsTer8
ENST00000505350.2:c.*1811del	ENSP00000481752.1:n.*1811del
ENST00000507379.6:c.1751del	ENSP00000423224.2:p.Asn584IlefsTer8
ENST00000509732.6:c.1805del	ENSP00000426541.2:p.Asn602IlefsTer8
ENST00000512211.7:c.1805del	ENSP00000423828.3:p.Asn602IlefsTer8
ENST00000257430.9:c.1805del MANE Select	ENSP00000257430.4:p.Asn602IlefsTer8
ENST00000257430.8:c.1805del	ENSP00000257430.4:p.Asn602IlefsTer8
ENST00000502371.2:c.158del
ENST00000504915.2:c.494del	ENSP00000473355.1:p.Asn165IlefsTer8
ENST00000507379.5:c.1751del	ENSP00000423224.1:p.Asn584IlefsTer8
ENST00000508376.6:c.1805del	ENSP00000427089.2:p.Asn602IlefsTer8
ENST00000508624.5:c.*1127del	ENSP00000424265.1:n.*1127del
ENST00000512211.6:c.1805del	ENSP00000423828.2:p.Asn602IlefsTer8
ENST00000520401.1:c.230+6040del
NM_000038.5:c.1805del	NP_000029.2:p.Asn602IlefsTer8
NM_001127510.2:c.1805del	NP_001120982.1:p.Asn602IlefsTer8
NM_001127511.2:c.1751del	NP_001120983.2:p.Asn584IlefsTer8
NM_001354895.1:c.1805del	NP_001341824.1:p.Asn602IlefsTer8
NM_001354896.1:c.1859del	NP_001341825.1:p.Asn620IlefsTer8
NM_001354897.1:c.1835del	NP_001341826.1:p.Asn612IlefsTer8
NM_001354898.1:c.1730del	NP_001341827.1:p.Asn577IlefsTer8
NM_001354899.1:c.1721del	NP_001341828.1:p.Asn574IlefsTer8
NM_001354900.1:c.1682del	NP_001341829.1:p.Asn561IlefsTer8
NM_001354901.1:c.1628del	NP_001341830.1:p.Asn543IlefsTer8
NM_001354902.1:c.1532del	NP_001341831.1:p.Asn511IlefsTer8
NM_001354903.1:c.1502del	NP_001341832.1:p.Asn501IlefsTer8
NM_001354904.1:c.1427del	NP_001341833.1:p.Asn476IlefsTer8
NM_001354905.1:c.1325del	NP_001341834.1:p.Asn442IlefsTer8
NM_001354906.1:c.956del	NP_001341835.1:p.Asn319IlefsTer8
NM_000038.6:c.1805del MANE Select	NP_000029.2:p.Asn602IlefsTer8
NM_001127510.3:c.1805del	NP_001120982.1:p.Asn602IlefsTer8
NM_001127511.3:c.1751del	NP_001120983.2:p.Asn584IlefsTer8
NM_001354895.2:c.1805del	NP_001341824.1:p.Asn602IlefsTer8
NM_001354896.2:c.1859del	NP_001341825.1:p.Asn620IlefsTer8
NM_001354897.2:c.1835del	NP_001341826.1:p.Asn612IlefsTer8
NM_001354898.2:c.1730del	NP_001341827.1:p.Asn577IlefsTer8
NM_001354899.2:c.1721del	NP_001341828.1:p.Asn574IlefsTer8
NM_001354900.2:c.1682del	NP_001341829.1:p.Asn561IlefsTer8
NM_001354901.2:c.1628del	NP_001341830.1:p.Asn543IlefsTer8
NM_001354902.2:c.1532del	NP_001341831.1:p.Asn511IlefsTer8
NM_001354903.2:c.1502del	NP_001341832.1:p.Asn501IlefsTer8
NM_001354904.2:c.1427del	NP_001341833.1:p.Asn476IlefsTer8
NM_001354905.2:c.1325del	NP_001341834.1:p.Asn442IlefsTer8
NM_001354906.2:c.956del	NP_001341835.1:p.Asn319IlefsTer8