Canonical Allele Identifier: CA2695205032

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828902del , CM000667.2:g.112828902del	GRCh38
NC_000005.9:g.112164599del , CM000667.1:g.112164599del	GRCh37
NC_000005.8:g.112192498del	NCBI36
NG_008481.4:g.141382del , LRG_130:g.141382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1409-6049del	ENSP00000484935.2:n.1409-6049del
ENST00000504915.3:c.1727del	ENSP00000473355.2:p.Asn576IlefsTer12
ENST00000505084.2:n.1729del
ENST00000505350.2:c.*1679del	ENSP00000481752.1:n.*1679del
ENST00000507379.6:c.1619del	ENSP00000423224.2:p.Asn540IlefsTer12
ENST00000509732.6:c.1673del	ENSP00000426541.2:p.Asn558IlefsTer12
ENST00000512211.7:c.1673del	ENSP00000423828.3:p.Asn558IlefsTer12
ENST00000257430.9:c.1673del MANE Select	ENSP00000257430.4:p.Asn558IlefsTer12
ENST00000257430.8:c.1673del	ENSP00000257430.4:p.Asn558IlefsTer12
ENST00000502371.2:c.97-6049del
ENST00000504915.2:c.362del	ENSP00000473355.1:p.Asn121IlefsTer12
ENST00000505084.1:n.160del
ENST00000507379.5:c.1619del	ENSP00000423224.1:p.Asn540IlefsTer12
ENST00000508376.6:c.1673del	ENSP00000427089.2:p.Asn558IlefsTer12
ENST00000508624.5:c.*995del	ENSP00000424265.1:n.*995del
ENST00000512211.6:c.1673del	ENSP00000423828.2:p.Asn558IlefsTer12
ENST00000520401.1:c.160del
NM_000038.5:c.1673del	NP_000029.2:p.Asn558IlefsTer12
NM_001127510.2:c.1673del	NP_001120982.1:p.Asn558IlefsTer12
NM_001127511.2:c.1619del	NP_001120983.2:p.Asn540IlefsTer12
NM_001354895.1:c.1673del	NP_001341824.1:p.Asn558IlefsTer12
NM_001354896.1:c.1727del	NP_001341825.1:p.Asn576IlefsTer12
NM_001354897.1:c.1703del	NP_001341826.1:p.Asn568IlefsTer12
NM_001354898.1:c.1598del	NP_001341827.1:p.Asn533IlefsTer12
NM_001354899.1:c.1589del	NP_001341828.1:p.Asn530IlefsTer12
NM_001354900.1:c.1550del	NP_001341829.1:p.Asn517IlefsTer12
NM_001354901.1:c.1496del	NP_001341830.1:p.Asn499IlefsTer12
NM_001354902.1:c.1400del	NP_001341831.1:p.Asn467IlefsTer12
NM_001354903.1:c.1370del	NP_001341832.1:p.Asn457IlefsTer12
NM_001354904.1:c.1295del	NP_001341833.1:p.Asn432IlefsTer12
NM_001354905.1:c.1193del	NP_001341834.1:p.Asn398IlefsTer12
NM_001354906.1:c.824del	NP_001341835.1:p.Asn275IlefsTer12
NM_000038.6:c.1673del MANE Select	NP_000029.2:p.Asn558IlefsTer12
NM_001127510.3:c.1673del	NP_001120982.1:p.Asn558IlefsTer12
NM_001127511.3:c.1619del	NP_001120983.2:p.Asn540IlefsTer12
NM_001354895.2:c.1673del	NP_001341824.1:p.Asn558IlefsTer12
NM_001354896.2:c.1727del	NP_001341825.1:p.Asn576IlefsTer12
NM_001354897.2:c.1703del	NP_001341826.1:p.Asn568IlefsTer12
NM_001354898.2:c.1598del	NP_001341827.1:p.Asn533IlefsTer12
NM_001354899.2:c.1589del	NP_001341828.1:p.Asn530IlefsTer12
NM_001354900.2:c.1550del	NP_001341829.1:p.Asn517IlefsTer12
NM_001354901.2:c.1496del	NP_001341830.1:p.Asn499IlefsTer12
NM_001354902.2:c.1400del	NP_001341831.1:p.Asn467IlefsTer12
NM_001354903.2:c.1370del	NP_001341832.1:p.Asn457IlefsTer12
NM_001354904.2:c.1295del	NP_001341833.1:p.Asn432IlefsTer12
NM_001354905.2:c.1193del	NP_001341834.1:p.Asn398IlefsTer12
NM_001354906.2:c.824del	NP_001341835.1:p.Asn275IlefsTer12