Canonical Allele Identifier: CA645372778

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837568_112837569del , CM000667.2:g.112837568_112837569del	GRCh38
NC_000005.9:g.112173265_112173266del , CM000667.1:g.112173265_112173266del	GRCh37
NC_000005.8:g.112201164_112201165del	NCBI36
NG_008481.4:g.150048_150049del , LRG_130:g.150048_150049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1639_1640del	ENSP00000484935.2:n.1639_1640del
ENST00000504915.3:c.2028_2029del	ENSP00000473355.2:p.Asn677GlnfsTer14
ENST00000505350.2:c.*1980_*1981del	ENSP00000481752.1:n.*1980_*1981del
ENST00000507379.6:c.1920_1921del	ENSP00000423224.2:p.Asn641GlnfsTer14
ENST00000509732.6:c.1974_1975del	ENSP00000426541.2:p.Asn659GlnfsTer14
ENST00000512211.7:c.1974_1975del	ENSP00000423828.3:p.Asn659GlnfsTer14
ENST00000257430.9:c.1974_1975del MANE Select	ENSP00000257430.4:p.Asn659GlnfsTer14
ENST00000257430.8:c.1974_1975del	ENSP00000257430.4:p.Asn659GlnfsTer14
ENST00000502371.2:c.327_328del
ENST00000504915.2:c.663_664del	ENSP00000473355.1:p.Asn222GlnfsTer14
ENST00000507379.5:c.1920_1921del	ENSP00000423224.1:p.Asn641GlnfsTer14
ENST00000508376.6:c.1974_1975del	ENSP00000427089.2:p.Asn659GlnfsTer14
ENST00000508624.5:c.*1296_*1297del	ENSP00000424265.1:n.*1296_*1297del
ENST00000512211.6:c.1974_1975del	ENSP00000423828.2:p.Asn659GlnfsTer14
ENST00000520401.1:c.230+8596_230+8597del
NM_000038.5:c.1974_1975del	NP_000029.2:p.Asn659GlnfsTer14
NM_001127510.2:c.1974_1975del	NP_001120982.1:p.Asn659GlnfsTer14
NM_001127511.2:c.1920_1921del	NP_001120983.2:p.Asn641GlnfsTer14
NM_001354895.1:c.1974_1975del	NP_001341824.1:p.Asn659GlnfsTer14
NM_001354896.1:c.2028_2029del	NP_001341825.1:p.Asn677GlnfsTer14
NM_001354897.1:c.2004_2005del	NP_001341826.1:p.Asn669GlnfsTer14
NM_001354898.1:c.1899_1900del	NP_001341827.1:p.Asn634GlnfsTer14
NM_001354899.1:c.1890_1891del	NP_001341828.1:p.Asn631GlnfsTer14
NM_001354900.1:c.1851_1852del	NP_001341829.1:p.Asn618GlnfsTer14
NM_001354901.1:c.1797_1798del	NP_001341830.1:p.Asn600GlnfsTer14
NM_001354902.1:c.1701_1702del	NP_001341831.1:p.Asn568GlnfsTer14
NM_001354903.1:c.1671_1672del	NP_001341832.1:p.Asn558GlnfsTer14
NM_001354904.1:c.1596_1597del	NP_001341833.1:p.Asn533GlnfsTer14
NM_001354905.1:c.1494_1495del	NP_001341834.1:p.Asn499GlnfsTer14
NM_001354906.1:c.1125_1126del	NP_001341835.1:p.Asn376GlnfsTer14
NM_000038.6:c.1974_1975del MANE Select	NP_000029.2:p.Asn659GlnfsTer14
NM_001127510.3:c.1974_1975del	NP_001120982.1:p.Asn659GlnfsTer14
NM_001127511.3:c.1920_1921del	NP_001120983.2:p.Asn641GlnfsTer14
NM_001354895.2:c.1974_1975del	NP_001341824.1:p.Asn659GlnfsTer14
NM_001354896.2:c.2028_2029del	NP_001341825.1:p.Asn677GlnfsTer14
NM_001354897.2:c.2004_2005del	NP_001341826.1:p.Asn669GlnfsTer14
NM_001354898.2:c.1899_1900del	NP_001341827.1:p.Asn634GlnfsTer14
NM_001354899.2:c.1890_1891del	NP_001341828.1:p.Asn631GlnfsTer14
NM_001354900.2:c.1851_1852del	NP_001341829.1:p.Asn618GlnfsTer14
NM_001354901.2:c.1797_1798del	NP_001341830.1:p.Asn600GlnfsTer14
NM_001354902.2:c.1701_1702del	NP_001341831.1:p.Asn568GlnfsTer14
NM_001354903.2:c.1671_1672del	NP_001341832.1:p.Asn558GlnfsTer14
NM_001354904.2:c.1596_1597del	NP_001341833.1:p.Asn533GlnfsTer14
NM_001354905.2:c.1494_1495del	NP_001341834.1:p.Asn499GlnfsTer14
NM_001354906.2:c.1125_1126del	NP_001341835.1:p.Asn376GlnfsTer14