Canonical Allele Identifier: CA279689

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837566_112837569del , CM000667.2:g.112837566_112837569del	GRCh38
NC_000005.9:g.112173263_112173266del , CM000667.1:g.112173263_112173266del	GRCh37
NC_000005.8:g.112201162_112201165del	NCBI36
NG_008481.4:g.150046_150049del , LRG_130:g.150046_150049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1637_1640del	ENSP00000484935.2:n.1637_1640del
ENST00000504915.3:c.2026_2029del	ENSP00000473355.2:p.Glu676ThrfsTer11
ENST00000505350.2:c.*1978_*1981del	ENSP00000481752.1:n.*1978_*1981del
ENST00000507379.6:c.1918_1921del	ENSP00000423224.2:p.Glu640ThrfsTer11
ENST00000509732.6:c.1972_1975del	ENSP00000426541.2:p.Glu658ThrfsTer11
ENST00000512211.7:c.1972_1975del	ENSP00000423828.3:p.Glu658ThrfsTer11
ENST00000257430.9:c.1972_1975del MANE Select	ENSP00000257430.4:p.Glu658ThrfsTer11
ENST00000257430.8:c.1972_1975del	ENSP00000257430.4:p.Glu658ThrfsTer11
ENST00000502371.2:c.325_328del
ENST00000504915.2:c.661_664del	ENSP00000473355.1:p.Glu221ThrfsTer11
ENST00000507379.5:c.1918_1921del	ENSP00000423224.1:p.Glu640ThrfsTer11
ENST00000508376.6:c.1972_1975del	ENSP00000427089.2:p.Glu658ThrfsTer11
ENST00000508624.5:c.*1294_*1297del	ENSP00000424265.1:n.*1294_*1297del
ENST00000512211.6:c.1972_1975del	ENSP00000423828.2:p.Glu658ThrfsTer11
ENST00000520401.1:c.230+8594_230+8597del
NM_000038.5:c.1972_1975del	NP_000029.2:p.Glu658ThrfsTer11
NM_001127510.2:c.1972_1975del	NP_001120982.1:p.Glu658ThrfsTer11
NM_001127511.2:c.1918_1921del	NP_001120983.2:p.Glu640ThrfsTer11
NM_001354895.1:c.1972_1975del	NP_001341824.1:p.Glu658ThrfsTer11
NM_001354896.1:c.2026_2029del	NP_001341825.1:p.Glu676ThrfsTer11
NM_001354897.1:c.2002_2005del	NP_001341826.1:p.Glu668ThrfsTer11
NM_001354898.1:c.1897_1900del	NP_001341827.1:p.Glu633ThrfsTer11
NM_001354899.1:c.1888_1891del	NP_001341828.1:p.Glu630ThrfsTer11
NM_001354900.1:c.1849_1852del	NP_001341829.1:p.Glu617ThrfsTer11
NM_001354901.1:c.1795_1798del	NP_001341830.1:p.Glu599ThrfsTer11
NM_001354902.1:c.1699_1702del	NP_001341831.1:p.Glu567ThrfsTer11
NM_001354903.1:c.1669_1672del	NP_001341832.1:p.Glu557ThrfsTer11
NM_001354904.1:c.1594_1597del	NP_001341833.1:p.Glu532ThrfsTer11
NM_001354905.1:c.1492_1495del	NP_001341834.1:p.Glu498ThrfsTer11
NM_001354906.1:c.1123_1126del	NP_001341835.1:p.Glu375ThrfsTer11
NM_000038.6:c.1972_1975del MANE Select	NP_000029.2:p.Glu658ThrfsTer11
NM_001127510.3:c.1972_1975del	NP_001120982.1:p.Glu658ThrfsTer11
NM_001127511.3:c.1918_1921del	NP_001120983.2:p.Glu640ThrfsTer11
NM_001354895.2:c.1972_1975del	NP_001341824.1:p.Glu658ThrfsTer11
NM_001354896.2:c.2026_2029del	NP_001341825.1:p.Glu676ThrfsTer11
NM_001354897.2:c.2002_2005del	NP_001341826.1:p.Glu668ThrfsTer11
NM_001354898.2:c.1897_1900del	NP_001341827.1:p.Glu633ThrfsTer11
NM_001354899.2:c.1888_1891del	NP_001341828.1:p.Glu630ThrfsTer11
NM_001354900.2:c.1849_1852del	NP_001341829.1:p.Glu617ThrfsTer11
NM_001354901.2:c.1795_1798del	NP_001341830.1:p.Glu599ThrfsTer11
NM_001354902.2:c.1699_1702del	NP_001341831.1:p.Glu567ThrfsTer11
NM_001354903.2:c.1669_1672del	NP_001341832.1:p.Glu557ThrfsTer11
NM_001354904.2:c.1594_1597del	NP_001341833.1:p.Glu532ThrfsTer11
NM_001354905.2:c.1492_1495del	NP_001341834.1:p.Glu498ThrfsTer11
NM_001354906.2:c.1123_1126del	NP_001341835.1:p.Glu375ThrfsTer11