Canonical Allele Identifier: CA1573471296

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835098_112835111delinsATTATTGAAAGTGG , CM000667.2:g.112835098_112835111delinsATTATTGAAAGTGG	GRCh38
NC_000005.9:g.112170795_112170808delinsATTATTGAAAGTGG , CM000667.1:g.112170795_112170808delinsATTATTGAAAGTGG	GRCh37
NC_000005.8:g.112198694_112198707delinsATTATTGAAAGTGG	NCBI36
NG_008481.4:g.147578_147591delinsATTATTGAAAGTGG , LRG_130:g.147578_147591delinsATTATTGAAAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1556_1569delinsATTATTGAAAGTGG	ENSP00000484935.2:n.1556_1569delinsATTATTGAAAGTGG
ENST00000504915.3:c.1945_1958delinsATTATTGAAAGTGG	ENSP00000473355.2:p.Ile649=
ENST00000505350.2:c.*1897_*1910delinsATTATTGAAAGTGG	ENSP00000481752.1:n.*1897_*1910delinsATTATTGAAAGTGG
ENST00000507379.6:c.1837_1850delinsATTATTGAAAGTGG	ENSP00000423224.2:p.Ile613=
ENST00000509732.6:c.1891_1904delinsATTATTGAAAGTGG	ENSP00000426541.2:p.Ile631=
ENST00000512211.7:c.1891_1904delinsATTATTGAAAGTGG	ENSP00000423828.3:p.Ile631=
ENST00000257430.9:c.1891_1904delinsATTATTGAAAGTGG MANE Select	ENSP00000257430.4:p.Ile631=
ENST00000257430.8:c.1891_1904delinsATTATTGAAAGTGG	ENSP00000257430.4:p.Ile631=
ENST00000502371.2:c.244_257delinsATTATTGAAAGTGG
ENST00000504915.2:c.580_593delinsATTATTGAAAGTGG	ENSP00000473355.1:p.Ile194=
ENST00000507379.5:c.1837_1850delinsATTATTGAAAGTGG	ENSP00000423224.1:p.Ile613=
ENST00000508376.6:c.1891_1904delinsATTATTGAAAGTGG	ENSP00000427089.2:p.Ile631=
ENST00000508624.5:c.*1213_*1226delinsATTATTGAAAGTGG	ENSP00000424265.1:n.*1213_*1226delinsATTATTGAAAGTGG
ENST00000512211.6:c.1891_1904delinsATTATTGAAAGTGG	ENSP00000423828.2:p.Ile631=
ENST00000520401.1:c.230+6126_230+6139delinsATTATTGAAAGTGG
NM_000038.5:c.1891_1904delinsATTATTGAAAGTGG	NP_000029.2:p.Ile631=
NM_001127510.2:c.1891_1904delinsATTATTGAAAGTGG	NP_001120982.1:p.Ile631=
NM_001127511.2:c.1837_1850delinsATTATTGAAAGTGG	NP_001120983.2:p.Ile613=
NM_001354895.1:c.1891_1904delinsATTATTGAAAGTGG	NP_001341824.1:p.Ile631=
NM_001354896.1:c.1945_1958delinsATTATTGAAAGTGG	NP_001341825.1:p.Ile649=
NM_001354897.1:c.1921_1934delinsATTATTGAAAGTGG	NP_001341826.1:p.Ile641=
NM_001354898.1:c.1816_1829delinsATTATTGAAAGTGG	NP_001341827.1:p.Ile606=
NM_001354899.1:c.1807_1820delinsATTATTGAAAGTGG	NP_001341828.1:p.Ile603=
NM_001354900.1:c.1768_1781delinsATTATTGAAAGTGG	NP_001341829.1:p.Ile590=
NM_001354901.1:c.1714_1727delinsATTATTGAAAGTGG	NP_001341830.1:p.Ile572=
NM_001354902.1:c.1618_1631delinsATTATTGAAAGTGG	NP_001341831.1:p.Ile540=
NM_001354903.1:c.1588_1601delinsATTATTGAAAGTGG	NP_001341832.1:p.Ile530=
NM_001354904.1:c.1513_1526delinsATTATTGAAAGTGG	NP_001341833.1:p.Ile505=
NM_001354905.1:c.1411_1424delinsATTATTGAAAGTGG	NP_001341834.1:p.Ile471=
NM_001354906.1:c.1042_1055delinsATTATTGAAAGTGG	NP_001341835.1:p.Ile348=
NM_000038.6:c.1891_1904delinsATTATTGAAAGTGG MANE Select	NP_000029.2:p.Ile631=
NM_001127510.3:c.1891_1904delinsATTATTGAAAGTGG	NP_001120982.1:p.Ile631=
NM_001127511.3:c.1837_1850delinsATTATTGAAAGTGG	NP_001120983.2:p.Ile613=
NM_001354895.2:c.1891_1904delinsATTATTGAAAGTGG	NP_001341824.1:p.Ile631=
NM_001354896.2:c.1945_1958delinsATTATTGAAAGTGG	NP_001341825.1:p.Ile649=
NM_001354897.2:c.1921_1934delinsATTATTGAAAGTGG	NP_001341826.1:p.Ile641=
NM_001354898.2:c.1816_1829delinsATTATTGAAAGTGG	NP_001341827.1:p.Ile606=
NM_001354899.2:c.1807_1820delinsATTATTGAAAGTGG	NP_001341828.1:p.Ile603=
NM_001354900.2:c.1768_1781delinsATTATTGAAAGTGG	NP_001341829.1:p.Ile590=
NM_001354901.2:c.1714_1727delinsATTATTGAAAGTGG	NP_001341830.1:p.Ile572=
NM_001354902.2:c.1618_1631delinsATTATTGAAAGTGG	NP_001341831.1:p.Ile540=
NM_001354903.2:c.1588_1601delinsATTATTGAAAGTGG	NP_001341832.1:p.Ile530=
NM_001354904.2:c.1513_1526delinsATTATTGAAAGTGG	NP_001341833.1:p.Ile505=
NM_001354905.2:c.1411_1424delinsATTATTGAAAGTGG	NP_001341834.1:p.Ile471=
NM_001354906.2:c.1042_1055delinsATTATTGAAAGTGG	NP_001341835.1:p.Ile348=