Canonical Allele Identifier: CA2740097766

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840620_112840628delinsGGAGGAGGA , CM000667.2:g.112840620_112840628delinsGGAGGAGGA	GRCh38
NC_000005.9:g.112176317_112176325delinsGGAGGAGGA , CM000667.1:g.112176317_112176325delinsGGAGGAGGA	GRCh37
NC_000005.8:g.112204216_112204224delinsGGAGGAGGA	NCBI36
NG_008481.4:g.153100_153108delinsGGAGGAGGA , LRG_130:g.153100_153108delinsGGAGGAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5080_5088delinsGGAGGAGGA	ENSP00000473355.2:p.Arg1694Gly
ENST00000505350.2:c.*5032_*5040delinsGGAGGAGGA	ENSP00000481752.1:n.*5032_*5040delinsGGAGGAGGA
ENST00000507379.6:c.4972_4980delinsGGAGGAGGA	ENSP00000423224.2:p.Arg1658Gly
ENST00000509732.6:c.5026_5034delinsGGAGGAGGA	ENSP00000426541.2:p.Arg1676Gly
ENST00000512211.7:c.5026_5034delinsGGAGGAGGA	ENSP00000423828.3:p.Arg1676Gly
ENST00000257430.9:c.5026_5034delinsGGAGGAGGA MANE Select	ENSP00000257430.4:p.Arg1676Gly
ENST00000257430.8:c.5026_5034delinsGGAGGAGGA	ENSP00000257430.4:p.Arg1676Gly
ENST00000508376.6:c.5026_5034delinsGGAGGAGGA	ENSP00000427089.2:p.Arg1676Gly
ENST00000508624.5:c.*4348_*4356delinsGGAGGAGGA	ENSP00000424265.1:n.*4348_*4356delinsGGAGGAGGA
ENST00000520401.1:c.230+11648_230+11656delinsGGAGGAGGA
NM_000038.5:c.5026_5034delinsGGAGGAGGA	NP_000029.2:p.Arg1676Gly
NM_001127510.2:c.5026_5034delinsGGAGGAGGA	NP_001120982.1:p.Arg1676Gly
NM_001127511.2:c.4972_4980delinsGGAGGAGGA	NP_001120983.2:p.Arg1658Gly
NM_001354895.1:c.5026_5034delinsGGAGGAGGA	NP_001341824.1:p.Arg1676Gly
NM_001354896.1:c.5080_5088delinsGGAGGAGGA	NP_001341825.1:p.Arg1694Gly
NM_001354897.1:c.5056_5064delinsGGAGGAGGA	NP_001341826.1:p.Arg1686Gly
NM_001354898.1:c.4951_4959delinsGGAGGAGGA	NP_001341827.1:p.Arg1651Gly
NM_001354899.1:c.4942_4950delinsGGAGGAGGA	NP_001341828.1:p.Arg1648Gly
NM_001354900.1:c.4903_4911delinsGGAGGAGGA	NP_001341829.1:p.Arg1635Gly
NM_001354901.1:c.4849_4857delinsGGAGGAGGA	NP_001341830.1:p.Arg1617Gly
NM_001354902.1:c.4753_4761delinsGGAGGAGGA	NP_001341831.1:p.Arg1585Gly
NM_001354903.1:c.4723_4731delinsGGAGGAGGA	NP_001341832.1:p.Arg1575Gly
NM_001354904.1:c.4648_4656delinsGGAGGAGGA	NP_001341833.1:p.Arg1550Gly
NM_001354905.1:c.4546_4554delinsGGAGGAGGA	NP_001341834.1:p.Arg1516Gly
NM_001354906.1:c.4177_4185delinsGGAGGAGGA	NP_001341835.1:p.Arg1393Gly
NM_000038.6:c.5026_5034delinsGGAGGAGGA MANE Select	NP_000029.2:p.Arg1676Gly
NM_001127510.3:c.5026_5034delinsGGAGGAGGA	NP_001120982.1:p.Arg1676Gly
NM_001127511.3:c.4972_4980delinsGGAGGAGGA	NP_001120983.2:p.Arg1658Gly
NM_001354895.2:c.5026_5034delinsGGAGGAGGA	NP_001341824.1:p.Arg1676Gly
NM_001354896.2:c.5080_5088delinsGGAGGAGGA	NP_001341825.1:p.Arg1694Gly
NM_001354897.2:c.5056_5064delinsGGAGGAGGA	NP_001341826.1:p.Arg1686Gly
NM_001354898.2:c.4951_4959delinsGGAGGAGGA	NP_001341827.1:p.Arg1651Gly
NM_001354899.2:c.4942_4950delinsGGAGGAGGA	NP_001341828.1:p.Arg1648Gly
NM_001354900.2:c.4903_4911delinsGGAGGAGGA	NP_001341829.1:p.Arg1635Gly
NM_001354901.2:c.4849_4857delinsGGAGGAGGA	NP_001341830.1:p.Arg1617Gly
NM_001354902.2:c.4753_4761delinsGGAGGAGGA	NP_001341831.1:p.Arg1585Gly
NM_001354903.2:c.4723_4731delinsGGAGGAGGA	NP_001341832.1:p.Arg1575Gly
NM_001354904.2:c.4648_4656delinsGGAGGAGGA	NP_001341833.1:p.Arg1550Gly
NM_001354905.2:c.4546_4554delinsGGAGGAGGA	NP_001341834.1:p.Arg1516Gly
NM_001354906.2:c.4177_4185delinsGGAGGAGGA	NP_001341835.1:p.Arg1393Gly