Canonical Allele Identifier: CA1573475346

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840884_112840888delinsCAGTT , CM000667.2:g.112840884_112840888delinsCAGTT	GRCh38
NC_000005.9:g.112176581_112176585delinsCAGTT , CM000667.1:g.112176581_112176585delinsCAGTT	GRCh37
NC_000005.8:g.112204480_112204484delinsCAGTT	NCBI36
NG_008481.4:g.153364_153368delinsCAGTT , LRG_130:g.153364_153368delinsCAGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5344_5348delinsCAGTT	ENSP00000473355.2:p.Gln1782=
ENST00000505350.2:c.*5296_*5300delinsCAGTT	ENSP00000481752.1:n.*5296_*5300delinsCAGT...
ENST00000507379.6:c.5236_5240delinsCAGTT	ENSP00000423224.2:p.Gln1746=
ENST00000509732.6:c.5290_5294delinsCAGTT	ENSP00000426541.2:p.Gln1764=
ENST00000512211.7:c.5290_5294delinsCAGTT	ENSP00000423828.3:p.Gln1764=
ENST00000257430.9:c.5290_5294delinsCAGTT MANE Select	ENSP00000257430.4:p.Gln1764=
ENST00000257430.8:c.5290_5294delinsCAGTT	ENSP00000257430.4:p.Gln1764=
ENST00000508376.6:c.5290_5294delinsCAGTT	ENSP00000427089.2:p.Gln1764=
ENST00000508624.5:c.*4612_*4616delinsCAGTT	ENSP00000424265.1:n.*4612_*4616delinsCAGT...
ENST00000520401.1:c.230+11912_230+11916delinsCAGTT
NM_000038.5:c.5290_5294delinsCAGTT	NP_000029.2:p.Gln1764=
NM_001127510.2:c.5290_5294delinsCAGTT	NP_001120982.1:p.Gln1764=
NM_001127511.2:c.5236_5240delinsCAGTT	NP_001120983.2:p.Gln1746=
NM_001354895.1:c.5290_5294delinsCAGTT	NP_001341824.1:p.Gln1764=
NM_001354896.1:c.5344_5348delinsCAGTT	NP_001341825.1:p.Gln1782=
NM_001354897.1:c.5320_5324delinsCAGTT	NP_001341826.1:p.Gln1774=
NM_001354898.1:c.5215_5219delinsCAGTT	NP_001341827.1:p.Gln1739=
NM_001354899.1:c.5206_5210delinsCAGTT	NP_001341828.1:p.Gln1736=
NM_001354900.1:c.5167_5171delinsCAGTT	NP_001341829.1:p.Gln1723=
NM_001354901.1:c.5113_5117delinsCAGTT	NP_001341830.1:p.Gln1705=
NM_001354902.1:c.5017_5021delinsCAGTT	NP_001341831.1:p.Gln1673=
NM_001354903.1:c.4987_4991delinsCAGTT	NP_001341832.1:p.Gln1663=
NM_001354904.1:c.4912_4916delinsCAGTT	NP_001341833.1:p.Gln1638=
NM_001354905.1:c.4810_4814delinsCAGTT	NP_001341834.1:p.Gln1604=
NM_001354906.1:c.4441_4445delinsCAGTT	NP_001341835.1:p.Gln1481=
NM_000038.6:c.5290_5294delinsCAGTT MANE Select	NP_000029.2:p.Gln1764=
NM_001127510.3:c.5290_5294delinsCAGTT	NP_001120982.1:p.Gln1764=
NM_001127511.3:c.5236_5240delinsCAGTT	NP_001120983.2:p.Gln1746=
NM_001354895.2:c.5290_5294delinsCAGTT	NP_001341824.1:p.Gln1764=
NM_001354896.2:c.5344_5348delinsCAGTT	NP_001341825.1:p.Gln1782=
NM_001354897.2:c.5320_5324delinsCAGTT	NP_001341826.1:p.Gln1774=
NM_001354898.2:c.5215_5219delinsCAGTT	NP_001341827.1:p.Gln1739=
NM_001354899.2:c.5206_5210delinsCAGTT	NP_001341828.1:p.Gln1736=
NM_001354900.2:c.5167_5171delinsCAGTT	NP_001341829.1:p.Gln1723=
NM_001354901.2:c.5113_5117delinsCAGTT	NP_001341830.1:p.Gln1705=
NM_001354902.2:c.5017_5021delinsCAGTT	NP_001341831.1:p.Gln1673=
NM_001354903.2:c.4987_4991delinsCAGTT	NP_001341832.1:p.Gln1663=
NM_001354904.2:c.4912_4916delinsCAGTT	NP_001341833.1:p.Gln1638=
NM_001354905.2:c.4810_4814delinsCAGTT	NP_001341834.1:p.Gln1604=
NM_001354906.2:c.4441_4445delinsCAGTT	NP_001341835.1:p.Gln1481=