Canonical Allele Identifier: CA2767941967

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840557_112840558insACT , CM000667.2:g.112840557_112840558insACT	GRCh38
NC_000005.9:g.112176254_112176255insACT , CM000667.1:g.112176254_112176255insACT	GRCh37
NC_000005.8:g.112204153_112204154insACT	NCBI36
NG_008481.4:g.153037_153038insACT , LRG_130:g.153037_153038insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5017_5018insACT	ENSP00000473355.2:p.Thr1673delinsAsnSer
ENST00000505350.2:c.*4969_*4970insACT	ENSP00000481752.1:n.*4969_*4970insACT
ENST00000507379.6:c.4909_4910insACT	ENSP00000423224.2:p.Thr1637delinsAsnSer
ENST00000509732.6:c.4963_4964insACT	ENSP00000426541.2:p.Thr1655delinsAsnSer
ENST00000512211.7:c.4963_4964insACT	ENSP00000423828.3:p.Thr1655delinsAsnSer
ENST00000257430.9:c.4963_4964insACT MANE Select	ENSP00000257430.4:p.Thr1655delinsAsnSer
ENST00000257430.8:c.4963_4964insACT	ENSP00000257430.4:p.Thr1655delinsAsnSer
ENST00000508376.6:c.4963_4964insACT	ENSP00000427089.2:p.Thr1655delinsAsnSer
ENST00000508624.5:c.*4285_*4286insACT	ENSP00000424265.1:n.*4285_*4286insACT
ENST00000520401.1:c.230+11585_230+11586insACT
NM_000038.5:c.4963_4964insACT	NP_000029.2:p.Thr1655delinsAsnSer
NM_001127510.2:c.4963_4964insACT	NP_001120982.1:p.Thr1655delinsAsnSer
NM_001127511.2:c.4909_4910insACT	NP_001120983.2:p.Thr1637delinsAsnSer
NM_001354895.1:c.4963_4964insACT	NP_001341824.1:p.Thr1655delinsAsnSer
NM_001354896.1:c.5017_5018insACT	NP_001341825.1:p.Thr1673delinsAsnSer
NM_001354897.1:c.4993_4994insACT	NP_001341826.1:p.Thr1665delinsAsnSer
NM_001354898.1:c.4888_4889insACT	NP_001341827.1:p.Thr1630delinsAsnSer
NM_001354899.1:c.4879_4880insACT	NP_001341828.1:p.Thr1627delinsAsnSer
NM_001354900.1:c.4840_4841insACT	NP_001341829.1:p.Thr1614delinsAsnSer
NM_001354901.1:c.4786_4787insACT	NP_001341830.1:p.Thr1596delinsAsnSer
NM_001354902.1:c.4690_4691insACT	NP_001341831.1:p.Thr1564delinsAsnSer
NM_001354903.1:c.4660_4661insACT	NP_001341832.1:p.Thr1554delinsAsnSer
NM_001354904.1:c.4585_4586insACT	NP_001341833.1:p.Thr1529delinsAsnSer
NM_001354905.1:c.4483_4484insACT	NP_001341834.1:p.Thr1495delinsAsnSer
NM_001354906.1:c.4114_4115insACT	NP_001341835.1:p.Thr1372delinsAsnSer
NM_000038.6:c.4963_4964insACT MANE Select	NP_000029.2:p.Thr1655delinsAsnSer
NM_001127510.3:c.4963_4964insACT	NP_001120982.1:p.Thr1655delinsAsnSer
NM_001127511.3:c.4909_4910insACT	NP_001120983.2:p.Thr1637delinsAsnSer
NM_001354895.2:c.4963_4964insACT	NP_001341824.1:p.Thr1655delinsAsnSer
NM_001354896.2:c.5017_5018insACT	NP_001341825.1:p.Thr1673delinsAsnSer
NM_001354897.2:c.4993_4994insACT	NP_001341826.1:p.Thr1665delinsAsnSer
NM_001354898.2:c.4888_4889insACT	NP_001341827.1:p.Thr1630delinsAsnSer
NM_001354899.2:c.4879_4880insACT	NP_001341828.1:p.Thr1627delinsAsnSer
NM_001354900.2:c.4840_4841insACT	NP_001341829.1:p.Thr1614delinsAsnSer
NM_001354901.2:c.4786_4787insACT	NP_001341830.1:p.Thr1596delinsAsnSer
NM_001354902.2:c.4690_4691insACT	NP_001341831.1:p.Thr1564delinsAsnSer
NM_001354903.2:c.4660_4661insACT	NP_001341832.1:p.Thr1554delinsAsnSer
NM_001354904.2:c.4585_4586insACT	NP_001341833.1:p.Thr1529delinsAsnSer
NM_001354905.2:c.4483_4484insACT	NP_001341834.1:p.Thr1495delinsAsnSer
NM_001354906.2:c.4114_4115insACT	NP_001341835.1:p.Thr1372delinsAsnSer