Canonical Allele Identifier: CA1573476118

Gene: APC

Linked Data

• dbSNP Id: rs1766649275

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843712_112843713insTCG , CM000667.2:g.112843712_112843713insTCG	GRCh38
NC_000005.9:g.112179409_112179410insTCG , CM000667.1:g.112179409_112179410insTCG	GRCh37
NC_000005.8:g.112207308_112207309insTCG	NCBI36
NG_008481.4:g.156192_156193insTCG , LRG_130:g.156192_156193insTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8172_8173insTCG	ENSP00000473355.2:p.Val2724_Gly2725insSer
ENST00000505350.2:c.*8124_*8125insTCG	ENSP00000481752.1:n.*8124_*8125insTCG
ENST00000507379.6:c.8064_8065insTCG	ENSP00000423224.2:p.Val2688_Gly2689insSer
ENST00000509732.6:c.8118_8119insTCG	ENSP00000426541.2:p.Val2706_Gly2707insSer
ENST00000512211.7:c.8118_8119insTCG	ENSP00000423828.3:p.Val2706_Gly2707insSer
ENST00000257430.9:c.8118_8119insTCG MANE Select	ENSP00000257430.4:p.Val2706_Gly2707insSer
ENST00000257430.8:c.8118_8119insTCG	ENSP00000257430.4:p.Val2706_Gly2707insSer
ENST00000508376.6:c.8118_8119insTCG	ENSP00000427089.2:p.Val2706_Gly2707insSer
ENST00000520401.1:c.231-12937_231-12936insTCG
NM_000038.5:c.8118_8119insTCG	NP_000029.2:p.Val2706_Gly2707insSer
NM_001127510.2:c.8118_8119insTCG	NP_001120982.1:p.Val2706_Gly2707insSer
NM_001127511.2:c.8064_8065insTCG	NP_001120983.2:p.Val2688_Gly2689insSer
NM_001354895.1:c.8118_8119insTCG	NP_001341824.1:p.Val2706_Gly2707insSer
NM_001354896.1:c.8172_8173insTCG	NP_001341825.1:p.Val2724_Gly2725insSer
NM_001354897.1:c.8148_8149insTCG	NP_001341826.1:p.Val2716_Gly2717insSer
NM_001354898.1:c.8043_8044insTCG	NP_001341827.1:p.Val2681_Gly2682insSer
NM_001354899.1:c.8034_8035insTCG	NP_001341828.1:p.Val2678_Gly2679insSer
NM_001354900.1:c.7995_7996insTCG	NP_001341829.1:p.Val2665_Gly2666insSer
NM_001354901.1:c.7941_7942insTCG	NP_001341830.1:p.Val2647_Gly2648insSer
NM_001354902.1:c.7845_7846insTCG	NP_001341831.1:p.Val2615_Gly2616insSer
NM_001354903.1:c.7815_7816insTCG	NP_001341832.1:p.Val2605_Gly2606insSer
NM_001354904.1:c.7740_7741insTCG	NP_001341833.1:p.Val2580_Gly2581insSer
NM_001354905.1:c.7638_7639insTCG	NP_001341834.1:p.Val2546_Gly2547insSer
NM_001354906.1:c.7269_7270insTCG	NP_001341835.1:p.Val2423_Gly2424insSer
NM_000038.6:c.8118_8119insTCG MANE Select	NP_000029.2:p.Val2706_Gly2707insSer
NM_001127510.3:c.8118_8119insTCG	NP_001120982.1:p.Val2706_Gly2707insSer
NM_001127511.3:c.8064_8065insTCG	NP_001120983.2:p.Val2688_Gly2689insSer
NM_001354895.2:c.8118_8119insTCG	NP_001341824.1:p.Val2706_Gly2707insSer
NM_001354896.2:c.8172_8173insTCG	NP_001341825.1:p.Val2724_Gly2725insSer
NM_001354897.2:c.8148_8149insTCG	NP_001341826.1:p.Val2716_Gly2717insSer
NM_001354898.2:c.8043_8044insTCG	NP_001341827.1:p.Val2681_Gly2682insSer
NM_001354899.2:c.8034_8035insTCG	NP_001341828.1:p.Val2678_Gly2679insSer
NM_001354900.2:c.7995_7996insTCG	NP_001341829.1:p.Val2665_Gly2666insSer
NM_001354901.2:c.7941_7942insTCG	NP_001341830.1:p.Val2647_Gly2648insSer
NM_001354902.2:c.7845_7846insTCG	NP_001341831.1:p.Val2615_Gly2616insSer
NM_001354903.2:c.7815_7816insTCG	NP_001341832.1:p.Val2605_Gly2606insSer
NM_001354904.2:c.7740_7741insTCG	NP_001341833.1:p.Val2580_Gly2581insSer
NM_001354905.2:c.7638_7639insTCG	NP_001341834.1:p.Val2546_Gly2547insSer
NM_001354906.2:c.7269_7270insTCG	NP_001341835.1:p.Val2423_Gly2424insSer