Canonical Allele Identifier: CA1573474945

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843538_112843548delinsACCTGCTGTTT , CM000667.2:g.112843538_112843548delinsACCTGCTGTTT	GRCh38
NC_000005.9:g.112179235_112179245delinsACCTGCTGTTT , CM000667.1:g.112179235_112179245delinsACCTGCTGTTT	GRCh37
NC_000005.8:g.112207134_112207144delinsACCTGCTGTTT	NCBI36
NG_008481.4:g.156018_156028delinsACCTGCTGTTT , LRG_130:g.156018_156028delinsACCTGCTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7998_8008delinsACCTGCTGTTT	ENSP00000473355.2:p.Ala2666=
ENST00000505350.2:c.*7950_*7960delinsACCTGCTGTTT	ENSP00000481752.1:n.*7950_*7960delinsACCTGCTGTTT
ENST00000507379.6:c.7890_7900delinsACCTGCTGTTT	ENSP00000423224.2:p.Ala2630=
ENST00000509732.6:c.7944_7954delinsACCTGCTGTTT	ENSP00000426541.2:p.Ala2648=
ENST00000512211.7:c.7944_7954delinsACCTGCTGTTT	ENSP00000423828.3:p.Ala2648=
ENST00000257430.9:c.7944_7954delinsACCTGCTGTTT MANE Select	ENSP00000257430.4:p.Ala2648=
ENST00000257430.8:c.7944_7954delinsACCTGCTGTTT	ENSP00000257430.4:p.Ala2648=
ENST00000508376.6:c.7944_7954delinsACCTGCTGTTT	ENSP00000427089.2:p.Ala2648=
ENST00000520401.1:c.231-13111_231-13101delinsACCTGCTGTTT
NM_000038.5:c.7944_7954delinsACCTGCTGTTT	NP_000029.2:p.Ala2648=
NM_001127510.2:c.7944_7954delinsACCTGCTGTTT	NP_001120982.1:p.Ala2648=
NM_001127511.2:c.7890_7900delinsACCTGCTGTTT	NP_001120983.2:p.Ala2630=
NM_001354895.1:c.7944_7954delinsACCTGCTGTTT	NP_001341824.1:p.Ala2648=
NM_001354896.1:c.7998_8008delinsACCTGCTGTTT	NP_001341825.1:p.Ala2666=
NM_001354897.1:c.7974_7984delinsACCTGCTGTTT	NP_001341826.1:p.Ala2658=
NM_001354898.1:c.7869_7879delinsACCTGCTGTTT	NP_001341827.1:p.Ala2623=
NM_001354899.1:c.7860_7870delinsACCTGCTGTTT	NP_001341828.1:p.Ala2620=
NM_001354900.1:c.7821_7831delinsACCTGCTGTTT	NP_001341829.1:p.Ala2607=
NM_001354901.1:c.7767_7777delinsACCTGCTGTTT	NP_001341830.1:p.Ala2589=
NM_001354902.1:c.7671_7681delinsACCTGCTGTTT	NP_001341831.1:p.Ala2557=
NM_001354903.1:c.7641_7651delinsACCTGCTGTTT	NP_001341832.1:p.Ala2547=
NM_001354904.1:c.7566_7576delinsACCTGCTGTTT	NP_001341833.1:p.Ala2522=
NM_001354905.1:c.7464_7474delinsACCTGCTGTTT	NP_001341834.1:p.Ala2488=
NM_001354906.1:c.7095_7105delinsACCTGCTGTTT	NP_001341835.1:p.Ala2365=
NM_000038.6:c.7944_7954delinsACCTGCTGTTT MANE Select	NP_000029.2:p.Ala2648=
NM_001127510.3:c.7944_7954delinsACCTGCTGTTT	NP_001120982.1:p.Ala2648=
NM_001127511.3:c.7890_7900delinsACCTGCTGTTT	NP_001120983.2:p.Ala2630=
NM_001354895.2:c.7944_7954delinsACCTGCTGTTT	NP_001341824.1:p.Ala2648=
NM_001354896.2:c.7998_8008delinsACCTGCTGTTT	NP_001341825.1:p.Ala2666=
NM_001354897.2:c.7974_7984delinsACCTGCTGTTT	NP_001341826.1:p.Ala2658=
NM_001354898.2:c.7869_7879delinsACCTGCTGTTT	NP_001341827.1:p.Ala2623=
NM_001354899.2:c.7860_7870delinsACCTGCTGTTT	NP_001341828.1:p.Ala2620=
NM_001354900.2:c.7821_7831delinsACCTGCTGTTT	NP_001341829.1:p.Ala2607=
NM_001354901.2:c.7767_7777delinsACCTGCTGTTT	NP_001341830.1:p.Ala2589=
NM_001354902.2:c.7671_7681delinsACCTGCTGTTT	NP_001341831.1:p.Ala2557=
NM_001354903.2:c.7641_7651delinsACCTGCTGTTT	NP_001341832.1:p.Ala2547=
NM_001354904.2:c.7566_7576delinsACCTGCTGTTT	NP_001341833.1:p.Ala2522=
NM_001354905.2:c.7464_7474delinsACCTGCTGTTT	NP_001341834.1:p.Ala2488=
NM_001354906.2:c.7095_7105delinsACCTGCTGTTT	NP_001341835.1:p.Ala2365=