Canonical Allele Identifier: CA2695204937

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839013del , CM000667.2:g.112839013del	GRCh38
NC_000005.9:g.112174710del , CM000667.1:g.112174710del	GRCh37
NC_000005.8:g.112202609del	NCBI36
NG_008481.4:g.151493del , LRG_130:g.151493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3084del	ENSP00000484935.2:n.3084del
ENST00000504915.3:c.3473del	ENSP00000473355.2:p.Pro1158LeufsTer25
ENST00000505350.2:c.*3425del	ENSP00000481752.1:n.*3425del
ENST00000507379.6:c.3365del	ENSP00000423224.2:p.Pro1122LeufsTer25
ENST00000509732.6:c.3419del	ENSP00000426541.2:p.Pro1140LeufsTer25
ENST00000512211.7:c.3419del	ENSP00000423828.3:p.Pro1140LeufsTer25
ENST00000257430.9:c.3419del MANE Select	ENSP00000257430.4:p.Pro1140LeufsTer25
ENST00000257430.8:c.3419del	ENSP00000257430.4:p.Pro1140LeufsTer25
ENST00000502371.2:c.1772del
ENST00000507379.5:c.3365del	ENSP00000423224.1:p.Pro1122LeufsTer?
ENST00000508376.6:c.3419del	ENSP00000427089.2:p.Pro1140LeufsTer25
ENST00000508624.5:c.*2741del	ENSP00000424265.1:n.*2741del
ENST00000512211.6:c.3419del	ENSP00000423828.2:p.Pro1140LeufsTer25
ENST00000520401.1:c.230+10041del
NM_000038.5:c.3419del	NP_000029.2:p.Pro1140LeufsTer25
NM_001127510.2:c.3419del	NP_001120982.1:p.Pro1140LeufsTer25
NM_001127511.2:c.3365del	NP_001120983.2:p.Pro1122LeufsTer25
NM_001354895.1:c.3419del	NP_001341824.1:p.Pro1140LeufsTer25
NM_001354896.1:c.3473del	NP_001341825.1:p.Pro1158LeufsTer25
NM_001354897.1:c.3449del	NP_001341826.1:p.Pro1150LeufsTer25
NM_001354898.1:c.3344del	NP_001341827.1:p.Pro1115LeufsTer25
NM_001354899.1:c.3335del	NP_001341828.1:p.Pro1112LeufsTer25
NM_001354900.1:c.3296del	NP_001341829.1:p.Pro1099LeufsTer25
NM_001354901.1:c.3242del	NP_001341830.1:p.Pro1081LeufsTer25
NM_001354902.1:c.3146del	NP_001341831.1:p.Pro1049LeufsTer25
NM_001354903.1:c.3116del	NP_001341832.1:p.Pro1039LeufsTer25
NM_001354904.1:c.3041del	NP_001341833.1:p.Pro1014LeufsTer25
NM_001354905.1:c.2939del	NP_001341834.1:p.Pro980LeufsTer25
NM_001354906.1:c.2570del	NP_001341835.1:p.Pro857LeufsTer25
NM_000038.6:c.3419del MANE Select	NP_000029.2:p.Pro1140LeufsTer25
NM_001127510.3:c.3419del	NP_001120982.1:p.Pro1140LeufsTer25
NM_001127511.3:c.3365del	NP_001120983.2:p.Pro1122LeufsTer25
NM_001354895.2:c.3419del	NP_001341824.1:p.Pro1140LeufsTer25
NM_001354896.2:c.3473del	NP_001341825.1:p.Pro1158LeufsTer25
NM_001354897.2:c.3449del	NP_001341826.1:p.Pro1150LeufsTer25
NM_001354898.2:c.3344del	NP_001341827.1:p.Pro1115LeufsTer25
NM_001354899.2:c.3335del	NP_001341828.1:p.Pro1112LeufsTer25
NM_001354900.2:c.3296del	NP_001341829.1:p.Pro1099LeufsTer25
NM_001354901.2:c.3242del	NP_001341830.1:p.Pro1081LeufsTer25
NM_001354902.2:c.3146del	NP_001341831.1:p.Pro1049LeufsTer25
NM_001354903.2:c.3116del	NP_001341832.1:p.Pro1039LeufsTer25
NM_001354904.2:c.3041del	NP_001341833.1:p.Pro1014LeufsTer25
NM_001354905.2:c.2939del	NP_001341834.1:p.Pro980LeufsTer25
NM_001354906.2:c.2570del	NP_001341835.1:p.Pro857LeufsTer25