Canonical Allele Identifier: CA2710001226

Gene: APC

Linked Data

• dbSNP Id: rs2149889821

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838932del , CM000667.2:g.112838932del	GRCh38
NC_000005.9:g.112174629del , CM000667.1:g.112174629del	GRCh37
NC_000005.8:g.112202528del	NCBI36
NG_008481.4:g.151412del , LRG_130:g.151412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3003del	ENSP00000484935.2:n.3003del
ENST00000504915.3:c.3392del	ENSP00000473355.2:p.Asn1131IlefsTer13
ENST00000505350.2:c.*3344del	ENSP00000481752.1:n.*3344del
ENST00000507379.6:c.3284del	ENSP00000423224.2:p.Asn1095IlefsTer13
ENST00000509732.6:c.3338del	ENSP00000426541.2:p.Asn1113IlefsTer13
ENST00000512211.7:c.3338del	ENSP00000423828.3:p.Asn1113IlefsTer13
ENST00000257430.9:c.3338del MANE Select	ENSP00000257430.4:p.Asn1113IlefsTer13
ENST00000257430.8:c.3338del	ENSP00000257430.4:p.Asn1113IlefsTer13
ENST00000502371.2:c.1691del
ENST00000507379.5:c.3284del	ENSP00000423224.1:p.Asn1095IlefsTer13
ENST00000508376.6:c.3338del	ENSP00000427089.2:p.Asn1113IlefsTer13
ENST00000508624.5:c.*2660del	ENSP00000424265.1:n.*2660del
ENST00000512211.6:c.3338del	ENSP00000423828.2:p.Asn1113IlefsTer13
ENST00000520401.1:c.230+9960del
NM_000038.5:c.3338del	NP_000029.2:p.Asn1113IlefsTer13
NM_001127510.2:c.3338del	NP_001120982.1:p.Asn1113IlefsTer13
NM_001127511.2:c.3284del	NP_001120983.2:p.Asn1095IlefsTer13
NM_001354895.1:c.3338del	NP_001341824.1:p.Asn1113IlefsTer13
NM_001354896.1:c.3392del	NP_001341825.1:p.Asn1131IlefsTer13
NM_001354897.1:c.3368del	NP_001341826.1:p.Asn1123IlefsTer13
NM_001354898.1:c.3263del	NP_001341827.1:p.Asn1088IlefsTer13
NM_001354899.1:c.3254del	NP_001341828.1:p.Asn1085IlefsTer13
NM_001354900.1:c.3215del	NP_001341829.1:p.Asn1072IlefsTer13
NM_001354901.1:c.3161del	NP_001341830.1:p.Asn1054IlefsTer13
NM_001354902.1:c.3065del	NP_001341831.1:p.Asn1022IlefsTer13
NM_001354903.1:c.3035del	NP_001341832.1:p.Asn1012IlefsTer13
NM_001354904.1:c.2960del	NP_001341833.1:p.Asn987IlefsTer13
NM_001354905.1:c.2858del	NP_001341834.1:p.Asn953IlefsTer13
NM_001354906.1:c.2489del	NP_001341835.1:p.Asn830IlefsTer13
NM_000038.6:c.3338del MANE Select	NP_000029.2:p.Asn1113IlefsTer13
NM_001127510.3:c.3338del	NP_001120982.1:p.Asn1113IlefsTer13
NM_001127511.3:c.3284del	NP_001120983.2:p.Asn1095IlefsTer13
NM_001354895.2:c.3338del	NP_001341824.1:p.Asn1113IlefsTer13
NM_001354896.2:c.3392del	NP_001341825.1:p.Asn1131IlefsTer13
NM_001354897.2:c.3368del	NP_001341826.1:p.Asn1123IlefsTer13
NM_001354898.2:c.3263del	NP_001341827.1:p.Asn1088IlefsTer13
NM_001354899.2:c.3254del	NP_001341828.1:p.Asn1085IlefsTer13
NM_001354900.2:c.3215del	NP_001341829.1:p.Asn1072IlefsTer13
NM_001354901.2:c.3161del	NP_001341830.1:p.Asn1054IlefsTer13
NM_001354902.2:c.3065del	NP_001341831.1:p.Asn1022IlefsTer13
NM_001354903.2:c.3035del	NP_001341832.1:p.Asn1012IlefsTer13
NM_001354904.2:c.2960del	NP_001341833.1:p.Asn987IlefsTer13
NM_001354905.2:c.2858del	NP_001341834.1:p.Asn953IlefsTer13
NM_001354906.2:c.2489del	NP_001341835.1:p.Asn830IlefsTer13