Canonical Allele Identifier: CA658683400

Gene: APC

Linked Data

• ClinVar Variation Id: 495358
• ClinVar RCV Id: RCV000588314
• dbSNP Id: rs1554084650

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838629_112838631delinsT , CM000667.2:g.112838629_112838631delinsT	GRCh38
NC_000005.9:g.112174326_112174328delinsT , CM000667.1:g.112174326_112174328delinsT	GRCh37
NC_000005.8:g.112202225_112202227delinsT	NCBI36
NG_008481.4:g.151109_151111delinsT , LRG_130:g.151109_151111delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2700_2702delinsT	ENSP00000484935.2:n.2700_2702delinsT
ENST00000504915.3:c.3089_3091delinsT	ENSP00000473355.2:p.Asn1030IlefsTer4
ENST00000505350.2:c.*3041_*3043delinsT	ENSP00000481752.1:n.*3041_*3043delinsT
ENST00000507379.6:c.2981_2983delinsT	ENSP00000423224.2:p.Asn994IlefsTer4
ENST00000509732.6:c.3035_3037delinsT	ENSP00000426541.2:p.Asn1012IlefsTer4
ENST00000512211.7:c.3035_3037delinsT	ENSP00000423828.3:p.Asn1012IlefsTer4
ENST00000257430.9:c.3035_3037delinsT MANE Select	ENSP00000257430.4:p.Asn1012IlefsTer4
ENST00000257430.8:c.3035_3037delinsT	ENSP00000257430.4:p.Asn1012IlefsTer4
ENST00000502371.2:c.1388_1390delinsT
ENST00000507379.5:c.2981_2983delinsT	ENSP00000423224.1:p.Asn994IlefsTer4
ENST00000508376.6:c.3035_3037delinsT	ENSP00000427089.2:p.Asn1012IlefsTer4
ENST00000508624.5:c.*2357_*2359delinsT	ENSP00000424265.1:n.*2357_*2359delinsT
ENST00000512211.6:c.3035_3037delinsT	ENSP00000423828.2:p.Asn1012IlefsTer4
ENST00000520401.1:c.230+9657_230+9659delinsT
NM_000038.5:c.3035_3037delinsT	NP_000029.2:p.Asn1012IlefsTer4
NM_001127510.2:c.3035_3037delinsT	NP_001120982.1:p.Asn1012IlefsTer4
NM_001127511.2:c.2981_2983delinsT	NP_001120983.2:p.Asn994IlefsTer4
NM_001354895.1:c.3035_3037delinsT	NP_001341824.1:p.Asn1012IlefsTer4
NM_001354896.1:c.3089_3091delinsT	NP_001341825.1:p.Asn1030IlefsTer4
NM_001354897.1:c.3065_3067delinsT	NP_001341826.1:p.Asn1022IlefsTer4
NM_001354898.1:c.2960_2962delinsT	NP_001341827.1:p.Asn987IlefsTer4
NM_001354899.1:c.2951_2953delinsT	NP_001341828.1:p.Asn984IlefsTer4
NM_001354900.1:c.2912_2914delinsT	NP_001341829.1:p.Asn971IlefsTer4
NM_001354901.1:c.2858_2860delinsT	NP_001341830.1:p.Asn953IlefsTer4
NM_001354902.1:c.2762_2764delinsT	NP_001341831.1:p.Asn921IlefsTer4
NM_001354903.1:c.2732_2734delinsT	NP_001341832.1:p.Asn911IlefsTer4
NM_001354904.1:c.2657_2659delinsT	NP_001341833.1:p.Asn886IlefsTer4
NM_001354905.1:c.2555_2557delinsT	NP_001341834.1:p.Asn852IlefsTer4
NM_001354906.1:c.2186_2188delinsT	NP_001341835.1:p.Asn729IlefsTer4
NM_000038.6:c.3035_3037delinsT MANE Select	NP_000029.2:p.Asn1012IlefsTer4
NM_001127510.3:c.3035_3037delinsT	NP_001120982.1:p.Asn1012IlefsTer4
NM_001127511.3:c.2981_2983delinsT	NP_001120983.2:p.Asn994IlefsTer4
NM_001354895.2:c.3035_3037delinsT	NP_001341824.1:p.Asn1012IlefsTer4
NM_001354896.2:c.3089_3091delinsT	NP_001341825.1:p.Asn1030IlefsTer4
NM_001354897.2:c.3065_3067delinsT	NP_001341826.1:p.Asn1022IlefsTer4
NM_001354898.2:c.2960_2962delinsT	NP_001341827.1:p.Asn987IlefsTer4
NM_001354899.2:c.2951_2953delinsT	NP_001341828.1:p.Asn984IlefsTer4
NM_001354900.2:c.2912_2914delinsT	NP_001341829.1:p.Asn971IlefsTer4
NM_001354901.2:c.2858_2860delinsT	NP_001341830.1:p.Asn953IlefsTer4
NM_001354902.2:c.2762_2764delinsT	NP_001341831.1:p.Asn921IlefsTer4
NM_001354903.2:c.2732_2734delinsT	NP_001341832.1:p.Asn911IlefsTer4
NM_001354904.2:c.2657_2659delinsT	NP_001341833.1:p.Asn886IlefsTer4
NM_001354905.2:c.2555_2557delinsT	NP_001341834.1:p.Asn852IlefsTer4
NM_001354906.2:c.2186_2188delinsT	NP_001341835.1:p.Asn729IlefsTer4