Canonical Allele Identifier: CA2582341638

Gene: APC

Linked Data

• ClinVar Variation Id: 2583661
• ClinVar RCV Id: RCV003337495

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843560_112843562delinsTA , CM000667.2:g.112843560_112843562delinsTA	GRCh38
NC_000005.9:g.112179257_112179259delinsTA , CM000667.1:g.112179257_112179259delinsTA	GRCh37
NC_000005.8:g.112207156_112207158delinsTA	NCBI36
NG_008481.4:g.156040_156042delinsTA , LRG_130:g.156040_156042delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8020_8022delinsTA	ENSP00000473355.2:p.Asp2674Ter
ENST00000505350.2:c.*7972_*7974delinsTA	ENSP00000481752.1:n.*7972_*7974delinsTA
ENST00000507379.6:c.7912_7914delinsTA	ENSP00000423224.2:p.Asp2638Ter
ENST00000509732.6:c.7966_7968delinsTA	ENSP00000426541.2:p.Asp2656Ter
ENST00000512211.7:c.7966_7968delinsTA	ENSP00000423828.3:p.Asp2656Ter
ENST00000257430.9:c.7966_7968delinsTA MANE Select	ENSP00000257430.4:p.Asp2656Ter
ENST00000257430.8:c.7966_7968delinsTA	ENSP00000257430.4:p.Asp2656Ter
ENST00000508376.6:c.7966_7968delinsTA	ENSP00000427089.2:p.Asp2656Ter
ENST00000520401.1:c.231-13089_231-13087delinsTA
NM_000038.5:c.7966_7968delinsTA	NP_000029.2:p.Asp2656Ter
NM_001127510.2:c.7966_7968delinsTA	NP_001120982.1:p.Asp2656Ter
NM_001127511.2:c.7912_7914delinsTA	NP_001120983.2:p.Asp2638Ter
NM_001354895.1:c.7966_7968delinsTA	NP_001341824.1:p.Asp2656Ter
NM_001354896.1:c.8020_8022delinsTA	NP_001341825.1:p.Asp2674Ter
NM_001354897.1:c.7996_7998delinsTA	NP_001341826.1:p.Asp2666Ter
NM_001354898.1:c.7891_7893delinsTA	NP_001341827.1:p.Asp2631Ter
NM_001354899.1:c.7882_7884delinsTA	NP_001341828.1:p.Asp2628Ter
NM_001354900.1:c.7843_7845delinsTA	NP_001341829.1:p.Asp2615Ter
NM_001354901.1:c.7789_7791delinsTA	NP_001341830.1:p.Asp2597Ter
NM_001354902.1:c.7693_7695delinsTA	NP_001341831.1:p.Asp2565Ter
NM_001354903.1:c.7663_7665delinsTA	NP_001341832.1:p.Asp2555Ter
NM_001354904.1:c.7588_7590delinsTA	NP_001341833.1:p.Asp2530Ter
NM_001354905.1:c.7486_7488delinsTA	NP_001341834.1:p.Asp2496Ter
NM_001354906.1:c.7117_7119delinsTA	NP_001341835.1:p.Asp2373Ter
NM_000038.6:c.7966_7968delinsTA MANE Select	NP_000029.2:p.Asp2656Ter
NM_001127510.3:c.7966_7968delinsTA	NP_001120982.1:p.Asp2656Ter
NM_001127511.3:c.7912_7914delinsTA	NP_001120983.2:p.Asp2638Ter
NM_001354895.2:c.7966_7968delinsTA	NP_001341824.1:p.Asp2656Ter
NM_001354896.2:c.8020_8022delinsTA	NP_001341825.1:p.Asp2674Ter
NM_001354897.2:c.7996_7998delinsTA	NP_001341826.1:p.Asp2666Ter
NM_001354898.2:c.7891_7893delinsTA	NP_001341827.1:p.Asp2631Ter
NM_001354899.2:c.7882_7884delinsTA	NP_001341828.1:p.Asp2628Ter
NM_001354900.2:c.7843_7845delinsTA	NP_001341829.1:p.Asp2615Ter
NM_001354901.2:c.7789_7791delinsTA	NP_001341830.1:p.Asp2597Ter
NM_001354902.2:c.7693_7695delinsTA	NP_001341831.1:p.Asp2565Ter
NM_001354903.2:c.7663_7665delinsTA	NP_001341832.1:p.Asp2555Ter
NM_001354904.2:c.7588_7590delinsTA	NP_001341833.1:p.Asp2530Ter
NM_001354905.2:c.7486_7488delinsTA	NP_001341834.1:p.Asp2496Ter
NM_001354906.2:c.7117_7119delinsTA	NP_001341835.1:p.Asp2373Ter