Canonical Allele Identifier: CA2582341510

Gene: APC

Linked Data

• ClinVar Variation Id: 2583221
• ClinVar RCV Id: RCV003336892 ; RCV003475565

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838943del , CM000667.2:g.112838943del	GRCh38
NC_000005.9:g.112174640del , CM000667.1:g.112174640del	GRCh37
NC_000005.8:g.112202539del	NCBI36
NG_008481.4:g.151423del , LRG_130:g.151423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3014del	ENSP00000484935.2:n.3014del
ENST00000504915.3:c.3403del	ENSP00000473355.2:p.Ser1135LeufsTer9
ENST00000505350.2:c.*3355del	ENSP00000481752.1:n.*3355del
ENST00000507379.6:c.3295del	ENSP00000423224.2:p.Ser1099LeufsTer9
ENST00000509732.6:c.3349del	ENSP00000426541.2:p.Ser1117LeufsTer9
ENST00000512211.7:c.3349del	ENSP00000423828.3:p.Ser1117LeufsTer9
ENST00000257430.9:c.3349del MANE Select	ENSP00000257430.4:p.Ser1117LeufsTer9
ENST00000257430.8:c.3349del	ENSP00000257430.4:p.Ser1117LeufsTer9
ENST00000502371.2:c.1702del
ENST00000507379.5:c.3295del	ENSP00000423224.1:p.Ser1099LeufsTer9
ENST00000508376.6:c.3349del	ENSP00000427089.2:p.Ser1117LeufsTer9
ENST00000508624.5:c.*2671del	ENSP00000424265.1:n.*2671del
ENST00000512211.6:c.3349del	ENSP00000423828.2:p.Ser1117LeufsTer9
ENST00000520401.1:c.230+9971del
NM_000038.5:c.3349del	NP_000029.2:p.Ser1117LeufsTer9
NM_001127510.2:c.3349del	NP_001120982.1:p.Ser1117LeufsTer9
NM_001127511.2:c.3295del	NP_001120983.2:p.Ser1099LeufsTer9
NM_001354895.1:c.3349del	NP_001341824.1:p.Ser1117LeufsTer9
NM_001354896.1:c.3403del	NP_001341825.1:p.Ser1135LeufsTer9
NM_001354897.1:c.3379del	NP_001341826.1:p.Ser1127LeufsTer9
NM_001354898.1:c.3274del	NP_001341827.1:p.Ser1092LeufsTer9
NM_001354899.1:c.3265del	NP_001341828.1:p.Ser1089LeufsTer9
NM_001354900.1:c.3226del	NP_001341829.1:p.Ser1076LeufsTer9
NM_001354901.1:c.3172del	NP_001341830.1:p.Ser1058LeufsTer9
NM_001354902.1:c.3076del	NP_001341831.1:p.Ser1026LeufsTer9
NM_001354903.1:c.3046del	NP_001341832.1:p.Ser1016LeufsTer9
NM_001354904.1:c.2971del	NP_001341833.1:p.Ser991LeufsTer9
NM_001354905.1:c.2869del	NP_001341834.1:p.Ser957LeufsTer9
NM_001354906.1:c.2500del	NP_001341835.1:p.Ser834LeufsTer9
NM_000038.6:c.3349del MANE Select	NP_000029.2:p.Ser1117LeufsTer9
NM_001127510.3:c.3349del	NP_001120982.1:p.Ser1117LeufsTer9
NM_001127511.3:c.3295del	NP_001120983.2:p.Ser1099LeufsTer9
NM_001354895.2:c.3349del	NP_001341824.1:p.Ser1117LeufsTer9
NM_001354896.2:c.3403del	NP_001341825.1:p.Ser1135LeufsTer9
NM_001354897.2:c.3379del	NP_001341826.1:p.Ser1127LeufsTer9
NM_001354898.2:c.3274del	NP_001341827.1:p.Ser1092LeufsTer9
NM_001354899.2:c.3265del	NP_001341828.1:p.Ser1089LeufsTer9
NM_001354900.2:c.3226del	NP_001341829.1:p.Ser1076LeufsTer9
NM_001354901.2:c.3172del	NP_001341830.1:p.Ser1058LeufsTer9
NM_001354902.2:c.3076del	NP_001341831.1:p.Ser1026LeufsTer9
NM_001354903.2:c.3046del	NP_001341832.1:p.Ser1016LeufsTer9
NM_001354904.2:c.2971del	NP_001341833.1:p.Ser991LeufsTer9
NM_001354905.2:c.2869del	NP_001341834.1:p.Ser957LeufsTer9
NM_001354906.2:c.2500del	NP_001341835.1:p.Ser834LeufsTer9