Canonical Allele Identifier: CA658760543

Gene: APC

Linked Data

• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839330del , CM000667.2:g.112839330del	GRCh38
NC_000005.9:g.112175027del , CM000667.1:g.112175027del	GRCh37
NC_000005.8:g.112202926del	NCBI36
NG_008481.4:g.151810del , LRG_130:g.151810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3401del	ENSP00000484935.2:n.3401del
ENST00000504915.3:c.3790del	ENSP00000473355.2:p.Ala1264LeufsTer19
ENST00000505350.2:c.*3742del	ENSP00000481752.1:n.*3742del
ENST00000507379.6:c.3682del	ENSP00000423224.2:p.Ala1228LeufsTer19
ENST00000509732.6:c.3736del	ENSP00000426541.2:p.Ala1246LeufsTer19
ENST00000512211.7:c.3736del	ENSP00000423828.3:p.Ala1246LeufsTer19
ENST00000257430.9:c.3736del MANE Select	ENSP00000257430.4:p.Ala1246LeufsTer19
ENST00000257430.8:c.3736del	ENSP00000257430.4:p.Ala1246LeufsTer19
ENST00000502371.2:c.2089del
ENST00000508376.6:c.3736del	ENSP00000427089.2:p.Ala1246LeufsTer19
ENST00000508624.5:c.*3058del	ENSP00000424265.1:n.*3058del
ENST00000512211.6:c.3736del	ENSP00000423828.2:p.Ala1246LeufsTer19
ENST00000520401.1:c.230+10358del
NM_000038.5:c.3736del	NP_000029.2:p.Ala1246LeufsTer19
NM_001127510.2:c.3736del	NP_001120982.1:p.Ala1246LeufsTer19
NM_001127511.2:c.3682del	NP_001120983.2:p.Ala1228LeufsTer19
NM_001354895.1:c.3736del	NP_001341824.1:p.Ala1246LeufsTer19
NM_001354896.1:c.3790del	NP_001341825.1:p.Ala1264LeufsTer19
NM_001354897.1:c.3766del	NP_001341826.1:p.Ala1256LeufsTer19
NM_001354898.1:c.3661del	NP_001341827.1:p.Ala1221LeufsTer19
NM_001354899.1:c.3652del	NP_001341828.1:p.Ala1218LeufsTer19
NM_001354900.1:c.3613del	NP_001341829.1:p.Ala1205LeufsTer19
NM_001354901.1:c.3559del	NP_001341830.1:p.Ala1187LeufsTer19
NM_001354902.1:c.3463del	NP_001341831.1:p.Ala1155LeufsTer19
NM_001354903.1:c.3433del	NP_001341832.1:p.Ala1145LeufsTer19
NM_001354904.1:c.3358del	NP_001341833.1:p.Ala1120LeufsTer19
NM_001354905.1:c.3256del	NP_001341834.1:p.Ala1086LeufsTer19
NM_001354906.1:c.2887del	NP_001341835.1:p.Ala963LeufsTer19
NM_000038.6:c.3736del MANE Select	NP_000029.2:p.Ala1246LeufsTer19
NM_001127510.3:c.3736del	NP_001120982.1:p.Ala1246LeufsTer19
NM_001127511.3:c.3682del	NP_001120983.2:p.Ala1228LeufsTer19
NM_001354895.2:c.3736del	NP_001341824.1:p.Ala1246LeufsTer19
NM_001354896.2:c.3790del	NP_001341825.1:p.Ala1264LeufsTer19
NM_001354897.2:c.3766del	NP_001341826.1:p.Ala1256LeufsTer19
NM_001354898.2:c.3661del	NP_001341827.1:p.Ala1221LeufsTer19
NM_001354899.2:c.3652del	NP_001341828.1:p.Ala1218LeufsTer19
NM_001354900.2:c.3613del	NP_001341829.1:p.Ala1205LeufsTer19
NM_001354901.2:c.3559del	NP_001341830.1:p.Ala1187LeufsTer19
NM_001354902.2:c.3463del	NP_001341831.1:p.Ala1155LeufsTer19
NM_001354903.2:c.3433del	NP_001341832.1:p.Ala1145LeufsTer19
NM_001354904.2:c.3358del	NP_001341833.1:p.Ala1120LeufsTer19
NM_001354905.2:c.3256del	NP_001341834.1:p.Ala1086LeufsTer19
NM_001354906.2:c.2887del	NP_001341835.1:p.Ala963LeufsTer19