Canonical Allele Identifier: CA658760556
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112819294_112819295delinsAA , CM000667.2:g.112819294_112819295delinsAA GRCh38
NC_000005.9:g.112154991_112154992delinsAA , CM000667.1:g.112154991_112154992delinsAA GRCh37
NC_000005.8:g.112182890_112182891delinsAA NCBI36
NG_008481.4:g.131774_131775delinsAA , LRG_130:g.131774_131775delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.1262_1263delinsAA ENSP00000484935.2:p.Trp421Ter
ENST00000504915.3:c.1262_1263delinsAA ENSP00000473355.2:p.Trp421Ter
ENST00000505084.2:n.1318_1319delinsAA
ENST00000505350.2:c.*1268_*1269delinsAA ENSP00000481752.1:n.*1268_*1269delinsAA
ENST00000507379.6:c.1208_1209delinsAA ENSP00000423224.2:p.Trp403Ter
ENST00000509732.6:c.1262_1263delinsAA ENSP00000426541.2:p.Trp421Ter
ENST00000512211.7:c.1262_1263delinsAA ENSP00000423828.3:p.Trp421Ter
ENST00000257430.9:c.1262_1263delinsAA MANE Select ENSP00000257430.4:p.Trp421Ter
ENST00000257430.8:c.1262_1263delinsAA ENSP00000257430.4:p.Trp421Ter
ENST00000507379.5:c.1208_1209delinsAA ENSP00000423224.1:p.Trp403Ter
ENST00000508376.6:c.1262_1263delinsAA ENSP00000427089.2:p.Trp421Ter
ENST00000508624.5:c.*584_*585delinsAA ENSP00000424265.1:n.*584_*585delinsAA
ENST00000512211.6:c.1262_1263delinsAA ENSP00000423828.2:p.Trp421Ter
NM_000038.5:c.1262_1263delinsAA NP_000029.2:p.Trp421Ter
NM_001127510.2:c.1262_1263delinsAA NP_001120982.1:p.Trp421Ter
NM_001127511.2:c.1208_1209delinsAA NP_001120983.2:p.Trp403Ter
NM_001354895.1:c.1262_1263delinsAA NP_001341824.1:p.Trp421Ter
NM_001354896.1:c.1262_1263delinsAA NP_001341825.1:p.Trp421Ter
NM_001354897.1:c.1292_1293delinsAA NP_001341826.1:p.Trp431Ter
NM_001354898.1:c.1187_1188delinsAA NP_001341827.1:p.Trp396Ter
NM_001354899.1:c.1178_1179delinsAA NP_001341828.1:p.Trp393Ter
NM_001354900.1:c.1085_1086delinsAA NP_001341829.1:p.Trp362Ter
NM_001354901.1:c.1085_1086delinsAA NP_001341830.1:p.Trp362Ter
NM_001354902.1:c.989_990delinsAA NP_001341831.1:p.Trp330Ter
NM_001354903.1:c.959_960delinsAA NP_001341832.1:p.Trp320Ter
NM_001354904.1:c.884_885delinsAA NP_001341833.1:p.Trp295Ter
NM_001354905.1:c.782_783delinsAA NP_001341834.1:p.Trp261Ter
NM_001354906.1:c.413_414delinsAA NP_001341835.1:p.Trp138Ter
NM_000038.6:c.1262_1263delinsAA MANE Select NP_000029.2:p.Trp421Ter
NM_001127510.3:c.1262_1263delinsAA NP_001120982.1:p.Trp421Ter
NM_001127511.3:c.1208_1209delinsAA NP_001120983.2:p.Trp403Ter
NM_001354895.2:c.1262_1263delinsAA NP_001341824.1:p.Trp421Ter
NM_001354896.2:c.1262_1263delinsAA NP_001341825.1:p.Trp421Ter
NM_001354897.2:c.1292_1293delinsAA NP_001341826.1:p.Trp431Ter
NM_001354898.2:c.1187_1188delinsAA NP_001341827.1:p.Trp396Ter
NM_001354899.2:c.1178_1179delinsAA NP_001341828.1:p.Trp393Ter
NM_001354900.2:c.1085_1086delinsAA NP_001341829.1:p.Trp362Ter
NM_001354901.2:c.1085_1086delinsAA NP_001341830.1:p.Trp362Ter
NM_001354902.2:c.989_990delinsAA NP_001341831.1:p.Trp330Ter
NM_001354903.2:c.959_960delinsAA NP_001341832.1:p.Trp320Ter
NM_001354904.2:c.884_885delinsAA NP_001341833.1:p.Trp295Ter
NM_001354905.2:c.782_783delinsAA NP_001341834.1:p.Trp261Ter
NM_001354906.2:c.413_414delinsAA NP_001341835.1:p.Trp138Ter