Canonical Allele Identifier: CA1573492010
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112788676_112788677delinsAG , CM000667.2:g.112788676_112788677delinsAG GRCh38
NC_000005.9:g.112124373_112124374delinsAG , CM000667.1:g.112124373_112124374delinsAG GRCh37
NC_000005.8:g.112152272_112152273delinsAG NCBI36
NG_008481.4:g.101156_101157delinsAG , LRG_130:g.101156_101157delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.646-3770_646-3769delinsAG MANE Select ENSP00000257430.4:n.646-3770_646-3769deli...
ENST00000257430.8:c.646-3770_646-3769delinsAG ENSP00000257430.4:n.646-3770_646-3769deli...
ENST00000507379.5:c.675+7773_675+7774delinsAG ENSP00000423224.1:n.675+7773_675+7774deli...
ENST00000508376.6:c.646-3770_646-3769delinsAG ENSP00000427089.2:n.646-3770_646-3769deli...
ENST00000508624.5:c.646-3770_646-3769delinsAG ENSP00000424265.1:n.646-3770_646-3769deli...
ENST00000512211.6:c.646-3770_646-3769delinsAG ENSP00000423828.2:n.646-3770_646-3769deli...
NM_000038.5:c.646-3770_646-3769delinsAG NP_000029.2:n.646-3770_646-3769delinsAG
NM_001127510.2:c.646-3770_646-3769delinsAG NP_001120982.1:n.646-3770_646-3769delinsA...
NM_001127511.2:c.675+7773_675+7774delinsAG NP_001120983.2:n.675+7773_675+7774delinsA...
NM_001354895.1:c.646-3770_646-3769delinsAG NP_001341824.1:n.646-3770_646-3769delinsA...
NM_001354896.1:c.646-3770_646-3769delinsAG NP_001341825.1:n.646-3770_646-3769delinsA...
NM_001354897.1:c.676-3770_676-3769delinsAG NP_001341826.1:n.676-3770_676-3769delinsA...
NM_001354898.1:c.571-3770_571-3769delinsAG NP_001341827.1:n.571-3770_571-3769delinsA...
NM_001354899.1:c.645+7773_645+7774delinsAG NP_001341828.1:n.645+7773_645+7774delinsA...
NM_001354900.1:c.469-3770_469-3769delinsAG NP_001341829.1:n.469-3770_469-3769delinsA...
NM_001354901.1:c.469-3770_469-3769delinsAG NP_001341830.1:n.469-3770_469-3769delinsA...
NM_001354902.1:c.676-3770_676-3769delinsAG NP_001341831.1:n.676-3770_676-3769delinsA...
NM_001354903.1:c.646-3770_646-3769delinsAG NP_001341832.1:n.646-3770_646-3769delinsA...
NM_001354904.1:c.571-3770_571-3769delinsAG NP_001341833.1:n.571-3770_571-3769delinsA...
NM_001354905.1:c.469-3770_469-3769delinsAG NP_001341834.1:n.469-3770_469-3769delinsA...
NM_001354906.1:c.-390-3770_-390-3769delinsAG NP_001341835.1:n.-390-3770_-390-3769delin...
NM_000038.6:c.646-3770_646-3769delinsAG MANE Select NP_000029.2:n.646-3770_646-3769delinsAG
NM_001127510.3:c.646-3770_646-3769delinsAG NP_001120982.1:n.646-3770_646-3769delinsA...
NM_001127511.3:c.675+7773_675+7774delinsAG NP_001120983.2:n.675+7773_675+7774delinsA...
NM_001354895.2:c.646-3770_646-3769delinsAG NP_001341824.1:n.646-3770_646-3769delinsA...
NM_001354896.2:c.646-3770_646-3769delinsAG NP_001341825.1:n.646-3770_646-3769delinsA...
NM_001354897.2:c.676-3770_676-3769delinsAG NP_001341826.1:n.676-3770_676-3769delinsA...
NM_001354898.2:c.571-3770_571-3769delinsAG NP_001341827.1:n.571-3770_571-3769delinsA...
NM_001354899.2:c.645+7773_645+7774delinsAG NP_001341828.1:n.645+7773_645+7774delinsA...
NM_001354900.2:c.469-3770_469-3769delinsAG NP_001341829.1:n.469-3770_469-3769delinsA...
NM_001354901.2:c.469-3770_469-3769delinsAG NP_001341830.1:n.469-3770_469-3769delinsA...
NM_001354902.2:c.676-3770_676-3769delinsAG NP_001341831.1:n.676-3770_676-3769delinsA...
NM_001354903.2:c.646-3770_646-3769delinsAG NP_001341832.1:n.646-3770_646-3769delinsA...
NM_001354904.2:c.571-3770_571-3769delinsAG NP_001341833.1:n.571-3770_571-3769delinsA...
NM_001354905.2:c.469-3770_469-3769delinsAG NP_001341834.1:n.469-3770_469-3769delinsA...
NM_001354906.2:c.-390-3770_-390-3769delinsAG NP_001341835.1:n.-390-3770_-390-3769delin...