Canonical Allele Identifier: CA013614
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 793
dbSNP Id: rs387906228

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112801279_112801280del , CM000667.2:g.112801279_112801280del GRCh38
NC_000005.9:g.112136976_112136977del , CM000667.1:g.112136976_112136977del GRCh37
NC_000005.8:g.112164875_112164876del NCBI36
NG_008481.4:g.113759_113760del , LRG_130:g.113759_113760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.730_731del
ENST00000504915.3:c.730_731del
ENST00000505084.2:n.786_787del
ENST00000505350.2:c.*736_*737del
ENST00000507379.6:c.676_677del
ENST00000509732.6:c.730_731del
ENST00000512211.7:c.730_731del
ENST00000257430.9:c.730_731del
ENST00000257430.8:c.730_731del
ENST00000507379.5:c.676_677del
ENST00000508376.6:c.730_731del
ENST00000508624.5:c.730_731del
ENST00000512211.6:c.730_731del
NM_000038.5:c.730_731del
NM_001127510.2:c.730_731del
NM_001127511.2:c.676_677del
NM_001354895.1:c.730_731del
NM_001354896.1:c.730_731del
NM_001354897.1:c.760_761del
NM_001354898.1:c.655_656del
NM_001354899.1:c.646_647del
NM_001354900.1:c.553_554del
NM_001354901.1:c.553_554del
NM_001354902.1:c.760_761del
NM_001354903.1:c.730_731del
NM_001354904.1:c.655_656del
NM_001354905.1:c.553_554del
NM_001354906.1:c.-306_-305del
NM_000038.6:c.730_731del
NM_001127510.3:c.730_731del
NM_001127511.3:c.676_677del
NM_001354895.2:c.730_731del
NM_001354896.2:c.730_731del
NM_001354897.2:c.760_761del
NM_001354898.2:c.655_656del
NM_001354899.2:c.646_647del
NM_001354900.2:c.553_554del
NM_001354901.2:c.553_554del
NM_001354902.2:c.760_761del
NM_001354903.2:c.730_731del
NM_001354904.2:c.655_656del
NM_001354905.2:c.553_554del
NM_001354906.2:c.-306_-305del