Canonical Allele Identifier: CA658760491
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112815594del , CM000667.2:g.112815594del GRCh38
NC_000005.9:g.112151291del , CM000667.1:g.112151291del GRCh37
NC_000005.8:g.112179190del NCBI36
NG_008481.4:g.128074del , LRG_130:g.128074del

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.933+1del
ENST00000504915.3:c.933+1del
ENST00000505084.2:n.989+1del
ENST00000505350.2:c.*939+1del
ENST00000507379.6:c.879+1del
ENST00000509732.6:c.933+1del
ENST00000512211.7:c.933+1del
ENST00000257430.9:c.933+1del
ENST00000257430.8:c.933+1del
ENST00000507379.5:c.879+1del
ENST00000508376.6:c.933+1del
ENST00000508624.5:c.*255+1del
ENST00000512211.6:c.933+1del
NM_000038.5:c.933+1del
NM_001127510.2:c.933+1del
NM_001127511.2:c.879+1del
NM_001354895.1:c.933+1del
NM_001354896.1:c.933+1del
NM_001354897.1:c.963+1del
NM_001354898.1:c.858+1del
NM_001354899.1:c.849+1del
NM_001354900.1:c.756+1del
NM_001354901.1:c.756+1del
NM_001354902.1:c.963+1del
NM_001354903.1:c.933+1del
NM_001354904.1:c.858+1del
NM_001354905.1:c.756+1del
NM_001354906.1:c.84+1del
NM_000038.6:c.933+1del
NM_001127510.3:c.933+1del
NM_001127511.3:c.879+1del
NM_001354895.2:c.933+1del
NM_001354896.2:c.933+1del
NM_001354897.2:c.963+1del
NM_001354898.2:c.858+1del
NM_001354899.2:c.849+1del
NM_001354900.2:c.756+1del
NM_001354901.2:c.756+1del
NM_001354902.2:c.963+1del
NM_001354903.2:c.933+1del
NM_001354904.2:c.858+1del
NM_001354905.2:c.756+1del
NM_001354906.2:c.84+1del