Canonical Allele Identifier: CA3260675477

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815480_112815605dup , CM000667.2:g.112815480_112815605dup	GRCh38
NC_000005.9:g.112151177_112151302dup , CM000667.1:g.112151177_112151302dup	GRCh37
NC_000005.8:g.112179076_112179201dup	NCBI36
NG_008481.4:g.127960_128085dup , LRG_130:g.127960_128085dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.5:c.835-15_933+12dup
NM_000038.6:c.835-15_933+12dup
NM_001127510.2:c.835-15_933+12dup
NM_001127510.3:c.835-15_933+12dup
NM_001127511.2:c.781-15_879+12dup
NM_001127511.3:c.781-15_879+12dup
NM_001354895.1:c.835-15_933+12dup
NM_001354895.2:c.835-15_933+12dup
NM_001354896.1:c.835-15_933+12dup
NM_001354896.2:c.835-15_933+12dup
NM_001354897.1:c.865-15_963+12dup
NM_001354897.2:c.865-15_963+12dup
NM_001354898.1:c.760-15_858+12dup
NM_001354898.2:c.760-15_858+12dup
NM_001354899.1:c.751-15_849+12dup
NM_001354899.2:c.751-15_849+12dup
NM_001354900.1:c.658-15_756+12dup
NM_001354900.2:c.658-15_756+12dup
NM_001354901.1:c.658-15_756+12dup
NM_001354901.2:c.658-15_756+12dup
NM_001354902.1:c.865-15_963+12dup
NM_001354902.2:c.865-15_963+12dup
NM_001354903.1:c.835-15_933+12dup
NM_001354903.2:c.835-15_933+12dup
NM_001354904.1:c.760-15_858+12dup
NM_001354904.2:c.760-15_858+12dup
NM_001354905.1:c.658-15_756+12dup
NM_001354905.2:c.658-15_756+12dup
NM_001354906.1:c.-15-15_84+12dup
NM_001354906.2:c.-15-15_84+12dup
ENST00000257430.8:c.835-15_933+12dup
ENST00000257430.9:c.835-15_933+12dup
ENST00000502371.3:c.835-15_933+12dup
ENST00000504915.3:c.835-15_933+12dup
ENST00000505084.2:n.891-15_989+12dup
ENST00000505350.2:c.*841-15_*939+12dup
ENST00000507379.5:c.781-15_879+12dup
ENST00000507379.6:c.781-15_879+12dup
ENST00000508376.6:c.835-15_933+12dup
ENST00000508624.5:c.*157-15_*255+12dup
ENST00000509732.6:c.835-15_933+12dup
ENST00000512211.6:c.835-15_933+12dup
ENST00000512211.7:c.835-15_933+12dup