Canonical Allele Identifier: CA1573479869

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841566_112841567delinsAG , CM000667.2:g.112841566_112841567delinsAG	GRCh38
NC_000005.9:g.112177263_112177264delinsAG , CM000667.1:g.112177263_112177264delinsAG	GRCh37
NC_000005.8:g.112205162_112205163delinsAG	NCBI36
NG_008481.4:g.154046_154047delinsAG , LRG_130:g.154046_154047delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.6026_6027delinsAG	ENSP00000473355.2:p.Glu2009=
ENST00000505350.2:c.*5978_*5979delinsAG	ENSP00000481752.1:n.*5978_*5979delinsAG
ENST00000507379.6:c.5918_5919delinsAG	ENSP00000423224.2:p.Glu1973=
ENST00000509732.6:c.5972_5973delinsAG	ENSP00000426541.2:p.Glu1991=
ENST00000512211.7:c.5972_5973delinsAG	ENSP00000423828.3:p.Glu1991=
ENST00000257430.9:c.5972_5973delinsAG MANE Select	ENSP00000257430.4:p.Glu1991=
ENST00000257430.8:c.5972_5973delinsAG	ENSP00000257430.4:p.Glu1991=
ENST00000508376.6:c.5972_5973delinsAG	ENSP00000427089.2:p.Glu1991=
ENST00000508624.5:c.*5294_*5295delinsAG	ENSP00000424265.1:n.*5294_*5295delinsAG
ENST00000520401.1:c.230+12594_230+12595delinsAG
NM_000038.5:c.5972_5973delinsAG	NP_000029.2:p.Glu1991=
NM_001127510.2:c.5972_5973delinsAG	NP_001120982.1:p.Glu1991=
NM_001127511.2:c.5918_5919delinsAG	NP_001120983.2:p.Glu1973=
NM_001354895.1:c.5972_5973delinsAG	NP_001341824.1:p.Glu1991=
NM_001354896.1:c.6026_6027delinsAG	NP_001341825.1:p.Glu2009=
NM_001354897.1:c.6002_6003delinsAG	NP_001341826.1:p.Glu2001=
NM_001354898.1:c.5897_5898delinsAG	NP_001341827.1:p.Glu1966=
NM_001354899.1:c.5888_5889delinsAG	NP_001341828.1:p.Glu1963=
NM_001354900.1:c.5849_5850delinsAG	NP_001341829.1:p.Glu1950=
NM_001354901.1:c.5795_5796delinsAG	NP_001341830.1:p.Glu1932=
NM_001354902.1:c.5699_5700delinsAG	NP_001341831.1:p.Glu1900=
NM_001354903.1:c.5669_5670delinsAG	NP_001341832.1:p.Glu1890=
NM_001354904.1:c.5594_5595delinsAG	NP_001341833.1:p.Glu1865=
NM_001354905.1:c.5492_5493delinsAG	NP_001341834.1:p.Glu1831=
NM_001354906.1:c.5123_5124delinsAG	NP_001341835.1:p.Glu1708=
NM_000038.6:c.5972_5973delinsAG MANE Select	NP_000029.2:p.Glu1991=
NM_001127510.3:c.5972_5973delinsAG	NP_001120982.1:p.Glu1991=
NM_001127511.3:c.5918_5919delinsAG	NP_001120983.2:p.Glu1973=
NM_001354895.2:c.5972_5973delinsAG	NP_001341824.1:p.Glu1991=
NM_001354896.2:c.6026_6027delinsAG	NP_001341825.1:p.Glu2009=
NM_001354897.2:c.6002_6003delinsAG	NP_001341826.1:p.Glu2001=
NM_001354898.2:c.5897_5898delinsAG	NP_001341827.1:p.Glu1966=
NM_001354899.2:c.5888_5889delinsAG	NP_001341828.1:p.Glu1963=
NM_001354900.2:c.5849_5850delinsAG	NP_001341829.1:p.Glu1950=
NM_001354901.2:c.5795_5796delinsAG	NP_001341830.1:p.Glu1932=
NM_001354902.2:c.5699_5700delinsAG	NP_001341831.1:p.Glu1900=
NM_001354903.2:c.5669_5670delinsAG	NP_001341832.1:p.Glu1890=
NM_001354904.2:c.5594_5595delinsAG	NP_001341833.1:p.Glu1865=
NM_001354905.2:c.5492_5493delinsAG	NP_001341834.1:p.Glu1831=
NM_001354906.2:c.5123_5124delinsAG	NP_001341835.1:p.Glu1708=