Canonical Allele Identifier: CA658760782

Gene: APC

Linked Data

• PubMed: PMID:20223039

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840335dup , CM000667.2:g.112840335dup	GRCh38
NC_000005.9:g.112176032dup , CM000667.1:g.112176032dup	GRCh37
NC_000005.8:g.112203931dup	NCBI36
NG_008481.4:g.152815dup , LRG_130:g.152815dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4795dup	ENSP00000473355.2:p.Ser1599PhefsTer10
ENST00000505350.2:c.*4747dup	ENSP00000481752.1:n.*4747dup
ENST00000507379.6:c.4687dup	ENSP00000423224.2:p.Ser1563PhefsTer10
ENST00000509732.6:c.4741dup	ENSP00000426541.2:p.Ser1581PhefsTer10
ENST00000512211.7:c.4741dup	ENSP00000423828.3:p.Ser1581PhefsTer10
ENST00000257430.9:c.4741dup MANE Select	ENSP00000257430.4:p.Ser1581PhefsTer10
ENST00000257430.8:c.4741dup	ENSP00000257430.4:p.Ser1581PhefsTer10
ENST00000508376.6:c.4741dup	ENSP00000427089.2:p.Ser1581PhefsTer10
ENST00000508624.5:c.*4063dup	ENSP00000424265.1:n.*4063dup
ENST00000520401.1:c.230+11363dup
NM_000038.5:c.4741dup	NP_000029.2:p.Ser1581PhefsTer10
NM_001127510.2:c.4741dup	NP_001120982.1:p.Ser1581PhefsTer10
NM_001127511.2:c.4687dup	NP_001120983.2:p.Ser1563PhefsTer10
NM_001354895.1:c.4741dup	NP_001341824.1:p.Ser1581PhefsTer10
NM_001354896.1:c.4795dup	NP_001341825.1:p.Ser1599PhefsTer10
NM_001354897.1:c.4771dup	NP_001341826.1:p.Ser1591PhefsTer10
NM_001354898.1:c.4666dup	NP_001341827.1:p.Ser1556PhefsTer10
NM_001354899.1:c.4657dup	NP_001341828.1:p.Ser1553PhefsTer10
NM_001354900.1:c.4618dup	NP_001341829.1:p.Ser1540PhefsTer10
NM_001354901.1:c.4564dup	NP_001341830.1:p.Ser1522PhefsTer10
NM_001354902.1:c.4468dup	NP_001341831.1:p.Ser1490PhefsTer10
NM_001354903.1:c.4438dup	NP_001341832.1:p.Ser1480PhefsTer10
NM_001354904.1:c.4363dup	NP_001341833.1:p.Ser1455PhefsTer10
NM_001354905.1:c.4261dup	NP_001341834.1:p.Ser1421PhefsTer10
NM_001354906.1:c.3892dup	NP_001341835.1:p.Ser1298PhefsTer10
NM_000038.6:c.4741dup MANE Select	NP_000029.2:p.Ser1581PhefsTer10
NM_001127510.3:c.4741dup	NP_001120982.1:p.Ser1581PhefsTer10
NM_001127511.3:c.4687dup	NP_001120983.2:p.Ser1563PhefsTer10
NM_001354895.2:c.4741dup	NP_001341824.1:p.Ser1581PhefsTer10
NM_001354896.2:c.4795dup	NP_001341825.1:p.Ser1599PhefsTer10
NM_001354897.2:c.4771dup	NP_001341826.1:p.Ser1591PhefsTer10
NM_001354898.2:c.4666dup	NP_001341827.1:p.Ser1556PhefsTer10
NM_001354899.2:c.4657dup	NP_001341828.1:p.Ser1553PhefsTer10
NM_001354900.2:c.4618dup	NP_001341829.1:p.Ser1540PhefsTer10
NM_001354901.2:c.4564dup	NP_001341830.1:p.Ser1522PhefsTer10
NM_001354902.2:c.4468dup	NP_001341831.1:p.Ser1490PhefsTer10
NM_001354903.2:c.4438dup	NP_001341832.1:p.Ser1480PhefsTer10
NM_001354904.2:c.4363dup	NP_001341833.1:p.Ser1455PhefsTer10
NM_001354905.2:c.4261dup	NP_001341834.1:p.Ser1421PhefsTer10
NM_001354906.2:c.3892dup	NP_001341835.1:p.Ser1298PhefsTer10