Canonical Allele Identifier: CA1573470545

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840252_112840260delinsCAGAAAAAA , CM000667.2:g.112840252_112840260delinsCAGAAAAAA	GRCh38
NC_000005.9:g.112175949_112175957delinsCAGAAAAAA , CM000667.1:g.112175949_112175957delinsCAGAAAAAA	GRCh37
NC_000005.8:g.112203848_112203856delinsCAGAAAAAA	NCBI36
NG_008481.4:g.152732_152740delinsCAGAAAAAA , LRG_130:g.152732_152740delinsCAGAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4712_4720delinsCAGAAAAAA	ENSP00000473355.2:p.Ala1571=
ENST00000505350.2:c.*4664_*4672delinsCAGAAAAAA	ENSP00000481752.1:n.*4664_*4672delinsCAGAAAAAA
ENST00000507379.6:c.4604_4612delinsCAGAAAAAA	ENSP00000423224.2:p.Ala1535=
ENST00000509732.6:c.4658_4666delinsCAGAAAAAA	ENSP00000426541.2:p.Ala1553=
ENST00000512211.7:c.4658_4666delinsCAGAAAAAA	ENSP00000423828.3:p.Ala1553=
ENST00000257430.9:c.4658_4666delinsCAGAAAAAA MANE Select	ENSP00000257430.4:p.Ala1553=
ENST00000257430.8:c.4658_4666delinsCAGAAAAAA	ENSP00000257430.4:p.Ala1553=
ENST00000508376.6:c.4658_4666delinsCAGAAAAAA	ENSP00000427089.2:p.Ala1553=
ENST00000508624.5:c.*3980_*3988delinsCAGAAAAAA	ENSP00000424265.1:n.*3980_*3988delinsCAGAAAAAA
ENST00000520401.1:c.230+11280_230+11288delinsCAGAAAAAA
NM_000038.5:c.4658_4666delinsCAGAAAAAA	NP_000029.2:p.Ala1553=
NM_001127510.2:c.4658_4666delinsCAGAAAAAA	NP_001120982.1:p.Ala1553=
NM_001127511.2:c.4604_4612delinsCAGAAAAAA	NP_001120983.2:p.Ala1535=
NM_001354895.1:c.4658_4666delinsCAGAAAAAA	NP_001341824.1:p.Ala1553=
NM_001354896.1:c.4712_4720delinsCAGAAAAAA	NP_001341825.1:p.Ala1571=
NM_001354897.1:c.4688_4696delinsCAGAAAAAA	NP_001341826.1:p.Ala1563=
NM_001354898.1:c.4583_4591delinsCAGAAAAAA	NP_001341827.1:p.Ala1528=
NM_001354899.1:c.4574_4582delinsCAGAAAAAA	NP_001341828.1:p.Ala1525=
NM_001354900.1:c.4535_4543delinsCAGAAAAAA	NP_001341829.1:p.Ala1512=
NM_001354901.1:c.4481_4489delinsCAGAAAAAA	NP_001341830.1:p.Ala1494=
NM_001354902.1:c.4385_4393delinsCAGAAAAAA	NP_001341831.1:p.Ala1462=
NM_001354903.1:c.4355_4363delinsCAGAAAAAA	NP_001341832.1:p.Ala1452=
NM_001354904.1:c.4280_4288delinsCAGAAAAAA	NP_001341833.1:p.Ala1427=
NM_001354905.1:c.4178_4186delinsCAGAAAAAA	NP_001341834.1:p.Ala1393=
NM_001354906.1:c.3809_3817delinsCAGAAAAAA	NP_001341835.1:p.Ala1270=
NM_000038.6:c.4658_4666delinsCAGAAAAAA MANE Select	NP_000029.2:p.Ala1553=
NM_001127510.3:c.4658_4666delinsCAGAAAAAA	NP_001120982.1:p.Ala1553=
NM_001127511.3:c.4604_4612delinsCAGAAAAAA	NP_001120983.2:p.Ala1535=
NM_001354895.2:c.4658_4666delinsCAGAAAAAA	NP_001341824.1:p.Ala1553=
NM_001354896.2:c.4712_4720delinsCAGAAAAAA	NP_001341825.1:p.Ala1571=
NM_001354897.2:c.4688_4696delinsCAGAAAAAA	NP_001341826.1:p.Ala1563=
NM_001354898.2:c.4583_4591delinsCAGAAAAAA	NP_001341827.1:p.Ala1528=
NM_001354899.2:c.4574_4582delinsCAGAAAAAA	NP_001341828.1:p.Ala1525=
NM_001354900.2:c.4535_4543delinsCAGAAAAAA	NP_001341829.1:p.Ala1512=
NM_001354901.2:c.4481_4489delinsCAGAAAAAA	NP_001341830.1:p.Ala1494=
NM_001354902.2:c.4385_4393delinsCAGAAAAAA	NP_001341831.1:p.Ala1462=
NM_001354903.2:c.4355_4363delinsCAGAAAAAA	NP_001341832.1:p.Ala1452=
NM_001354904.2:c.4280_4288delinsCAGAAAAAA	NP_001341833.1:p.Ala1427=
NM_001354905.2:c.4178_4186delinsCAGAAAAAA	NP_001341834.1:p.Ala1393=
NM_001354906.2:c.3809_3817delinsCAGAAAAAA	NP_001341835.1:p.Ala1270=