Canonical Allele Identifier: CA1573508672

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828884_112828885delinsCT , CM000667.2:g.112828884_112828885delinsCT	GRCh38
NC_000005.9:g.112164581_112164582delinsCT , CM000667.1:g.112164581_112164582delinsCT	GRCh37
NC_000005.8:g.112192480_112192481delinsCT	NCBI36
NG_008481.4:g.141364_141365delinsCT , LRG_130:g.141364_141365delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6067_1409-6066delinsCT	ENSP00000484935.2:n.1409-6067_1409-6066de...
ENST00000504915.3:c.1709_1710delinsCT	ENSP00000473355.2:p.Ser570=
ENST00000505084.2:n.1711_1712delinsCT
ENST00000505350.2:c.*1661_*1662delinsCT	ENSP00000481752.1:n.*1661_*1662delinsCT
ENST00000507379.6:c.1601_1602delinsCT	ENSP00000423224.2:p.Ser534=
ENST00000509732.6:c.1655_1656delinsCT	ENSP00000426541.2:p.Ser552=
ENST00000512211.7:c.1655_1656delinsCT	ENSP00000423828.3:p.Ser552=
ENST00000257430.9:c.1655_1656delinsCT MANE Select	ENSP00000257430.4:p.Ser552=
ENST00000257430.8:c.1655_1656delinsCT	ENSP00000257430.4:p.Ser552=
ENST00000502371.2:c.97-6067_97-6066delinsCT
ENST00000504915.2:c.344_345delinsCT	ENSP00000473355.1:p.Ser115=
ENST00000505084.1:n.142_143delinsCT
ENST00000507379.5:c.1601_1602delinsCT	ENSP00000423224.1:p.Ser534=
ENST00000508376.6:c.1655_1656delinsCT	ENSP00000427089.2:p.Ser552=
ENST00000508624.5:c.*977_*978delinsCT	ENSP00000424265.1:n.*977_*978delinsCT
ENST00000512211.6:c.1655_1656delinsCT	ENSP00000423828.2:p.Ser552=
ENST00000520401.1:c.142_143delinsCT
NM_000038.5:c.1655_1656delinsCT	NP_000029.2:p.Ser552=
NM_001127510.2:c.1655_1656delinsCT	NP_001120982.1:p.Ser552=
NM_001127511.2:c.1601_1602delinsCT	NP_001120983.2:p.Ser534=
NM_001354895.1:c.1655_1656delinsCT	NP_001341824.1:p.Ser552=
NM_001354896.1:c.1709_1710delinsCT	NP_001341825.1:p.Ser570=
NM_001354897.1:c.1685_1686delinsCT	NP_001341826.1:p.Ser562=
NM_001354898.1:c.1580_1581delinsCT	NP_001341827.1:p.Ser527=
NM_001354899.1:c.1571_1572delinsCT	NP_001341828.1:p.Ser524=
NM_001354900.1:c.1532_1533delinsCT	NP_001341829.1:p.Ser511=
NM_001354901.1:c.1478_1479delinsCT	NP_001341830.1:p.Ser493=
NM_001354902.1:c.1382_1383delinsCT	NP_001341831.1:p.Ser461=
NM_001354903.1:c.1352_1353delinsCT	NP_001341832.1:p.Ser451=
NM_001354904.1:c.1277_1278delinsCT	NP_001341833.1:p.Ser426=
NM_001354905.1:c.1175_1176delinsCT	NP_001341834.1:p.Ser392=
NM_001354906.1:c.806_807delinsCT	NP_001341835.1:p.Ser269=
NM_000038.6:c.1655_1656delinsCT MANE Select	NP_000029.2:p.Ser552=
NM_001127510.3:c.1655_1656delinsCT	NP_001120982.1:p.Ser552=
NM_001127511.3:c.1601_1602delinsCT	NP_001120983.2:p.Ser534=
NM_001354895.2:c.1655_1656delinsCT	NP_001341824.1:p.Ser552=
NM_001354896.2:c.1709_1710delinsCT	NP_001341825.1:p.Ser570=
NM_001354897.2:c.1685_1686delinsCT	NP_001341826.1:p.Ser562=
NM_001354898.2:c.1580_1581delinsCT	NP_001341827.1:p.Ser527=
NM_001354899.2:c.1571_1572delinsCT	NP_001341828.1:p.Ser524=
NM_001354900.2:c.1532_1533delinsCT	NP_001341829.1:p.Ser511=
NM_001354901.2:c.1478_1479delinsCT	NP_001341830.1:p.Ser493=
NM_001354902.2:c.1382_1383delinsCT	NP_001341831.1:p.Ser461=
NM_001354903.2:c.1352_1353delinsCT	NP_001341832.1:p.Ser451=
NM_001354904.2:c.1277_1278delinsCT	NP_001341833.1:p.Ser426=
NM_001354905.2:c.1175_1176delinsCT	NP_001341834.1:p.Ser392=
NM_001354906.2:c.806_807delinsCT	NP_001341835.1:p.Ser269=