Canonical Allele Identifier: CA1573470948

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835058_112835074delinsTGGCACTCTTACTTACC , CM000667.2:g.112835058_112835074delinsTGGCACTCTTACTTACC	GRCh38
NC_000005.9:g.112170755_112170771delinsTGGCACTCTTACTTACC , CM000667.1:g.112170755_112170771delinsTGGCACTCTTACTTACC	GRCh37
NC_000005.8:g.112198654_112198670delinsTGGCACTCTTACTTACC	NCBI36
NG_008481.4:g.147538_147554delinsTGGCACTCTTACTTACC , LRG_130:g.147538_147554delinsTGGCACTCTTACTTACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1516_1532delinsTGGCACTCTTACTTACC	ENSP00000484935.2:n.1516_1532delinsTGGCAC...
ENST00000504915.3:c.1905_1921delinsTGGCACTCTTACTTACC	ENSP00000473355.2:p.Val635=
ENST00000505350.2:c.*1857_*1873delinsTGGCACTCTTACTTACC	ENSP00000481752.1:n.*1857_*1873delinsTGGC...
ENST00000507379.6:c.1797_1813delinsTGGCACTCTTACTTACC	ENSP00000423224.2:p.Val599=
ENST00000509732.6:c.1851_1867delinsTGGCACTCTTACTTACC	ENSP00000426541.2:p.Val617=
ENST00000512211.7:c.1851_1867delinsTGGCACTCTTACTTACC	ENSP00000423828.3:p.Val617=
ENST00000257430.9:c.1851_1867delinsTGGCACTCTTACTTACC MANE Select	ENSP00000257430.4:p.Val617=
ENST00000257430.8:c.1851_1867delinsTGGCACTCTTACTTACC	ENSP00000257430.4:p.Val617=
ENST00000502371.2:c.204_220delinsTGGCACTCTTACTTACC
ENST00000504915.2:c.540_556delinsTGGCACTCTTACTTACC	ENSP00000473355.1:p.Val180=
ENST00000507379.5:c.1797_1813delinsTGGCACTCTTACTTACC	ENSP00000423224.1:p.Val599=
ENST00000508376.6:c.1851_1867delinsTGGCACTCTTACTTACC	ENSP00000427089.2:p.Val617=
ENST00000508624.5:c.*1173_*1189delinsTGGCACTCTTACTTACC	ENSP00000424265.1:n.*1173_*1189delinsTGGC...
ENST00000512211.6:c.1851_1867delinsTGGCACTCTTACTTACC	ENSP00000423828.2:p.Val617=
ENST00000520401.1:c.230+6086_230+6102delinsTGGCACTCTTACTTACC
NM_000038.5:c.1851_1867delinsTGGCACTCTTACTTACC	NP_000029.2:p.Val617=
NM_001127510.2:c.1851_1867delinsTGGCACTCTTACTTACC	NP_001120982.1:p.Val617=
NM_001127511.2:c.1797_1813delinsTGGCACTCTTACTTACC	NP_001120983.2:p.Val599=
NM_001354895.1:c.1851_1867delinsTGGCACTCTTACTTACC	NP_001341824.1:p.Val617=
NM_001354896.1:c.1905_1921delinsTGGCACTCTTACTTACC	NP_001341825.1:p.Val635=
NM_001354897.1:c.1881_1897delinsTGGCACTCTTACTTACC	NP_001341826.1:p.Val627=
NM_001354898.1:c.1776_1792delinsTGGCACTCTTACTTACC	NP_001341827.1:p.Val592=
NM_001354899.1:c.1767_1783delinsTGGCACTCTTACTTACC	NP_001341828.1:p.Val589=
NM_001354900.1:c.1728_1744delinsTGGCACTCTTACTTACC	NP_001341829.1:p.Val576=
NM_001354901.1:c.1674_1690delinsTGGCACTCTTACTTACC	NP_001341830.1:p.Val558=
NM_001354902.1:c.1578_1594delinsTGGCACTCTTACTTACC	NP_001341831.1:p.Val526=
NM_001354903.1:c.1548_1564delinsTGGCACTCTTACTTACC	NP_001341832.1:p.Val516=
NM_001354904.1:c.1473_1489delinsTGGCACTCTTACTTACC	NP_001341833.1:p.Val491=
NM_001354905.1:c.1371_1387delinsTGGCACTCTTACTTACC	NP_001341834.1:p.Val457=
NM_001354906.1:c.1002_1018delinsTGGCACTCTTACTTACC	NP_001341835.1:p.Val334=
NM_000038.6:c.1851_1867delinsTGGCACTCTTACTTACC MANE Select	NP_000029.2:p.Val617=
NM_001127510.3:c.1851_1867delinsTGGCACTCTTACTTACC	NP_001120982.1:p.Val617=
NM_001127511.3:c.1797_1813delinsTGGCACTCTTACTTACC	NP_001120983.2:p.Val599=
NM_001354895.2:c.1851_1867delinsTGGCACTCTTACTTACC	NP_001341824.1:p.Val617=
NM_001354896.2:c.1905_1921delinsTGGCACTCTTACTTACC	NP_001341825.1:p.Val635=
NM_001354897.2:c.1881_1897delinsTGGCACTCTTACTTACC	NP_001341826.1:p.Val627=
NM_001354898.2:c.1776_1792delinsTGGCACTCTTACTTACC	NP_001341827.1:p.Val592=
NM_001354899.2:c.1767_1783delinsTGGCACTCTTACTTACC	NP_001341828.1:p.Val589=
NM_001354900.2:c.1728_1744delinsTGGCACTCTTACTTACC	NP_001341829.1:p.Val576=
NM_001354901.2:c.1674_1690delinsTGGCACTCTTACTTACC	NP_001341830.1:p.Val558=
NM_001354902.2:c.1578_1594delinsTGGCACTCTTACTTACC	NP_001341831.1:p.Val526=
NM_001354903.2:c.1548_1564delinsTGGCACTCTTACTTACC	NP_001341832.1:p.Val516=
NM_001354904.2:c.1473_1489delinsTGGCACTCTTACTTACC	NP_001341833.1:p.Val491=
NM_001354905.2:c.1371_1387delinsTGGCACTCTTACTTACC	NP_001341834.1:p.Val457=
NM_001354906.2:c.1002_1018delinsTGGCACTCTTACTTACC	NP_001341835.1:p.Val334=