Canonical Allele Identifier: CA1573497172

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821949_112821950delinsCT , CM000667.2:g.112821949_112821950delinsCT	GRCh38
NC_000005.9:g.112157646_112157647delinsCT , CM000667.1:g.112157646_112157647delinsCT	GRCh37
NC_000005.8:g.112185545_112185546delinsCT	NCBI36
NG_008481.4:g.134429_134430delinsCT , LRG_130:g.134429_134430delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1366_1367delinsCT	ENSP00000484935.2:p.Leu456=
ENST00000504915.3:c.1366_1367delinsCT	ENSP00000473355.2:p.Leu456=
ENST00000505084.2:n.1422_1423delinsCT
ENST00000505350.2:c.*1372_*1373delinsCT	ENSP00000481752.1:n.*1372_*1373delinsCT
ENST00000507379.6:c.1312_1313delinsCT	ENSP00000423224.2:p.Leu438=
ENST00000509732.6:c.1366_1367delinsCT	ENSP00000426541.2:p.Leu456=
ENST00000512211.7:c.1366_1367delinsCT	ENSP00000423828.3:p.Leu456=
ENST00000257430.9:c.1366_1367delinsCT MANE Select	ENSP00000257430.4:p.Leu456=
ENST00000257430.8:c.1366_1367delinsCT	ENSP00000257430.4:p.Leu456=
ENST00000502371.2:c.54_55delinsCT
ENST00000504915.2:c.1_2delinsCT	ENSP00000473355.1:p.Leu1=
ENST00000507379.5:c.1312_1313delinsCT	ENSP00000423224.1:p.Leu438=
ENST00000508376.6:c.1366_1367delinsCT	ENSP00000427089.2:p.Leu456=
ENST00000508624.5:c.*688_*689delinsCT	ENSP00000424265.1:n.*688_*689delinsCT
ENST00000512211.6:c.1366_1367delinsCT	ENSP00000423828.2:p.Leu456=
NM_000038.5:c.1366_1367delinsCT	NP_000029.2:p.Leu456=
NM_001127510.2:c.1366_1367delinsCT	NP_001120982.1:p.Leu456=
NM_001127511.2:c.1312_1313delinsCT	NP_001120983.2:p.Leu438=
NM_001354895.1:c.1366_1367delinsCT	NP_001341824.1:p.Leu456=
NM_001354896.1:c.1366_1367delinsCT	NP_001341825.1:p.Leu456=
NM_001354897.1:c.1396_1397delinsCT	NP_001341826.1:p.Leu466=
NM_001354898.1:c.1291_1292delinsCT	NP_001341827.1:p.Leu431=
NM_001354899.1:c.1282_1283delinsCT	NP_001341828.1:p.Leu428=
NM_001354900.1:c.1189_1190delinsCT	NP_001341829.1:p.Leu397=
NM_001354901.1:c.1189_1190delinsCT	NP_001341830.1:p.Leu397=
NM_001354902.1:c.1093_1094delinsCT	NP_001341831.1:p.Leu365=
NM_001354903.1:c.1063_1064delinsCT	NP_001341832.1:p.Leu355=
NM_001354904.1:c.988_989delinsCT	NP_001341833.1:p.Leu330=
NM_001354905.1:c.886_887delinsCT	NP_001341834.1:p.Leu296=
NM_001354906.1:c.517_518delinsCT	NP_001341835.1:p.Leu173=
NM_000038.6:c.1366_1367delinsCT MANE Select	NP_000029.2:p.Leu456=
NM_001127510.3:c.1366_1367delinsCT	NP_001120982.1:p.Leu456=
NM_001127511.3:c.1312_1313delinsCT	NP_001120983.2:p.Leu438=
NM_001354895.2:c.1366_1367delinsCT	NP_001341824.1:p.Leu456=
NM_001354896.2:c.1366_1367delinsCT	NP_001341825.1:p.Leu456=
NM_001354897.2:c.1396_1397delinsCT	NP_001341826.1:p.Leu466=
NM_001354898.2:c.1291_1292delinsCT	NP_001341827.1:p.Leu431=
NM_001354899.2:c.1282_1283delinsCT	NP_001341828.1:p.Leu428=
NM_001354900.2:c.1189_1190delinsCT	NP_001341829.1:p.Leu397=
NM_001354901.2:c.1189_1190delinsCT	NP_001341830.1:p.Leu397=
NM_001354902.2:c.1093_1094delinsCT	NP_001341831.1:p.Leu365=
NM_001354903.2:c.1063_1064delinsCT	NP_001341832.1:p.Leu355=
NM_001354904.2:c.988_989delinsCT	NP_001341833.1:p.Leu330=
NM_001354905.2:c.886_887delinsCT	NP_001341834.1:p.Leu296=
NM_001354906.2:c.517_518delinsCT	NP_001341835.1:p.Leu173=