Canonical Allele Identifier: CA1573505308

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827164_112827166delinsACT , CM000667.2:g.112827164_112827166delinsACT	GRCh38
NC_000005.9:g.112162861_112162863delinsACT , CM000667.1:g.112162861_112162863delinsACT	GRCh37
NC_000005.8:g.112190760_112190762delinsACT	NCBI36
NG_008481.4:g.139644_139646delinsACT , LRG_130:g.139644_139646delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5173_1408+5175delinsACT	ENSP00000484935.2:n.1408+5173_1408+5175de...
ENST00000504915.3:c.1519_1521delinsACT	ENSP00000473355.2:p.Thr507=
ENST00000505084.2:n.1521_1523delinsACT
ENST00000505350.2:c.*1471_*1473delinsACT	ENSP00000481752.1:n.*1471_*1473delinsACT
ENST00000507379.6:c.1411_1413delinsACT	ENSP00000423224.2:p.Thr471=
ENST00000509732.6:c.1465_1467delinsACT	ENSP00000426541.2:p.Thr489=
ENST00000512211.7:c.1465_1467delinsACT	ENSP00000423828.3:p.Thr489=
ENST00000257430.9:c.1465_1467delinsACT MANE Select	ENSP00000257430.4:p.Thr489=
ENST00000257430.8:c.1465_1467delinsACT	ENSP00000257430.4:p.Thr489=
ENST00000502371.2:c.96+5173_96+5175delinsACT
ENST00000504915.2:c.154_156delinsACT	ENSP00000473355.1:p.Thr52=
ENST00000507379.5:c.1411_1413delinsACT	ENSP00000423224.1:p.Thr471=
ENST00000508376.6:c.1465_1467delinsACT	ENSP00000427089.2:p.Thr489=
ENST00000508624.5:c.*787_*789delinsACT	ENSP00000424265.1:n.*787_*789delinsACT
ENST00000512211.6:c.1465_1467delinsACT	ENSP00000423828.2:p.Thr489=
NM_000038.5:c.1465_1467delinsACT	NP_000029.2:p.Thr489=
NM_001127510.2:c.1465_1467delinsACT	NP_001120982.1:p.Thr489=
NM_001127511.2:c.1411_1413delinsACT	NP_001120983.2:p.Thr471=
NM_001354895.1:c.1465_1467delinsACT	NP_001341824.1:p.Thr489=
NM_001354896.1:c.1519_1521delinsACT	NP_001341825.1:p.Thr507=
NM_001354897.1:c.1495_1497delinsACT	NP_001341826.1:p.Thr499=
NM_001354898.1:c.1390_1392delinsACT	NP_001341827.1:p.Thr464=
NM_001354899.1:c.1381_1383delinsACT	NP_001341828.1:p.Thr461=
NM_001354900.1:c.1342_1344delinsACT	NP_001341829.1:p.Thr448=
NM_001354901.1:c.1288_1290delinsACT	NP_001341830.1:p.Thr430=
NM_001354902.1:c.1192_1194delinsACT	NP_001341831.1:p.Thr398=
NM_001354903.1:c.1162_1164delinsACT	NP_001341832.1:p.Thr388=
NM_001354904.1:c.1087_1089delinsACT	NP_001341833.1:p.Thr363=
NM_001354905.1:c.985_987delinsACT	NP_001341834.1:p.Thr329=
NM_001354906.1:c.616_618delinsACT	NP_001341835.1:p.Thr206=
NM_000038.6:c.1465_1467delinsACT MANE Select	NP_000029.2:p.Thr489=
NM_001127510.3:c.1465_1467delinsACT	NP_001120982.1:p.Thr489=
NM_001127511.3:c.1411_1413delinsACT	NP_001120983.2:p.Thr471=
NM_001354895.2:c.1465_1467delinsACT	NP_001341824.1:p.Thr489=
NM_001354896.2:c.1519_1521delinsACT	NP_001341825.1:p.Thr507=
NM_001354897.2:c.1495_1497delinsACT	NP_001341826.1:p.Thr499=
NM_001354898.2:c.1390_1392delinsACT	NP_001341827.1:p.Thr464=
NM_001354899.2:c.1381_1383delinsACT	NP_001341828.1:p.Thr461=
NM_001354900.2:c.1342_1344delinsACT	NP_001341829.1:p.Thr448=
NM_001354901.2:c.1288_1290delinsACT	NP_001341830.1:p.Thr430=
NM_001354902.2:c.1192_1194delinsACT	NP_001341831.1:p.Thr398=
NM_001354903.2:c.1162_1164delinsACT	NP_001341832.1:p.Thr388=
NM_001354904.2:c.1087_1089delinsACT	NP_001341833.1:p.Thr363=
NM_001354905.2:c.985_987delinsACT	NP_001341834.1:p.Thr329=
NM_001354906.2:c.616_618delinsACT	NP_001341835.1:p.Thr206=