Canonical Allele Identifier: CA2695205040

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835005_112835006del , CM000667.2:g.112835005_112835006del	GRCh38
NC_000005.9:g.112170702_112170703del , CM000667.1:g.112170702_112170703del	GRCh37
NC_000005.8:g.112198601_112198602del	NCBI36
NG_008481.4:g.147485_147486del , LRG_130:g.147485_147486del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1463_1464del	ENSP00000484935.2:p.His488LeufsTer10
ENST00000504915.3:c.1852_1853del	ENSP00000473355.2:p.Thr618Ter
ENST00000505350.2:c.*1804_*1805del	ENSP00000481752.1:n.*1804_*1805del
ENST00000507379.6:c.1744_1745del	ENSP00000423224.2:p.Thr582Ter
ENST00000509732.6:c.1798_1799del	ENSP00000426541.2:p.Thr600Ter
ENST00000512211.7:c.1798_1799del	ENSP00000423828.3:p.Thr600Ter
ENST00000257430.9:c.1798_1799del MANE Select	ENSP00000257430.4:p.Thr600Ter
ENST00000257430.8:c.1798_1799del	ENSP00000257430.4:p.Thr600Ter
ENST00000502371.2:c.151_152del
ENST00000504915.2:c.487_488del	ENSP00000473355.1:p.Thr163Ter
ENST00000507379.5:c.1744_1745del	ENSP00000423224.1:p.Thr582Ter
ENST00000508376.6:c.1798_1799del	ENSP00000427089.2:p.Thr600Ter
ENST00000508624.5:c.*1120_*1121del	ENSP00000424265.1:n.*1120_*1121del
ENST00000512211.6:c.1798_1799del	ENSP00000423828.2:p.Thr600Ter
ENST00000520401.1:c.230+6033_230+6034del
NM_000038.5:c.1798_1799del	NP_000029.2:p.Thr600Ter
NM_001127510.2:c.1798_1799del	NP_001120982.1:p.Thr600Ter
NM_001127511.2:c.1744_1745del	NP_001120983.2:p.Thr582Ter
NM_001354895.1:c.1798_1799del	NP_001341824.1:p.Thr600Ter
NM_001354896.1:c.1852_1853del	NP_001341825.1:p.Thr618Ter
NM_001354897.1:c.1828_1829del	NP_001341826.1:p.Thr610Ter
NM_001354898.1:c.1723_1724del	NP_001341827.1:p.Thr575Ter
NM_001354899.1:c.1714_1715del	NP_001341828.1:p.Thr572Ter
NM_001354900.1:c.1675_1676del	NP_001341829.1:p.Thr559Ter
NM_001354901.1:c.1621_1622del	NP_001341830.1:p.Thr541Ter
NM_001354902.1:c.1525_1526del	NP_001341831.1:p.Thr509Ter
NM_001354903.1:c.1495_1496del	NP_001341832.1:p.Thr499Ter
NM_001354904.1:c.1420_1421del	NP_001341833.1:p.Thr474Ter
NM_001354905.1:c.1318_1319del	NP_001341834.1:p.Thr440Ter
NM_001354906.1:c.949_950del	NP_001341835.1:p.Thr317Ter
NM_000038.6:c.1798_1799del MANE Select	NP_000029.2:p.Thr600Ter
NM_001127510.3:c.1798_1799del	NP_001120982.1:p.Thr600Ter
NM_001127511.3:c.1744_1745del	NP_001120983.2:p.Thr582Ter
NM_001354895.2:c.1798_1799del	NP_001341824.1:p.Thr600Ter
NM_001354896.2:c.1852_1853del	NP_001341825.1:p.Thr618Ter
NM_001354897.2:c.1828_1829del	NP_001341826.1:p.Thr610Ter
NM_001354898.2:c.1723_1724del	NP_001341827.1:p.Thr575Ter
NM_001354899.2:c.1714_1715del	NP_001341828.1:p.Thr572Ter
NM_001354900.2:c.1675_1676del	NP_001341829.1:p.Thr559Ter
NM_001354901.2:c.1621_1622del	NP_001341830.1:p.Thr541Ter
NM_001354902.2:c.1525_1526del	NP_001341831.1:p.Thr509Ter
NM_001354903.2:c.1495_1496del	NP_001341832.1:p.Thr499Ter
NM_001354904.2:c.1420_1421del	NP_001341833.1:p.Thr474Ter
NM_001354905.2:c.1318_1319del	NP_001341834.1:p.Thr440Ter
NM_001354906.2:c.949_950del	NP_001341835.1:p.Thr317Ter