Canonical Allele Identifier: CA350460

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841420_112841423del , CM000667.2:g.112841420_112841423del	GRCh38
NC_000005.9:g.112177117_112177120del , CM000667.1:g.112177117_112177120del	GRCh37
NC_000005.8:g.112205016_112205019del	NCBI36
NG_008481.4:g.153900_153903del , LRG_130:g.153900_153903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5880_5883del	ENSP00000473355.2:p.Asp1960GlufsTer27
ENST00000505350.2:c.*5832_*5835del	ENSP00000481752.1:n.*5832_*5835del
ENST00000507379.6:c.5772_5775del	ENSP00000423224.2:p.Asp1924GlufsTer27
ENST00000509732.6:c.5826_5829del	ENSP00000426541.2:p.Asp1942GlufsTer27
ENST00000512211.7:c.5826_5829del	ENSP00000423828.3:p.Asp1942GlufsTer27
ENST00000257430.9:c.5826_5829del MANE Select	ENSP00000257430.4:p.Asp1942GlufsTer27
ENST00000257430.8:c.5826_5829del	ENSP00000257430.4:p.Asp1942GlufsTer27
ENST00000508376.6:c.5826_5829del	ENSP00000427089.2:p.Asp1942GlufsTer27
ENST00000508624.5:c.*5148_*5151del	ENSP00000424265.1:n.*5148_*5151del
ENST00000520401.1:c.230+12448_230+12451del
NM_000038.5:c.5826_5829del	NP_000029.2:p.Asp1942GlufsTer27
NM_001127510.2:c.5826_5829del	NP_001120982.1:p.Asp1942GlufsTer27
NM_001127511.2:c.5772_5775del	NP_001120983.2:p.Asp1924GlufsTer27
NM_001354895.1:c.5826_5829del	NP_001341824.1:p.Asp1942GlufsTer27
NM_001354896.1:c.5880_5883del	NP_001341825.1:p.Asp1960GlufsTer27
NM_001354897.1:c.5856_5859del	NP_001341826.1:p.Asp1952GlufsTer27
NM_001354898.1:c.5751_5754del	NP_001341827.1:p.Asp1917GlufsTer27
NM_001354899.1:c.5742_5745del	NP_001341828.1:p.Asp1914GlufsTer27
NM_001354900.1:c.5703_5706del	NP_001341829.1:p.Asp1901GlufsTer27
NM_001354901.1:c.5649_5652del	NP_001341830.1:p.Asp1883GlufsTer27
NM_001354902.1:c.5553_5556del	NP_001341831.1:p.Asp1851GlufsTer27
NM_001354903.1:c.5523_5526del	NP_001341832.1:p.Asp1841GlufsTer27
NM_001354904.1:c.5448_5451del	NP_001341833.1:p.Asp1816GlufsTer27
NM_001354905.1:c.5346_5349del	NP_001341834.1:p.Asp1782GlufsTer27
NM_001354906.1:c.4977_4980del	NP_001341835.1:p.Asp1659GlufsTer27
NM_000038.6:c.5826_5829del MANE Select	NP_000029.2:p.Asp1942GlufsTer27
NM_001127510.3:c.5826_5829del	NP_001120982.1:p.Asp1942GlufsTer27
NM_001127511.3:c.5772_5775del	NP_001120983.2:p.Asp1924GlufsTer27
NM_001354895.2:c.5826_5829del	NP_001341824.1:p.Asp1942GlufsTer27
NM_001354896.2:c.5880_5883del	NP_001341825.1:p.Asp1960GlufsTer27
NM_001354897.2:c.5856_5859del	NP_001341826.1:p.Asp1952GlufsTer27
NM_001354898.2:c.5751_5754del	NP_001341827.1:p.Asp1917GlufsTer27
NM_001354899.2:c.5742_5745del	NP_001341828.1:p.Asp1914GlufsTer27
NM_001354900.2:c.5703_5706del	NP_001341829.1:p.Asp1901GlufsTer27
NM_001354901.2:c.5649_5652del	NP_001341830.1:p.Asp1883GlufsTer27
NM_001354902.2:c.5553_5556del	NP_001341831.1:p.Asp1851GlufsTer27
NM_001354903.2:c.5523_5526del	NP_001341832.1:p.Asp1841GlufsTer27
NM_001354904.2:c.5448_5451del	NP_001341833.1:p.Asp1816GlufsTer27
NM_001354905.2:c.5346_5349del	NP_001341834.1:p.Asp1782GlufsTer27
NM_001354906.2:c.4977_4980del	NP_001341835.1:p.Asp1659GlufsTer27