Canonical Allele Identifier: CA2582341280

Gene: APC

Linked Data

• ClinVar Variation Id: 2583643
• ClinVar RCV Id: RCV003337493

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815553_112815556del , CM000667.2:g.112815553_112815556del	GRCh38
NC_000005.9:g.112151250_112151253del , CM000667.1:g.112151250_112151253del	GRCh37
NC_000005.8:g.112179149_112179152del	NCBI36
NG_008481.4:g.128033_128036del , LRG_130:g.128033_128036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.893_896del	ENSP00000484935.2:p.His298LeufsTer6
ENST00000504915.3:c.893_896del	ENSP00000473355.2:p.His298LeufsTer6
ENST00000505084.2:n.949_952del
ENST00000505350.2:c.*899_*902del	ENSP00000481752.1:n.*899_*902del
ENST00000507379.6:c.839_842del	ENSP00000423224.2:p.His280LeufsTer6
ENST00000509732.6:c.893_896del	ENSP00000426541.2:p.His298LeufsTer6
ENST00000512211.7:c.893_896del	ENSP00000423828.3:p.His298LeufsTer6
ENST00000257430.9:c.893_896del MANE Select	ENSP00000257430.4:p.His298LeufsTer6
ENST00000257430.8:c.893_896del	ENSP00000257430.4:p.His298LeufsTer6
ENST00000507379.5:c.839_842del	ENSP00000423224.1:p.His280LeufsTer6
ENST00000508376.6:c.893_896del	ENSP00000427089.2:p.His298LeufsTer6
ENST00000508624.5:c.*215_*218del	ENSP00000424265.1:n.*215_*218del
ENST00000512211.6:c.893_896del	ENSP00000423828.2:p.His298LeufsTer6
NM_000038.5:c.893_896del	NP_000029.2:p.His298LeufsTer6
NM_001127510.2:c.893_896del	NP_001120982.1:p.His298LeufsTer6
NM_001127511.2:c.839_842del	NP_001120983.2:p.His280LeufsTer6
NM_001354895.1:c.893_896del	NP_001341824.1:p.His298LeufsTer6
NM_001354896.1:c.893_896del	NP_001341825.1:p.His298LeufsTer6
NM_001354897.1:c.923_926del	NP_001341826.1:p.His308LeufsTer6
NM_001354898.1:c.818_821del	NP_001341827.1:p.His273LeufsTer6
NM_001354899.1:c.809_812del	NP_001341828.1:p.His270LeufsTer6
NM_001354900.1:c.716_719del	NP_001341829.1:p.His239LeufsTer6
NM_001354901.1:c.716_719del	NP_001341830.1:p.His239LeufsTer6
NM_001354902.1:c.923_926del	NP_001341831.1:p.His308LeufsTer6
NM_001354903.1:c.893_896del	NP_001341832.1:p.His298LeufsTer6
NM_001354904.1:c.818_821del	NP_001341833.1:p.His273LeufsTer6
NM_001354905.1:c.716_719del	NP_001341834.1:p.His239LeufsTer6
NM_001354906.1:c.44_47del	NP_001341835.1:p.His15LeufsTer6
NM_000038.6:c.893_896del MANE Select	NP_000029.2:p.His298LeufsTer6
NM_001127510.3:c.893_896del	NP_001120982.1:p.His298LeufsTer6
NM_001127511.3:c.839_842del	NP_001120983.2:p.His280LeufsTer6
NM_001354895.2:c.893_896del	NP_001341824.1:p.His298LeufsTer6
NM_001354896.2:c.893_896del	NP_001341825.1:p.His298LeufsTer6
NM_001354897.2:c.923_926del	NP_001341826.1:p.His308LeufsTer6
NM_001354898.2:c.818_821del	NP_001341827.1:p.His273LeufsTer6
NM_001354899.2:c.809_812del	NP_001341828.1:p.His270LeufsTer6
NM_001354900.2:c.716_719del	NP_001341829.1:p.His239LeufsTer6
NM_001354901.2:c.716_719del	NP_001341830.1:p.His239LeufsTer6
NM_001354902.2:c.923_926del	NP_001341831.1:p.His308LeufsTer6
NM_001354903.2:c.893_896del	NP_001341832.1:p.His298LeufsTer6
NM_001354904.2:c.818_821del	NP_001341833.1:p.His273LeufsTer6
NM_001354905.2:c.716_719del	NP_001341834.1:p.His239LeufsTer6
NM_001354906.2:c.44_47del	NP_001341835.1:p.His15LeufsTer6