Canonical Allele Identifier: CA2580612764

Gene: APC

Linked Data

• ClinVar Variation Id: 1562950
• ClinVar RCV Id: RCV003773722
• dbSNP Id: rs2149764235

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815602_112815604del , CM000667.2:g.112815602_112815604del	GRCh38
NC_000005.9:g.112151299_112151301del , CM000667.1:g.112151299_112151301del	GRCh37
NC_000005.8:g.112179198_112179200del	NCBI36
NG_008481.4:g.128082_128084del , LRG_130:g.128082_128084del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.933+9_933+11del	ENSP00000484935.2:n.933+9_933+11del
ENST00000504915.3:c.933+9_933+11del	ENSP00000473355.2:n.933+9_933+11del
ENST00000505084.2:n.989+9_989+11del
ENST00000505350.2:c.*939+9_*939+11del	ENSP00000481752.1:n.*939+9_*939+11del
ENST00000507379.6:c.879+9_879+11del	ENSP00000423224.2:n.879+9_879+11del
ENST00000509732.6:c.933+9_933+11del	ENSP00000426541.2:n.933+9_933+11del
ENST00000512211.7:c.933+9_933+11del	ENSP00000423828.3:n.933+9_933+11del
ENST00000257430.9:c.933+9_933+11del MANE Select	ENSP00000257430.4:n.933+9_933+11del
ENST00000257430.8:c.933+9_933+11del	ENSP00000257430.4:n.933+9_933+11del
ENST00000507379.5:c.879+9_879+11del	ENSP00000423224.1:n.879+9_879+11del
ENST00000508376.6:c.933+9_933+11del	ENSP00000427089.2:n.933+9_933+11del
ENST00000508624.5:c.*255+9_*255+11del	ENSP00000424265.1:n.*255+9_*255+11del
ENST00000512211.6:c.933+9_933+11del	ENSP00000423828.2:n.933+9_933+11del
NM_000038.5:c.933+9_933+11del	NP_000029.2:n.933+9_933+11del
NM_001127510.2:c.933+9_933+11del	NP_001120982.1:n.933+9_933+11del
NM_001127511.2:c.879+9_879+11del	NP_001120983.2:n.879+9_879+11del
NM_001354895.1:c.933+9_933+11del	NP_001341824.1:n.933+9_933+11del
NM_001354896.1:c.933+9_933+11del	NP_001341825.1:n.933+9_933+11del
NM_001354897.1:c.963+9_963+11del	NP_001341826.1:n.963+9_963+11del
NM_001354898.1:c.858+9_858+11del	NP_001341827.1:n.858+9_858+11del
NM_001354899.1:c.849+9_849+11del	NP_001341828.1:n.849+9_849+11del
NM_001354900.1:c.756+9_756+11del	NP_001341829.1:n.756+9_756+11del
NM_001354901.1:c.756+9_756+11del	NP_001341830.1:n.756+9_756+11del
NM_001354902.1:c.963+9_963+11del	NP_001341831.1:n.963+9_963+11del
NM_001354903.1:c.933+9_933+11del	NP_001341832.1:n.933+9_933+11del
NM_001354904.1:c.858+9_858+11del	NP_001341833.1:n.858+9_858+11del
NM_001354905.1:c.756+9_756+11del	NP_001341834.1:n.756+9_756+11del
NM_001354906.1:c.84+9_84+11del	NP_001341835.1:n.84+9_84+11del
NM_000038.6:c.933+9_933+11del MANE Select	NP_000029.2:n.933+9_933+11del
NM_001127510.3:c.933+9_933+11del	NP_001120982.1:n.933+9_933+11del
NM_001127511.3:c.879+9_879+11del	NP_001120983.2:n.879+9_879+11del
NM_001354895.2:c.933+9_933+11del	NP_001341824.1:n.933+9_933+11del
NM_001354896.2:c.933+9_933+11del	NP_001341825.1:n.933+9_933+11del
NM_001354897.2:c.963+9_963+11del	NP_001341826.1:n.963+9_963+11del
NM_001354898.2:c.858+9_858+11del	NP_001341827.1:n.858+9_858+11del
NM_001354899.2:c.849+9_849+11del	NP_001341828.1:n.849+9_849+11del
NM_001354900.2:c.756+9_756+11del	NP_001341829.1:n.756+9_756+11del
NM_001354901.2:c.756+9_756+11del	NP_001341830.1:n.756+9_756+11del
NM_001354902.2:c.963+9_963+11del	NP_001341831.1:n.963+9_963+11del
NM_001354903.2:c.933+9_933+11del	NP_001341832.1:n.933+9_933+11del
NM_001354904.2:c.858+9_858+11del	NP_001341833.1:n.858+9_858+11del
NM_001354905.2:c.756+9_756+11del	NP_001341834.1:n.756+9_756+11del
NM_001354906.2:c.84+9_84+11del	NP_001341835.1:n.84+9_84+11del