Canonical Allele Identifier: CA1573491970

Gene: APC

Linked Data

• dbSNP Id: rs1759239267

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112788622_112788623del , CM000667.2:g.112788622_112788623del	GRCh38
NC_000005.9:g.112124319_112124320del , CM000667.1:g.112124319_112124320del	GRCh37
NC_000005.8:g.112152218_112152219del	NCBI36
NG_008481.4:g.101102_101103del , LRG_130:g.101102_101103del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.646-3824_646-3823del	ENSP00000484935.2:n.646-3824_646-3823del
ENST00000504915.3:c.646-3824_646-3823del	ENSP00000473355.2:n.646-3824_646-3823del
ENST00000505084.2:n.702-3824_702-3823del
ENST00000505350.2:c.*652-3824_*652-3823del	ENSP00000481752.1:n.*652-3824_*652-3823de...
ENST00000507379.6:c.675+7719_675+7720del	ENSP00000423224.2:n.675+7719_675+7720del
ENST00000509732.6:c.646-3824_646-3823del	ENSP00000426541.2:n.646-3824_646-3823del
ENST00000512211.7:c.646-3824_646-3823del	ENSP00000423828.3:n.646-3824_646-3823del
ENST00000257430.9:c.646-3824_646-3823del MANE Select	ENSP00000257430.4:n.646-3824_646-3823del
ENST00000257430.8:c.646-3824_646-3823del	ENSP00000257430.4:n.646-3824_646-3823del
ENST00000507379.5:c.675+7719_675+7720del	ENSP00000423224.1:n.675+7719_675+7720del
ENST00000508376.6:c.646-3824_646-3823del	ENSP00000427089.2:n.646-3824_646-3823del
ENST00000508624.5:c.646-3824_646-3823del	ENSP00000424265.1:n.646-3824_646-3823del
ENST00000512211.6:c.646-3824_646-3823del	ENSP00000423828.2:n.646-3824_646-3823del
NM_000038.5:c.646-3824_646-3823del	NP_000029.2:n.646-3824_646-3823del
NM_001127510.2:c.646-3824_646-3823del	NP_001120982.1:n.646-3824_646-3823del
NM_001127511.2:c.675+7719_675+7720del	NP_001120983.2:n.675+7719_675+7720del
NM_001354895.1:c.646-3824_646-3823del	NP_001341824.1:n.646-3824_646-3823del
NM_001354896.1:c.646-3824_646-3823del	NP_001341825.1:n.646-3824_646-3823del
NM_001354897.1:c.676-3824_676-3823del	NP_001341826.1:n.676-3824_676-3823del
NM_001354898.1:c.571-3824_571-3823del	NP_001341827.1:n.571-3824_571-3823del
NM_001354899.1:c.645+7719_645+7720del	NP_001341828.1:n.645+7719_645+7720del
NM_001354900.1:c.469-3824_469-3823del	NP_001341829.1:n.469-3824_469-3823del
NM_001354901.1:c.469-3824_469-3823del	NP_001341830.1:n.469-3824_469-3823del
NM_001354902.1:c.676-3824_676-3823del	NP_001341831.1:n.676-3824_676-3823del
NM_001354903.1:c.646-3824_646-3823del	NP_001341832.1:n.646-3824_646-3823del
NM_001354904.1:c.571-3824_571-3823del	NP_001341833.1:n.571-3824_571-3823del
NM_001354905.1:c.469-3824_469-3823del	NP_001341834.1:n.469-3824_469-3823del
NM_001354906.1:c.-390-3824_-390-3823del	NP_001341835.1:n.-390-3824_-390-3823del
NM_000038.6:c.646-3824_646-3823del MANE Select	NP_000029.2:n.646-3824_646-3823del
NM_001127510.3:c.646-3824_646-3823del	NP_001120982.1:n.646-3824_646-3823del
NM_001127511.3:c.675+7719_675+7720del	NP_001120983.2:n.675+7719_675+7720del
NM_001354895.2:c.646-3824_646-3823del	NP_001341824.1:n.646-3824_646-3823del
NM_001354896.2:c.646-3824_646-3823del	NP_001341825.1:n.646-3824_646-3823del
NM_001354897.2:c.676-3824_676-3823del	NP_001341826.1:n.676-3824_676-3823del
NM_001354898.2:c.571-3824_571-3823del	NP_001341827.1:n.571-3824_571-3823del
NM_001354899.2:c.645+7719_645+7720del	NP_001341828.1:n.645+7719_645+7720del
NM_001354900.2:c.469-3824_469-3823del	NP_001341829.1:n.469-3824_469-3823del
NM_001354901.2:c.469-3824_469-3823del	NP_001341830.1:n.469-3824_469-3823del
NM_001354902.2:c.676-3824_676-3823del	NP_001341831.1:n.676-3824_676-3823del
NM_001354903.2:c.646-3824_646-3823del	NP_001341832.1:n.646-3824_646-3823del
NM_001354904.2:c.571-3824_571-3823del	NP_001341833.1:n.571-3824_571-3823del
NM_001354905.2:c.469-3824_469-3823del	NP_001341834.1:n.469-3824_469-3823del
NM_001354906.2:c.-390-3824_-390-3823del	NP_001341835.1:n.-390-3824_-390-3823del