Canonical Allele Identifier: CA1573484700

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815531_112815532delinsGT , CM000667.2:g.112815531_112815532delinsGT	GRCh38
NC_000005.9:g.112151228_112151229delinsGT , CM000667.1:g.112151228_112151229delinsGT	GRCh37
NC_000005.8:g.112179127_112179128delinsGT	NCBI36
NG_008481.4:g.128011_128012delinsGT , LRG_130:g.128011_128012delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.871_872delinsGT	ENSP00000484935.2:p.Val291=
ENST00000504915.3:c.871_872delinsGT	ENSP00000473355.2:p.Val291=
ENST00000505084.2:n.927_928delinsGT
ENST00000505350.2:c.*877_*878delinsGT	ENSP00000481752.1:n.*877_*878delinsGT
ENST00000507379.6:c.817_818delinsGT	ENSP00000423224.2:p.Val273=
ENST00000509732.6:c.871_872delinsGT	ENSP00000426541.2:p.Val291=
ENST00000512211.7:c.871_872delinsGT	ENSP00000423828.3:p.Val291=
ENST00000257430.9:c.871_872delinsGT MANE Select	ENSP00000257430.4:p.Val291=
ENST00000257430.8:c.871_872delinsGT	ENSP00000257430.4:p.Val291=
ENST00000507379.5:c.817_818delinsGT	ENSP00000423224.1:p.Val273=
ENST00000508376.6:c.871_872delinsGT	ENSP00000427089.2:p.Val291=
ENST00000508624.5:c.*193_*194delinsGT	ENSP00000424265.1:n.*193_*194delinsGT
ENST00000512211.6:c.871_872delinsGT	ENSP00000423828.2:p.Val291=
NM_000038.5:c.871_872delinsGT	NP_000029.2:p.Val291=
NM_001127510.2:c.871_872delinsGT	NP_001120982.1:p.Val291=
NM_001127511.2:c.817_818delinsGT	NP_001120983.2:p.Val273=
NM_001354895.1:c.871_872delinsGT	NP_001341824.1:p.Val291=
NM_001354896.1:c.871_872delinsGT	NP_001341825.1:p.Val291=
NM_001354897.1:c.901_902delinsGT	NP_001341826.1:p.Val301=
NM_001354898.1:c.796_797delinsGT	NP_001341827.1:p.Val266=
NM_001354899.1:c.787_788delinsGT	NP_001341828.1:p.Val263=
NM_001354900.1:c.694_695delinsGT	NP_001341829.1:p.Val232=
NM_001354901.1:c.694_695delinsGT	NP_001341830.1:p.Val232=
NM_001354902.1:c.901_902delinsGT	NP_001341831.1:p.Val301=
NM_001354903.1:c.871_872delinsGT	NP_001341832.1:p.Val291=
NM_001354904.1:c.796_797delinsGT	NP_001341833.1:p.Val266=
NM_001354905.1:c.694_695delinsGT	NP_001341834.1:p.Val232=
NM_001354906.1:c.22_23delinsGT	NP_001341835.1:p.Val8=
NM_000038.6:c.871_872delinsGT MANE Select	NP_000029.2:p.Val291=
NM_001127510.3:c.871_872delinsGT	NP_001120982.1:p.Val291=
NM_001127511.3:c.817_818delinsGT	NP_001120983.2:p.Val273=
NM_001354895.2:c.871_872delinsGT	NP_001341824.1:p.Val291=
NM_001354896.2:c.871_872delinsGT	NP_001341825.1:p.Val291=
NM_001354897.2:c.901_902delinsGT	NP_001341826.1:p.Val301=
NM_001354898.2:c.796_797delinsGT	NP_001341827.1:p.Val266=
NM_001354899.2:c.787_788delinsGT	NP_001341828.1:p.Val263=
NM_001354900.2:c.694_695delinsGT	NP_001341829.1:p.Val232=
NM_001354901.2:c.694_695delinsGT	NP_001341830.1:p.Val232=
NM_001354902.2:c.901_902delinsGT	NP_001341831.1:p.Val301=
NM_001354903.2:c.871_872delinsGT	NP_001341832.1:p.Val291=
NM_001354904.2:c.796_797delinsGT	NP_001341833.1:p.Val266=
NM_001354905.2:c.694_695delinsGT	NP_001341834.1:p.Val232=
NM_001354906.2:c.22_23delinsGT	NP_001341835.1:p.Val8=