Canonical Allele Identifier: CA2767942865

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819197_112819198insCACCCAAC , CM000667.2:g.112819197_112819198insCACCCAAC	GRCh38
NC_000005.9:g.112154894_112154895insCACCCAAC , CM000667.1:g.112154894_112154895insCACCCAAC	GRCh37
NC_000005.8:g.112182793_112182794insCACCCAAC	NCBI36
NG_008481.4:g.131677_131678insCACCCAAC , LRG_130:g.131677_131678insCACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1165_1166insCACCCAAC	ENSP00000484935.2:p.Asn389ThrfsTer?
ENST00000504915.3:c.1165_1166insCACCCAAC	ENSP00000473355.2:p.Asn389ThrfsTer?
ENST00000505084.2:n.1221_1222insCACCCAAC
ENST00000505350.2:c.*1171_*1172insCACCCAAC	ENSP00000481752.1:n.*1171_*1172insCACCCAAC
ENST00000507379.6:c.1111_1112insCACCCAAC	ENSP00000423224.2:p.Asn371ThrfsTer?
ENST00000509732.6:c.1165_1166insCACCCAAC	ENSP00000426541.2:p.Asn389ThrfsTer?
ENST00000512211.7:c.1165_1166insCACCCAAC	ENSP00000423828.3:p.Asn389ThrfsTer?
ENST00000257430.9:c.1165_1166insCACCCAAC MANE Select	ENSP00000257430.4:p.Asn389ThrfsTer?
ENST00000257430.8:c.1165_1166insCACCCAAC	ENSP00000257430.4:p.Asn389ThrfsTer?
ENST00000507379.5:c.1111_1112insCACCCAAC	ENSP00000423224.1:p.Asn371ThrfsTer?
ENST00000508376.6:c.1165_1166insCACCCAAC	ENSP00000427089.2:p.Asn389ThrfsTer?
ENST00000508624.5:c.*487_*488insCACCCAAC	ENSP00000424265.1:n.*487_*488insCACCCAAC
ENST00000512211.6:c.1165_1166insCACCCAAC	ENSP00000423828.2:p.Asn389ThrfsTer?
NM_000038.5:c.1165_1166insCACCCAAC	NP_000029.2:p.Asn389ThrfsTer?
NM_001127510.2:c.1165_1166insCACCCAAC	NP_001120982.1:p.Asn389ThrfsTer?
NM_001127511.2:c.1111_1112insCACCCAAC	NP_001120983.2:p.Asn371ThrfsTer?
NM_001354895.1:c.1165_1166insCACCCAAC	NP_001341824.1:p.Asn389ThrfsTer?
NM_001354896.1:c.1165_1166insCACCCAAC	NP_001341825.1:p.Asn389ThrfsTer?
NM_001354897.1:c.1195_1196insCACCCAAC	NP_001341826.1:p.Asn399ThrfsTer?
NM_001354898.1:c.1090_1091insCACCCAAC	NP_001341827.1:p.Asn364ThrfsTer?
NM_001354899.1:c.1081_1082insCACCCAAC	NP_001341828.1:p.Asn361ThrfsTer?
NM_001354900.1:c.988_989insCACCCAAC	NP_001341829.1:p.Asn330ThrfsTer?
NM_001354901.1:c.988_989insCACCCAAC	NP_001341830.1:p.Asn330ThrfsTer?
NM_001354902.1:c.964-72_964-71insCACCCAAC	NP_001341831.1:n.964-72_964-71insCACCCAAC
NM_001354903.1:c.934-72_934-71insCACCCAAC	NP_001341832.1:n.934-72_934-71insCACCCAAC
NM_001354904.1:c.859-72_859-71insCACCCAAC	NP_001341833.1:n.859-72_859-71insCACCCAAC
NM_001354905.1:c.757-72_757-71insCACCCAAC	NP_001341834.1:n.757-72_757-71insCACCCAAC
NM_001354906.1:c.316_317insCACCCAAC	NP_001341835.1:p.Asn106ThrfsTer?
NM_000038.6:c.1165_1166insCACCCAAC MANE Select	NP_000029.2:p.Asn389ThrfsTer?
NM_001127510.3:c.1165_1166insCACCCAAC	NP_001120982.1:p.Asn389ThrfsTer?
NM_001127511.3:c.1111_1112insCACCCAAC	NP_001120983.2:p.Asn371ThrfsTer?
NM_001354895.2:c.1165_1166insCACCCAAC	NP_001341824.1:p.Asn389ThrfsTer?
NM_001354896.2:c.1165_1166insCACCCAAC	NP_001341825.1:p.Asn389ThrfsTer?
NM_001354897.2:c.1195_1196insCACCCAAC	NP_001341826.1:p.Asn399ThrfsTer?
NM_001354898.2:c.1090_1091insCACCCAAC	NP_001341827.1:p.Asn364ThrfsTer?
NM_001354899.2:c.1081_1082insCACCCAAC	NP_001341828.1:p.Asn361ThrfsTer?
NM_001354900.2:c.988_989insCACCCAAC	NP_001341829.1:p.Asn330ThrfsTer?
NM_001354901.2:c.988_989insCACCCAAC	NP_001341830.1:p.Asn330ThrfsTer?
NM_001354902.2:c.964-72_964-71insCACCCAAC	NP_001341831.1:n.964-72_964-71insCACCCAAC
NM_001354903.2:c.934-72_934-71insCACCCAAC	NP_001341832.1:n.934-72_934-71insCACCCAAC
NM_001354904.2:c.859-72_859-71insCACCCAAC	NP_001341833.1:n.859-72_859-71insCACCCAAC
NM_001354905.2:c.757-72_757-71insCACCCAAC	NP_001341834.1:n.757-72_757-71insCACCCAAC
NM_001354906.2:c.316_317insCACCCAAC	NP_001341835.1:p.Asn106ThrfsTer?