Canonical Allele Identifier: CA1573492997

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819272_112819278delinsCGCGCTT , CM000667.2:g.112819272_112819278delinsCGCGCTT	GRCh38
NC_000005.9:g.112154969_112154975delinsCGCGCTT , CM000667.1:g.112154969_112154975delinsCGCGCTT	GRCh37
NC_000005.8:g.112182868_112182874delinsCGCGCTT	NCBI36
NG_008481.4:g.131752_131758delinsCGCGCTT , LRG_130:g.131752_131758delinsCGCGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1240_1246delinsCGCGCTT	ENSP00000484935.2:p.Arg414=
ENST00000504915.3:c.1240_1246delinsCGCGCTT	ENSP00000473355.2:p.Arg414=
ENST00000505084.2:n.1296_1302delinsCGCGCTT
ENST00000505350.2:c.*1246_*1252delinsCGCGCTT	ENSP00000481752.1:n.*1246_*1252delinsCGCGCTT
ENST00000507379.6:c.1186_1192delinsCGCGCTT	ENSP00000423224.2:p.Arg396=
ENST00000509732.6:c.1240_1246delinsCGCGCTT	ENSP00000426541.2:p.Arg414=
ENST00000512211.7:c.1240_1246delinsCGCGCTT	ENSP00000423828.3:p.Arg414=
ENST00000257430.9:c.1240_1246delinsCGCGCTT MANE Select	ENSP00000257430.4:p.Arg414=
ENST00000257430.8:c.1240_1246delinsCGCGCTT	ENSP00000257430.4:p.Arg414=
ENST00000507379.5:c.1186_1192delinsCGCGCTT	ENSP00000423224.1:p.Arg396=
ENST00000508376.6:c.1240_1246delinsCGCGCTT	ENSP00000427089.2:p.Arg414=
ENST00000508624.5:c.*562_*568delinsCGCGCTT	ENSP00000424265.1:n.*562_*568delinsCGCGCTT
ENST00000512211.6:c.1240_1246delinsCGCGCTT	ENSP00000423828.2:p.Arg414=
NM_000038.5:c.1240_1246delinsCGCGCTT	NP_000029.2:p.Arg414=
NM_001127510.2:c.1240_1246delinsCGCGCTT	NP_001120982.1:p.Arg414=
NM_001127511.2:c.1186_1192delinsCGCGCTT	NP_001120983.2:p.Arg396=
NM_001354895.1:c.1240_1246delinsCGCGCTT	NP_001341824.1:p.Arg414=
NM_001354896.1:c.1240_1246delinsCGCGCTT	NP_001341825.1:p.Arg414=
NM_001354897.1:c.1270_1276delinsCGCGCTT	NP_001341826.1:p.Arg424=
NM_001354898.1:c.1165_1171delinsCGCGCTT	NP_001341827.1:p.Arg389=
NM_001354899.1:c.1156_1162delinsCGCGCTT	NP_001341828.1:p.Arg386=
NM_001354900.1:c.1063_1069delinsCGCGCTT	NP_001341829.1:p.Arg355=
NM_001354901.1:c.1063_1069delinsCGCGCTT	NP_001341830.1:p.Arg355=
NM_001354902.1:c.967_973delinsCGCGCTT	NP_001341831.1:p.Arg323=
NM_001354903.1:c.937_943delinsCGCGCTT	NP_001341832.1:p.Arg313=
NM_001354904.1:c.862_868delinsCGCGCTT	NP_001341833.1:p.Arg288=
NM_001354905.1:c.760_766delinsCGCGCTT	NP_001341834.1:p.Arg254=
NM_001354906.1:c.391_397delinsCGCGCTT	NP_001341835.1:p.Arg131=
NM_000038.6:c.1240_1246delinsCGCGCTT MANE Select	NP_000029.2:p.Arg414=
NM_001127510.3:c.1240_1246delinsCGCGCTT	NP_001120982.1:p.Arg414=
NM_001127511.3:c.1186_1192delinsCGCGCTT	NP_001120983.2:p.Arg396=
NM_001354895.2:c.1240_1246delinsCGCGCTT	NP_001341824.1:p.Arg414=
NM_001354896.2:c.1240_1246delinsCGCGCTT	NP_001341825.1:p.Arg414=
NM_001354897.2:c.1270_1276delinsCGCGCTT	NP_001341826.1:p.Arg424=
NM_001354898.2:c.1165_1171delinsCGCGCTT	NP_001341827.1:p.Arg389=
NM_001354899.2:c.1156_1162delinsCGCGCTT	NP_001341828.1:p.Arg386=
NM_001354900.2:c.1063_1069delinsCGCGCTT	NP_001341829.1:p.Arg355=
NM_001354901.2:c.1063_1069delinsCGCGCTT	NP_001341830.1:p.Arg355=
NM_001354902.2:c.967_973delinsCGCGCTT	NP_001341831.1:p.Arg323=
NM_001354903.2:c.937_943delinsCGCGCTT	NP_001341832.1:p.Arg313=
NM_001354904.2:c.862_868delinsCGCGCTT	NP_001341833.1:p.Arg288=
NM_001354905.2:c.760_766delinsCGCGCTT	NP_001341834.1:p.Arg254=
NM_001354906.2:c.391_397delinsCGCGCTT	NP_001341835.1:p.Arg131=