Canonical Allele Identifier: CA1573492977

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819271_112819272delinsAC , CM000667.2:g.112819271_112819272delinsAC	GRCh38
NC_000005.9:g.112154968_112154969delinsAC , CM000667.1:g.112154968_112154969delinsAC	GRCh37
NC_000005.8:g.112182867_112182868delinsAC	NCBI36
NG_008481.4:g.131751_131752delinsAC , LRG_130:g.131751_131752delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1239_1240delinsAC	ENSP00000484935.2:p.Ile413=
ENST00000504915.3:c.1239_1240delinsAC	ENSP00000473355.2:p.Ile413=
ENST00000505084.2:n.1295_1296delinsAC
ENST00000505350.2:c.*1245_*1246delinsAC	ENSP00000481752.1:n.*1245_*1246delinsAC
ENST00000507379.6:c.1185_1186delinsAC	ENSP00000423224.2:p.Ile395=
ENST00000509732.6:c.1239_1240delinsAC	ENSP00000426541.2:p.Ile413=
ENST00000512211.7:c.1239_1240delinsAC	ENSP00000423828.3:p.Ile413=
ENST00000257430.9:c.1239_1240delinsAC MANE Select	ENSP00000257430.4:p.Ile413=
ENST00000257430.8:c.1239_1240delinsAC	ENSP00000257430.4:p.Ile413=
ENST00000507379.5:c.1185_1186delinsAC	ENSP00000423224.1:p.Ile395=
ENST00000508376.6:c.1239_1240delinsAC	ENSP00000427089.2:p.Ile413=
ENST00000508624.5:c.*561_*562delinsAC	ENSP00000424265.1:n.*561_*562delinsAC
ENST00000512211.6:c.1239_1240delinsAC	ENSP00000423828.2:p.Ile413=
NM_000038.5:c.1239_1240delinsAC	NP_000029.2:p.Ile413=
NM_001127510.2:c.1239_1240delinsAC	NP_001120982.1:p.Ile413=
NM_001127511.2:c.1185_1186delinsAC	NP_001120983.2:p.Ile395=
NM_001354895.1:c.1239_1240delinsAC	NP_001341824.1:p.Ile413=
NM_001354896.1:c.1239_1240delinsAC	NP_001341825.1:p.Ile413=
NM_001354897.1:c.1269_1270delinsAC	NP_001341826.1:p.Ile423=
NM_001354898.1:c.1164_1165delinsAC	NP_001341827.1:p.Ile388=
NM_001354899.1:c.1155_1156delinsAC	NP_001341828.1:p.Ile385=
NM_001354900.1:c.1062_1063delinsAC	NP_001341829.1:p.Ile354=
NM_001354901.1:c.1062_1063delinsAC	NP_001341830.1:p.Ile354=
NM_001354902.1:c.966_967delinsAC	NP_001341831.1:p.Ile322=
NM_001354903.1:c.936_937delinsAC	NP_001341832.1:p.Ile312=
NM_001354904.1:c.861_862delinsAC	NP_001341833.1:p.Ile287=
NM_001354905.1:c.759_760delinsAC	NP_001341834.1:p.Ile253=
NM_001354906.1:c.390_391delinsAC	NP_001341835.1:p.Ile130=
NM_000038.6:c.1239_1240delinsAC MANE Select	NP_000029.2:p.Ile413=
NM_001127510.3:c.1239_1240delinsAC	NP_001120982.1:p.Ile413=
NM_001127511.3:c.1185_1186delinsAC	NP_001120983.2:p.Ile395=
NM_001354895.2:c.1239_1240delinsAC	NP_001341824.1:p.Ile413=
NM_001354896.2:c.1239_1240delinsAC	NP_001341825.1:p.Ile413=
NM_001354897.2:c.1269_1270delinsAC	NP_001341826.1:p.Ile423=
NM_001354898.2:c.1164_1165delinsAC	NP_001341827.1:p.Ile388=
NM_001354899.2:c.1155_1156delinsAC	NP_001341828.1:p.Ile385=
NM_001354900.2:c.1062_1063delinsAC	NP_001341829.1:p.Ile354=
NM_001354901.2:c.1062_1063delinsAC	NP_001341830.1:p.Ile354=
NM_001354902.2:c.966_967delinsAC	NP_001341831.1:p.Ile322=
NM_001354903.2:c.936_937delinsAC	NP_001341832.1:p.Ile312=
NM_001354904.2:c.861_862delinsAC	NP_001341833.1:p.Ile287=
NM_001354905.2:c.759_760delinsAC	NP_001341834.1:p.Ile253=
NM_001354906.2:c.390_391delinsAC	NP_001341835.1:p.Ile130=