Canonical Allele Identifier: CA1573492926

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819257_112819258delinsCT , CM000667.2:g.112819257_112819258delinsCT	GRCh38
NC_000005.9:g.112154954_112154955delinsCT , CM000667.1:g.112154954_112154955delinsCT	GRCh37
NC_000005.8:g.112182853_112182854delinsCT	NCBI36
NG_008481.4:g.131737_131738delinsCT , LRG_130:g.131737_131738delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1225_1226delinsCT	ENSP00000484935.2:p.Leu409=
ENST00000504915.3:c.1225_1226delinsCT	ENSP00000473355.2:p.Leu409=
ENST00000505084.2:n.1281_1282delinsCT
ENST00000505350.2:c.*1231_*1232delinsCT	ENSP00000481752.1:n.*1231_*1232delinsCT
ENST00000507379.6:c.1171_1172delinsCT	ENSP00000423224.2:p.Leu391=
ENST00000509732.6:c.1225_1226delinsCT	ENSP00000426541.2:p.Leu409=
ENST00000512211.7:c.1225_1226delinsCT	ENSP00000423828.3:p.Leu409=
ENST00000257430.9:c.1225_1226delinsCT MANE Select	ENSP00000257430.4:p.Leu409=
ENST00000257430.8:c.1225_1226delinsCT	ENSP00000257430.4:p.Leu409=
ENST00000507379.5:c.1171_1172delinsCT	ENSP00000423224.1:p.Leu391=
ENST00000508376.6:c.1225_1226delinsCT	ENSP00000427089.2:p.Leu409=
ENST00000508624.5:c.*547_*548delinsCT	ENSP00000424265.1:n.*547_*548delinsCT
ENST00000512211.6:c.1225_1226delinsCT	ENSP00000423828.2:p.Leu409=
NM_000038.5:c.1225_1226delinsCT	NP_000029.2:p.Leu409=
NM_001127510.2:c.1225_1226delinsCT	NP_001120982.1:p.Leu409=
NM_001127511.2:c.1171_1172delinsCT	NP_001120983.2:p.Leu391=
NM_001354895.1:c.1225_1226delinsCT	NP_001341824.1:p.Leu409=
NM_001354896.1:c.1225_1226delinsCT	NP_001341825.1:p.Leu409=
NM_001354897.1:c.1255_1256delinsCT	NP_001341826.1:p.Leu419=
NM_001354898.1:c.1150_1151delinsCT	NP_001341827.1:p.Leu384=
NM_001354899.1:c.1141_1142delinsCT	NP_001341828.1:p.Leu381=
NM_001354900.1:c.1048_1049delinsCT	NP_001341829.1:p.Leu350=
NM_001354901.1:c.1048_1049delinsCT	NP_001341830.1:p.Leu350=
NM_001354902.1:c.964-12_964-11delinsCT	NP_001341831.1:n.964-12_964-11delinsCT
NM_001354903.1:c.934-12_934-11delinsCT	NP_001341832.1:n.934-12_934-11delinsCT
NM_001354904.1:c.859-12_859-11delinsCT	NP_001341833.1:n.859-12_859-11delinsCT
NM_001354905.1:c.757-12_757-11delinsCT	NP_001341834.1:n.757-12_757-11delinsCT
NM_001354906.1:c.376_377delinsCT	NP_001341835.1:p.Leu126=
NM_000038.6:c.1225_1226delinsCT MANE Select	NP_000029.2:p.Leu409=
NM_001127510.3:c.1225_1226delinsCT	NP_001120982.1:p.Leu409=
NM_001127511.3:c.1171_1172delinsCT	NP_001120983.2:p.Leu391=
NM_001354895.2:c.1225_1226delinsCT	NP_001341824.1:p.Leu409=
NM_001354896.2:c.1225_1226delinsCT	NP_001341825.1:p.Leu409=
NM_001354897.2:c.1255_1256delinsCT	NP_001341826.1:p.Leu419=
NM_001354898.2:c.1150_1151delinsCT	NP_001341827.1:p.Leu384=
NM_001354899.2:c.1141_1142delinsCT	NP_001341828.1:p.Leu381=
NM_001354900.2:c.1048_1049delinsCT	NP_001341829.1:p.Leu350=
NM_001354901.2:c.1048_1049delinsCT	NP_001341830.1:p.Leu350=
NM_001354902.2:c.964-12_964-11delinsCT	NP_001341831.1:n.964-12_964-11delinsCT
NM_001354903.2:c.934-12_934-11delinsCT	NP_001341832.1:n.934-12_934-11delinsCT
NM_001354904.2:c.859-12_859-11delinsCT	NP_001341833.1:n.859-12_859-11delinsCT
NM_001354905.2:c.757-12_757-11delinsCT	NP_001341834.1:n.757-12_757-11delinsCT
NM_001354906.2:c.376_377delinsCT	NP_001341835.1:p.Leu126=