Canonical Allele Identifier: CA2695204930

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838966dup , CM000667.2:g.112838966dup	GRCh38
NC_000005.9:g.112174663dup , CM000667.1:g.112174663dup	GRCh37
NC_000005.8:g.112202562dup	NCBI36
NG_008481.4:g.151446dup , LRG_130:g.151446dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3037dup	ENSP00000484935.2:n.3037dup
ENST00000504915.3:c.3426dup	ENSP00000473355.2:p.Val1143CysfsTer10
ENST00000505350.2:c.*3378dup	ENSP00000481752.1:n.*3378dup
ENST00000507379.6:c.3318dup	ENSP00000423224.2:p.Val1107CysfsTer10
ENST00000509732.6:c.3372dup	ENSP00000426541.2:p.Val1125CysfsTer10
ENST00000512211.7:c.3372dup	ENSP00000423828.3:p.Val1125CysfsTer10
ENST00000257430.9:c.3372dup MANE Select	ENSP00000257430.4:p.Val1125CysfsTer10
ENST00000257430.8:c.3372dup	ENSP00000257430.4:p.Val1125CysfsTer10
ENST00000502371.2:c.1725dup
ENST00000507379.5:c.3318dup	ENSP00000423224.1:p.Val1107CysfsTer10
ENST00000508376.6:c.3372dup	ENSP00000427089.2:p.Val1125CysfsTer10
ENST00000508624.5:c.*2694dup	ENSP00000424265.1:n.*2694dup
ENST00000512211.6:c.3372dup	ENSP00000423828.2:p.Val1125CysfsTer10
ENST00000520401.1:c.230+9994dup
NM_000038.5:c.3372dup	NP_000029.2:p.Val1125CysfsTer10
NM_001127510.2:c.3372dup	NP_001120982.1:p.Val1125CysfsTer10
NM_001127511.2:c.3318dup	NP_001120983.2:p.Val1107CysfsTer10
NM_001354895.1:c.3372dup	NP_001341824.1:p.Val1125CysfsTer10
NM_001354896.1:c.3426dup	NP_001341825.1:p.Val1143CysfsTer10
NM_001354897.1:c.3402dup	NP_001341826.1:p.Val1135CysfsTer10
NM_001354898.1:c.3297dup	NP_001341827.1:p.Val1100CysfsTer10
NM_001354899.1:c.3288dup	NP_001341828.1:p.Val1097CysfsTer10
NM_001354900.1:c.3249dup	NP_001341829.1:p.Val1084CysfsTer10
NM_001354901.1:c.3195dup	NP_001341830.1:p.Val1066CysfsTer10
NM_001354902.1:c.3099dup	NP_001341831.1:p.Val1034CysfsTer10
NM_001354903.1:c.3069dup	NP_001341832.1:p.Val1024CysfsTer10
NM_001354904.1:c.2994dup	NP_001341833.1:p.Val999CysfsTer10
NM_001354905.1:c.2892dup	NP_001341834.1:p.Val965CysfsTer10
NM_001354906.1:c.2523dup	NP_001341835.1:p.Val842CysfsTer10
NM_000038.6:c.3372dup MANE Select	NP_000029.2:p.Val1125CysfsTer10
NM_001127510.3:c.3372dup	NP_001120982.1:p.Val1125CysfsTer10
NM_001127511.3:c.3318dup	NP_001120983.2:p.Val1107CysfsTer10
NM_001354895.2:c.3372dup	NP_001341824.1:p.Val1125CysfsTer10
NM_001354896.2:c.3426dup	NP_001341825.1:p.Val1143CysfsTer10
NM_001354897.2:c.3402dup	NP_001341826.1:p.Val1135CysfsTer10
NM_001354898.2:c.3297dup	NP_001341827.1:p.Val1100CysfsTer10
NM_001354899.2:c.3288dup	NP_001341828.1:p.Val1097CysfsTer10
NM_001354900.2:c.3249dup	NP_001341829.1:p.Val1084CysfsTer10
NM_001354901.2:c.3195dup	NP_001341830.1:p.Val1066CysfsTer10
NM_001354902.2:c.3099dup	NP_001341831.1:p.Val1034CysfsTer10
NM_001354903.2:c.3069dup	NP_001341832.1:p.Val1024CysfsTer10
NM_001354904.2:c.2994dup	NP_001341833.1:p.Val999CysfsTer10
NM_001354905.2:c.2892dup	NP_001341834.1:p.Val965CysfsTer10
NM_001354906.2:c.2523dup	NP_001341835.1:p.Val842CysfsTer10