Canonical Allele Identifier: CA445963184

Gene: APC

Linked Data

• COSMIC: COSM18969
• MyVariant Identifiers: chr5:g.112174407_112174408insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838710dup , CM000667.2:g.112838710dup	GRCh38
NC_000005.9:g.112174407dup , CM000667.1:g.112174407dup	GRCh37
NC_000005.8:g.112202306dup	NCBI36
NG_008481.4:g.151190dup , LRG_130:g.151190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2781dup	ENSP00000484935.2:n.2781dup
ENST00000504915.3:c.3170dup	ENSP00000473355.2:p.Arg1058LysfsTer8
ENST00000505350.2:c.*3122dup	ENSP00000481752.1:n.*3122dup
ENST00000507379.6:c.3062dup	ENSP00000423224.2:p.Arg1022LysfsTer8
ENST00000509732.6:c.3116dup	ENSP00000426541.2:p.Arg1040LysfsTer8
ENST00000512211.7:c.3116dup	ENSP00000423828.3:p.Arg1040LysfsTer8
ENST00000257430.9:c.3116dup MANE Select	ENSP00000257430.4:p.Arg1040LysfsTer8
ENST00000257430.8:c.3116dup	ENSP00000257430.4:p.Arg1040LysfsTer8
ENST00000502371.2:c.1469dup
ENST00000507379.5:c.3062dup	ENSP00000423224.1:p.Arg1022LysfsTer8
ENST00000508376.6:c.3116dup	ENSP00000427089.2:p.Arg1040LysfsTer8
ENST00000508624.5:c.*2438dup	ENSP00000424265.1:n.*2438dup
ENST00000512211.6:c.3116dup	ENSP00000423828.2:p.Arg1040LysfsTer8
ENST00000520401.1:c.230+9738dup
NM_000038.5:c.3116dup	NP_000029.2:p.Arg1040LysfsTer8
NM_001127510.2:c.3116dup	NP_001120982.1:p.Arg1040LysfsTer8
NM_001127511.2:c.3062dup	NP_001120983.2:p.Arg1022LysfsTer8
NM_001354895.1:c.3116dup	NP_001341824.1:p.Arg1040LysfsTer8
NM_001354896.1:c.3170dup	NP_001341825.1:p.Arg1058LysfsTer8
NM_001354897.1:c.3146dup	NP_001341826.1:p.Arg1050LysfsTer8
NM_001354898.1:c.3041dup	NP_001341827.1:p.Arg1015LysfsTer8
NM_001354899.1:c.3032dup	NP_001341828.1:p.Arg1012LysfsTer8
NM_001354900.1:c.2993dup	NP_001341829.1:p.Arg999LysfsTer8
NM_001354901.1:c.2939dup	NP_001341830.1:p.Arg981LysfsTer8
NM_001354902.1:c.2843dup	NP_001341831.1:p.Arg949LysfsTer8
NM_001354903.1:c.2813dup	NP_001341832.1:p.Arg939LysfsTer8
NM_001354904.1:c.2738dup	NP_001341833.1:p.Arg914LysfsTer8
NM_001354905.1:c.2636dup	NP_001341834.1:p.Arg880LysfsTer8
NM_001354906.1:c.2267dup	NP_001341835.1:p.Arg757LysfsTer8
NM_000038.6:c.3116dup MANE Select	NP_000029.2:p.Arg1040LysfsTer8
NM_001127510.3:c.3116dup	NP_001120982.1:p.Arg1040LysfsTer8
NM_001127511.3:c.3062dup	NP_001120983.2:p.Arg1022LysfsTer8
NM_001354895.2:c.3116dup	NP_001341824.1:p.Arg1040LysfsTer8
NM_001354896.2:c.3170dup	NP_001341825.1:p.Arg1058LysfsTer8
NM_001354897.2:c.3146dup	NP_001341826.1:p.Arg1050LysfsTer8
NM_001354898.2:c.3041dup	NP_001341827.1:p.Arg1015LysfsTer8
NM_001354899.2:c.3032dup	NP_001341828.1:p.Arg1012LysfsTer8
NM_001354900.2:c.2993dup	NP_001341829.1:p.Arg999LysfsTer8
NM_001354901.2:c.2939dup	NP_001341830.1:p.Arg981LysfsTer8
NM_001354902.2:c.2843dup	NP_001341831.1:p.Arg949LysfsTer8
NM_001354903.2:c.2813dup	NP_001341832.1:p.Arg939LysfsTer8
NM_001354904.2:c.2738dup	NP_001341833.1:p.Arg914LysfsTer8
NM_001354905.2:c.2636dup	NP_001341834.1:p.Arg880LysfsTer8
NM_001354906.2:c.2267dup	NP_001341835.1:p.Arg757LysfsTer8