Canonical Allele Identifier: CA1573486089

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838707_112838709delinsCTG , CM000667.2:g.112838707_112838709delinsCTG	GRCh38
NC_000005.9:g.112174404_112174406delinsCTG , CM000667.1:g.112174404_112174406delinsCTG	GRCh37
NC_000005.8:g.112202303_112202305delinsCTG	NCBI36
NG_008481.4:g.151187_151189delinsCTG , LRG_130:g.151187_151189delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2778_2780delinsCTG	ENSP00000484935.2:n.2778_2780delinsCTG
ENST00000504915.3:c.3167_3169delinsCTG	ENSP00000473355.2:p.Ser1056=
ENST00000505350.2:c.*3119_*3121delinsCTG	ENSP00000481752.1:n.*3119_*3121delinsCTG
ENST00000507379.6:c.3059_3061delinsCTG	ENSP00000423224.2:p.Ser1020=
ENST00000509732.6:c.3113_3115delinsCTG	ENSP00000426541.2:p.Ser1038=
ENST00000512211.7:c.3113_3115delinsCTG	ENSP00000423828.3:p.Ser1038=
ENST00000257430.9:c.3113_3115delinsCTG MANE Select	ENSP00000257430.4:p.Ser1038=
ENST00000257430.8:c.3113_3115delinsCTG	ENSP00000257430.4:p.Ser1038=
ENST00000502371.2:c.1466_1468delinsCTG
ENST00000507379.5:c.3059_3061delinsCTG	ENSP00000423224.1:p.Ser1020=
ENST00000508376.6:c.3113_3115delinsCTG	ENSP00000427089.2:p.Ser1038=
ENST00000508624.5:c.*2435_*2437delinsCTG	ENSP00000424265.1:n.*2435_*2437delinsCTG
ENST00000512211.6:c.3113_3115delinsCTG	ENSP00000423828.2:p.Ser1038=
ENST00000520401.1:c.230+9735_230+9737delinsCTG
NM_000038.5:c.3113_3115delinsCTG	NP_000029.2:p.Ser1038=
NM_001127510.2:c.3113_3115delinsCTG	NP_001120982.1:p.Ser1038=
NM_001127511.2:c.3059_3061delinsCTG	NP_001120983.2:p.Ser1020=
NM_001354895.1:c.3113_3115delinsCTG	NP_001341824.1:p.Ser1038=
NM_001354896.1:c.3167_3169delinsCTG	NP_001341825.1:p.Ser1056=
NM_001354897.1:c.3143_3145delinsCTG	NP_001341826.1:p.Ser1048=
NM_001354898.1:c.3038_3040delinsCTG	NP_001341827.1:p.Ser1013=
NM_001354899.1:c.3029_3031delinsCTG	NP_001341828.1:p.Ser1010=
NM_001354900.1:c.2990_2992delinsCTG	NP_001341829.1:p.Ser997=
NM_001354901.1:c.2936_2938delinsCTG	NP_001341830.1:p.Ser979=
NM_001354902.1:c.2840_2842delinsCTG	NP_001341831.1:p.Ser947=
NM_001354903.1:c.2810_2812delinsCTG	NP_001341832.1:p.Ser937=
NM_001354904.1:c.2735_2737delinsCTG	NP_001341833.1:p.Ser912=
NM_001354905.1:c.2633_2635delinsCTG	NP_001341834.1:p.Ser878=
NM_001354906.1:c.2264_2266delinsCTG	NP_001341835.1:p.Ser755=
NM_000038.6:c.3113_3115delinsCTG MANE Select	NP_000029.2:p.Ser1038=
NM_001127510.3:c.3113_3115delinsCTG	NP_001120982.1:p.Ser1038=
NM_001127511.3:c.3059_3061delinsCTG	NP_001120983.2:p.Ser1020=
NM_001354895.2:c.3113_3115delinsCTG	NP_001341824.1:p.Ser1038=
NM_001354896.2:c.3167_3169delinsCTG	NP_001341825.1:p.Ser1056=
NM_001354897.2:c.3143_3145delinsCTG	NP_001341826.1:p.Ser1048=
NM_001354898.2:c.3038_3040delinsCTG	NP_001341827.1:p.Ser1013=
NM_001354899.2:c.3029_3031delinsCTG	NP_001341828.1:p.Ser1010=
NM_001354900.2:c.2990_2992delinsCTG	NP_001341829.1:p.Ser997=
NM_001354901.2:c.2936_2938delinsCTG	NP_001341830.1:p.Ser979=
NM_001354902.2:c.2840_2842delinsCTG	NP_001341831.1:p.Ser947=
NM_001354903.2:c.2810_2812delinsCTG	NP_001341832.1:p.Ser937=
NM_001354904.2:c.2735_2737delinsCTG	NP_001341833.1:p.Ser912=
NM_001354905.2:c.2633_2635delinsCTG	NP_001341834.1:p.Ser878=
NM_001354906.2:c.2264_2266delinsCTG	NP_001341835.1:p.Ser755=