Canonical Allele Identifier: CA1573485762

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838653_112838656delinsAACT , CM000667.2:g.112838653_112838656delinsAACT	GRCh38
NC_000005.9:g.112174350_112174353delinsAACT , CM000667.1:g.112174350_112174353delinsAACT	GRCh37
NC_000005.8:g.112202249_112202252delinsAACT	NCBI36
NG_008481.4:g.151133_151136delinsAACT , LRG_130:g.151133_151136delinsAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2724_2727delinsAACT	ENSP00000484935.2:n.2724_2727delinsAACT
ENST00000504915.3:c.3113_3116delinsAACT	ENSP00000473355.2:p.Glu1038=
ENST00000505350.2:c.*3065_*3068delinsAACT	ENSP00000481752.1:n.*3065_*3068delinsAACT
ENST00000507379.6:c.3005_3008delinsAACT	ENSP00000423224.2:p.Glu1002=
ENST00000509732.6:c.3059_3062delinsAACT	ENSP00000426541.2:p.Glu1020=
ENST00000512211.7:c.3059_3062delinsAACT	ENSP00000423828.3:p.Glu1020=
ENST00000257430.9:c.3059_3062delinsAACT MANE Select	ENSP00000257430.4:p.Glu1020=
ENST00000257430.8:c.3059_3062delinsAACT	ENSP00000257430.4:p.Glu1020=
ENST00000502371.2:c.1412_1415delinsAACT
ENST00000507379.5:c.3005_3008delinsAACT	ENSP00000423224.1:p.Glu1002=
ENST00000508376.6:c.3059_3062delinsAACT	ENSP00000427089.2:p.Glu1020=
ENST00000508624.5:c.*2381_*2384delinsAACT	ENSP00000424265.1:n.*2381_*2384delinsAACT
ENST00000512211.6:c.3059_3062delinsAACT	ENSP00000423828.2:p.Glu1020=
ENST00000520401.1:c.230+9681_230+9684delinsAACT
NM_000038.5:c.3059_3062delinsAACT	NP_000029.2:p.Glu1020=
NM_001127510.2:c.3059_3062delinsAACT	NP_001120982.1:p.Glu1020=
NM_001127511.2:c.3005_3008delinsAACT	NP_001120983.2:p.Glu1002=
NM_001354895.1:c.3059_3062delinsAACT	NP_001341824.1:p.Glu1020=
NM_001354896.1:c.3113_3116delinsAACT	NP_001341825.1:p.Glu1038=
NM_001354897.1:c.3089_3092delinsAACT	NP_001341826.1:p.Glu1030=
NM_001354898.1:c.2984_2987delinsAACT	NP_001341827.1:p.Glu995=
NM_001354899.1:c.2975_2978delinsAACT	NP_001341828.1:p.Glu992=
NM_001354900.1:c.2936_2939delinsAACT	NP_001341829.1:p.Glu979=
NM_001354901.1:c.2882_2885delinsAACT	NP_001341830.1:p.Glu961=
NM_001354902.1:c.2786_2789delinsAACT	NP_001341831.1:p.Glu929=
NM_001354903.1:c.2756_2759delinsAACT	NP_001341832.1:p.Glu919=
NM_001354904.1:c.2681_2684delinsAACT	NP_001341833.1:p.Glu894=
NM_001354905.1:c.2579_2582delinsAACT	NP_001341834.1:p.Glu860=
NM_001354906.1:c.2210_2213delinsAACT	NP_001341835.1:p.Glu737=
NM_000038.6:c.3059_3062delinsAACT MANE Select	NP_000029.2:p.Glu1020=
NM_001127510.3:c.3059_3062delinsAACT	NP_001120982.1:p.Glu1020=
NM_001127511.3:c.3005_3008delinsAACT	NP_001120983.2:p.Glu1002=
NM_001354895.2:c.3059_3062delinsAACT	NP_001341824.1:p.Glu1020=
NM_001354896.2:c.3113_3116delinsAACT	NP_001341825.1:p.Glu1038=
NM_001354897.2:c.3089_3092delinsAACT	NP_001341826.1:p.Glu1030=
NM_001354898.2:c.2984_2987delinsAACT	NP_001341827.1:p.Glu995=
NM_001354899.2:c.2975_2978delinsAACT	NP_001341828.1:p.Glu992=
NM_001354900.2:c.2936_2939delinsAACT	NP_001341829.1:p.Glu979=
NM_001354901.2:c.2882_2885delinsAACT	NP_001341830.1:p.Glu961=
NM_001354902.2:c.2786_2789delinsAACT	NP_001341831.1:p.Glu929=
NM_001354903.2:c.2756_2759delinsAACT	NP_001341832.1:p.Glu919=
NM_001354904.2:c.2681_2684delinsAACT	NP_001341833.1:p.Glu894=
NM_001354905.2:c.2579_2582delinsAACT	NP_001341834.1:p.Glu860=
NM_001354906.2:c.2210_2213delinsAACT	NP_001341835.1:p.Glu737=