Canonical Allele Identifier: CA1573487665

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838928_112838933delinsACAAAT , CM000667.2:g.112838928_112838933delinsACAAAT	GRCh38
NC_000005.9:g.112174625_112174630delinsACAAAT , CM000667.1:g.112174625_112174630delinsACAAAT	GRCh37
NC_000005.8:g.112202524_112202529delinsACAAAT	NCBI36
NG_008481.4:g.151408_151413delinsACAAAT , LRG_130:g.151408_151413delinsACAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2999_3004delinsACAAAT	ENSP00000484935.2:n.2999_3004delinsACAAAT
ENST00000504915.3:c.3388_3393delinsACAAAT	ENSP00000473355.2:p.Thr1130=
ENST00000505350.2:c.*3340_*3345delinsACAAAT	ENSP00000481752.1:n.*3340_*3345delinsACAAAT
ENST00000507379.6:c.3280_3285delinsACAAAT	ENSP00000423224.2:p.Thr1094=
ENST00000509732.6:c.3334_3339delinsACAAAT	ENSP00000426541.2:p.Thr1112=
ENST00000512211.7:c.3334_3339delinsACAAAT	ENSP00000423828.3:p.Thr1112=
ENST00000257430.9:c.3334_3339delinsACAAAT MANE Select	ENSP00000257430.4:p.Thr1112=
ENST00000257430.8:c.3334_3339delinsACAAAT	ENSP00000257430.4:p.Thr1112=
ENST00000502371.2:c.1687_1692delinsACAAAT
ENST00000507379.5:c.3280_3285delinsACAAAT	ENSP00000423224.1:p.Thr1094=
ENST00000508376.6:c.3334_3339delinsACAAAT	ENSP00000427089.2:p.Thr1112=
ENST00000508624.5:c.*2656_*2661delinsACAAAT	ENSP00000424265.1:n.*2656_*2661delinsACAAAT
ENST00000512211.6:c.3334_3339delinsACAAAT	ENSP00000423828.2:p.Thr1112=
ENST00000520401.1:c.230+9956_230+9961delinsACAAAT
NM_000038.5:c.3334_3339delinsACAAAT	NP_000029.2:p.Thr1112=
NM_001127510.2:c.3334_3339delinsACAAAT	NP_001120982.1:p.Thr1112=
NM_001127511.2:c.3280_3285delinsACAAAT	NP_001120983.2:p.Thr1094=
NM_001354895.1:c.3334_3339delinsACAAAT	NP_001341824.1:p.Thr1112=
NM_001354896.1:c.3388_3393delinsACAAAT	NP_001341825.1:p.Thr1130=
NM_001354897.1:c.3364_3369delinsACAAAT	NP_001341826.1:p.Thr1122=
NM_001354898.1:c.3259_3264delinsACAAAT	NP_001341827.1:p.Thr1087=
NM_001354899.1:c.3250_3255delinsACAAAT	NP_001341828.1:p.Thr1084=
NM_001354900.1:c.3211_3216delinsACAAAT	NP_001341829.1:p.Thr1071=
NM_001354901.1:c.3157_3162delinsACAAAT	NP_001341830.1:p.Thr1053=
NM_001354902.1:c.3061_3066delinsACAAAT	NP_001341831.1:p.Thr1021=
NM_001354903.1:c.3031_3036delinsACAAAT	NP_001341832.1:p.Thr1011=
NM_001354904.1:c.2956_2961delinsACAAAT	NP_001341833.1:p.Thr986=
NM_001354905.1:c.2854_2859delinsACAAAT	NP_001341834.1:p.Thr952=
NM_001354906.1:c.2485_2490delinsACAAAT	NP_001341835.1:p.Thr829=
NM_000038.6:c.3334_3339delinsACAAAT MANE Select	NP_000029.2:p.Thr1112=
NM_001127510.3:c.3334_3339delinsACAAAT	NP_001120982.1:p.Thr1112=
NM_001127511.3:c.3280_3285delinsACAAAT	NP_001120983.2:p.Thr1094=
NM_001354895.2:c.3334_3339delinsACAAAT	NP_001341824.1:p.Thr1112=
NM_001354896.2:c.3388_3393delinsACAAAT	NP_001341825.1:p.Thr1130=
NM_001354897.2:c.3364_3369delinsACAAAT	NP_001341826.1:p.Thr1122=
NM_001354898.2:c.3259_3264delinsACAAAT	NP_001341827.1:p.Thr1087=
NM_001354899.2:c.3250_3255delinsACAAAT	NP_001341828.1:p.Thr1084=
NM_001354900.2:c.3211_3216delinsACAAAT	NP_001341829.1:p.Thr1071=
NM_001354901.2:c.3157_3162delinsACAAAT	NP_001341830.1:p.Thr1053=
NM_001354902.2:c.3061_3066delinsACAAAT	NP_001341831.1:p.Thr1021=
NM_001354903.2:c.3031_3036delinsACAAAT	NP_001341832.1:p.Thr1011=
NM_001354904.2:c.2956_2961delinsACAAAT	NP_001341833.1:p.Thr986=
NM_001354905.2:c.2854_2859delinsACAAAT	NP_001341834.1:p.Thr952=
NM_001354906.2:c.2485_2490delinsACAAAT	NP_001341835.1:p.Thr829=