Canonical Allele Identifier: CA1573484803

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838502_112838504delinsAGT , CM000667.2:g.112838502_112838504delinsAGT	GRCh38
NC_000005.9:g.112174199_112174201delinsAGT , CM000667.1:g.112174199_112174201delinsAGT	GRCh37
NC_000005.8:g.112202098_112202100delinsAGT	NCBI36
NG_008481.4:g.150982_150984delinsAGT , LRG_130:g.150982_150984delinsAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2573_2575delinsAGT	ENSP00000484935.2:n.2573_2575delinsAGT
ENST00000504915.3:c.2962_2964delinsAGT	ENSP00000473355.2:p.Ser988=
ENST00000505350.2:c.*2914_*2916delinsAGT	ENSP00000481752.1:n.*2914_*2916delinsAGT
ENST00000507379.6:c.2854_2856delinsAGT	ENSP00000423224.2:p.Ser952=
ENST00000509732.6:c.2908_2910delinsAGT	ENSP00000426541.2:p.Ser970=
ENST00000512211.7:c.2908_2910delinsAGT	ENSP00000423828.3:p.Ser970=
ENST00000257430.9:c.2908_2910delinsAGT MANE Select	ENSP00000257430.4:p.Ser970=
ENST00000257430.8:c.2908_2910delinsAGT	ENSP00000257430.4:p.Ser970=
ENST00000502371.2:c.1261_1263delinsAGT
ENST00000507379.5:c.2854_2856delinsAGT	ENSP00000423224.1:p.Ser952=
ENST00000508376.6:c.2908_2910delinsAGT	ENSP00000427089.2:p.Ser970=
ENST00000508624.5:c.*2230_*2232delinsAGT	ENSP00000424265.1:n.*2230_*2232delinsAGT
ENST00000512211.6:c.2908_2910delinsAGT	ENSP00000423828.2:p.Ser970=
ENST00000520401.1:c.230+9530_230+9532delinsAGT
NM_000038.5:c.2908_2910delinsAGT	NP_000029.2:p.Ser970=
NM_001127510.2:c.2908_2910delinsAGT	NP_001120982.1:p.Ser970=
NM_001127511.2:c.2854_2856delinsAGT	NP_001120983.2:p.Ser952=
NM_001354895.1:c.2908_2910delinsAGT	NP_001341824.1:p.Ser970=
NM_001354896.1:c.2962_2964delinsAGT	NP_001341825.1:p.Ser988=
NM_001354897.1:c.2938_2940delinsAGT	NP_001341826.1:p.Ser980=
NM_001354898.1:c.2833_2835delinsAGT	NP_001341827.1:p.Ser945=
NM_001354899.1:c.2824_2826delinsAGT	NP_001341828.1:p.Ser942=
NM_001354900.1:c.2785_2787delinsAGT	NP_001341829.1:p.Ser929=
NM_001354901.1:c.2731_2733delinsAGT	NP_001341830.1:p.Ser911=
NM_001354902.1:c.2635_2637delinsAGT	NP_001341831.1:p.Ser879=
NM_001354903.1:c.2605_2607delinsAGT	NP_001341832.1:p.Ser869=
NM_001354904.1:c.2530_2532delinsAGT	NP_001341833.1:p.Ser844=
NM_001354905.1:c.2428_2430delinsAGT	NP_001341834.1:p.Ser810=
NM_001354906.1:c.2059_2061delinsAGT	NP_001341835.1:p.Ser687=
NM_000038.6:c.2908_2910delinsAGT MANE Select	NP_000029.2:p.Ser970=
NM_001127510.3:c.2908_2910delinsAGT	NP_001120982.1:p.Ser970=
NM_001127511.3:c.2854_2856delinsAGT	NP_001120983.2:p.Ser952=
NM_001354895.2:c.2908_2910delinsAGT	NP_001341824.1:p.Ser970=
NM_001354896.2:c.2962_2964delinsAGT	NP_001341825.1:p.Ser988=
NM_001354897.2:c.2938_2940delinsAGT	NP_001341826.1:p.Ser980=
NM_001354898.2:c.2833_2835delinsAGT	NP_001341827.1:p.Ser945=
NM_001354899.2:c.2824_2826delinsAGT	NP_001341828.1:p.Ser942=
NM_001354900.2:c.2785_2787delinsAGT	NP_001341829.1:p.Ser929=
NM_001354901.2:c.2731_2733delinsAGT	NP_001341830.1:p.Ser911=
NM_001354902.2:c.2635_2637delinsAGT	NP_001341831.1:p.Ser879=
NM_001354903.2:c.2605_2607delinsAGT	NP_001341832.1:p.Ser869=
NM_001354904.2:c.2530_2532delinsAGT	NP_001341833.1:p.Ser844=
NM_001354905.2:c.2428_2430delinsAGT	NP_001341834.1:p.Ser810=
NM_001354906.2:c.2059_2061delinsAGT	NP_001341835.1:p.Ser687=