Canonical Allele Identifier: CA008388

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839062_112839064del , CM000667.2:g.112839062_112839064del	GRCh38
NC_000005.9:g.112174759_112174761del , CM000667.1:g.112174759_112174761del	GRCh37
NC_000005.8:g.112202658_112202660del	NCBI36
NG_008481.4:g.151542_151544del , LRG_130:g.151542_151544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3133_3135del	ENSP00000484935.2:n.3133_3135del
ENST00000504915.3:c.3522_3524del	ENSP00000473355.2:p.Glu1175del
ENST00000505350.2:c.*3474_*3476del	ENSP00000481752.1:n.*3474_*3476del
ENST00000507379.6:c.3414_3416del	ENSP00000423224.2:p.Glu1139del
ENST00000509732.6:c.3468_3470del	ENSP00000426541.2:p.Glu1157del
ENST00000512211.7:c.3468_3470del	ENSP00000423828.3:p.Glu1157del
ENST00000257430.9:c.3468_3470del MANE Select	ENSP00000257430.4:p.Glu1157del
ENST00000257430.8:c.3468_3470del	ENSP00000257430.4:p.Glu1157del
ENST00000502371.2:c.1821_1823del
ENST00000508376.6:c.3468_3470del	ENSP00000427089.2:p.Glu1157del
ENST00000508624.5:c.*2790_*2792del	ENSP00000424265.1:n.*2790_*2792del
ENST00000512211.6:c.3468_3470del	ENSP00000423828.2:p.Glu1157del
ENST00000520401.1:c.230+10090_230+10092del
NM_000038.5:c.3468_3470del	NP_000029.2:p.Glu1157del
NM_001127510.2:c.3468_3470del	NP_001120982.1:p.Glu1157del
NM_001127511.2:c.3414_3416del	NP_001120983.2:p.Glu1139del
NM_001354895.1:c.3468_3470del	NP_001341824.1:p.Glu1157del
NM_001354896.1:c.3522_3524del	NP_001341825.1:p.Glu1175del
NM_001354897.1:c.3498_3500del	NP_001341826.1:p.Glu1167del
NM_001354898.1:c.3393_3395del	NP_001341827.1:p.Glu1132del
NM_001354899.1:c.3384_3386del	NP_001341828.1:p.Glu1129del
NM_001354900.1:c.3345_3347del	NP_001341829.1:p.Glu1116del
NM_001354901.1:c.3291_3293del	NP_001341830.1:p.Glu1098del
NM_001354902.1:c.3195_3197del	NP_001341831.1:p.Glu1066del
NM_001354903.1:c.3165_3167del	NP_001341832.1:p.Glu1056del
NM_001354904.1:c.3090_3092del	NP_001341833.1:p.Glu1031del
NM_001354905.1:c.2988_2990del	NP_001341834.1:p.Glu997del
NM_001354906.1:c.2619_2621del	NP_001341835.1:p.Glu874del
NM_000038.6:c.3468_3470del MANE Select	NP_000029.2:p.Glu1157del
NM_001127510.3:c.3468_3470del	NP_001120982.1:p.Glu1157del
NM_001127511.3:c.3414_3416del	NP_001120983.2:p.Glu1139del
NM_001354895.2:c.3468_3470del	NP_001341824.1:p.Glu1157del
NM_001354896.2:c.3522_3524del	NP_001341825.1:p.Glu1175del
NM_001354897.2:c.3498_3500del	NP_001341826.1:p.Glu1167del
NM_001354898.2:c.3393_3395del	NP_001341827.1:p.Glu1132del
NM_001354899.2:c.3384_3386del	NP_001341828.1:p.Glu1129del
NM_001354900.2:c.3345_3347del	NP_001341829.1:p.Glu1116del
NM_001354901.2:c.3291_3293del	NP_001341830.1:p.Glu1098del
NM_001354902.2:c.3195_3197del	NP_001341831.1:p.Glu1066del
NM_001354903.2:c.3165_3167del	NP_001341832.1:p.Glu1056del
NM_001354904.2:c.3090_3092del	NP_001341833.1:p.Glu1031del
NM_001354905.2:c.2988_2990del	NP_001341834.1:p.Glu997del
NM_001354906.2:c.2619_2621del	NP_001341835.1:p.Glu874del