Canonical Allele Identifier: CA2695204936

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839007_112839011del , CM000667.2:g.112839007_112839011del	GRCh38
NC_000005.9:g.112174704_112174708del , CM000667.1:g.112174704_112174708del	GRCh37
NC_000005.8:g.112202603_112202607del	NCBI36
NG_008481.4:g.151487_151491del , LRG_130:g.151487_151491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3078_3082del	ENSP00000484935.2:n.3078_3082del
ENST00000504915.3:c.3467_3471del	ENSP00000473355.2:p.Asp1156AlafsTer5
ENST00000505350.2:c.*3419_*3423del	ENSP00000481752.1:n.*3419_*3423del
ENST00000507379.6:c.3359_3363del	ENSP00000423224.2:p.Asp1120AlafsTer5
ENST00000509732.6:c.3413_3417del	ENSP00000426541.2:p.Asp1138AlafsTer5
ENST00000512211.7:c.3413_3417del	ENSP00000423828.3:p.Asp1138AlafsTer5
ENST00000257430.9:c.3413_3417del MANE Select	ENSP00000257430.4:p.Asp1138AlafsTer5
ENST00000257430.8:c.3413_3417del	ENSP00000257430.4:p.Asp1138AlafsTer5
ENST00000502371.2:c.1766_1770del
ENST00000507379.5:c.3359_3363del	ENSP00000423224.1:p.Asp1120AlafsTer5
ENST00000508376.6:c.3413_3417del	ENSP00000427089.2:p.Asp1138AlafsTer5
ENST00000508624.5:c.*2735_*2739del	ENSP00000424265.1:n.*2735_*2739del
ENST00000512211.6:c.3413_3417del	ENSP00000423828.2:p.Asp1138AlafsTer5
ENST00000520401.1:c.230+10035_230+10039del
NM_000038.5:c.3413_3417del	NP_000029.2:p.Asp1138AlafsTer5
NM_001127510.2:c.3413_3417del	NP_001120982.1:p.Asp1138AlafsTer5
NM_001127511.2:c.3359_3363del	NP_001120983.2:p.Asp1120AlafsTer5
NM_001354895.1:c.3413_3417del	NP_001341824.1:p.Asp1138AlafsTer5
NM_001354896.1:c.3467_3471del	NP_001341825.1:p.Asp1156AlafsTer5
NM_001354897.1:c.3443_3447del	NP_001341826.1:p.Asp1148AlafsTer5
NM_001354898.1:c.3338_3342del	NP_001341827.1:p.Asp1113AlafsTer5
NM_001354899.1:c.3329_3333del	NP_001341828.1:p.Asp1110AlafsTer5
NM_001354900.1:c.3290_3294del	NP_001341829.1:p.Asp1097AlafsTer5
NM_001354901.1:c.3236_3240del	NP_001341830.1:p.Asp1079AlafsTer5
NM_001354902.1:c.3140_3144del	NP_001341831.1:p.Asp1047AlafsTer5
NM_001354903.1:c.3110_3114del	NP_001341832.1:p.Asp1037AlafsTer5
NM_001354904.1:c.3035_3039del	NP_001341833.1:p.Asp1012AlafsTer5
NM_001354905.1:c.2933_2937del	NP_001341834.1:p.Asp978AlafsTer5
NM_001354906.1:c.2564_2568del	NP_001341835.1:p.Asp855AlafsTer5
NM_000038.6:c.3413_3417del MANE Select	NP_000029.2:p.Asp1138AlafsTer5
NM_001127510.3:c.3413_3417del	NP_001120982.1:p.Asp1138AlafsTer5
NM_001127511.3:c.3359_3363del	NP_001120983.2:p.Asp1120AlafsTer5
NM_001354895.2:c.3413_3417del	NP_001341824.1:p.Asp1138AlafsTer5
NM_001354896.2:c.3467_3471del	NP_001341825.1:p.Asp1156AlafsTer5
NM_001354897.2:c.3443_3447del	NP_001341826.1:p.Asp1148AlafsTer5
NM_001354898.2:c.3338_3342del	NP_001341827.1:p.Asp1113AlafsTer5
NM_001354899.2:c.3329_3333del	NP_001341828.1:p.Asp1110AlafsTer5
NM_001354900.2:c.3290_3294del	NP_001341829.1:p.Asp1097AlafsTer5
NM_001354901.2:c.3236_3240del	NP_001341830.1:p.Asp1079AlafsTer5
NM_001354902.2:c.3140_3144del	NP_001341831.1:p.Asp1047AlafsTer5
NM_001354903.2:c.3110_3114del	NP_001341832.1:p.Asp1037AlafsTer5
NM_001354904.2:c.3035_3039del	NP_001341833.1:p.Asp1012AlafsTer5
NM_001354905.2:c.2933_2937del	NP_001341834.1:p.Asp978AlafsTer5
NM_001354906.2:c.2564_2568del	NP_001341835.1:p.Asp855AlafsTer5