Canonical Allele Identifier: CA658760904

Gene: APC

Linked Data

• PubMed: PMID:8187091

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838912_112838913del , CM000667.2:g.112838912_112838913del	GRCh38
NC_000005.9:g.112174609_112174610del , CM000667.1:g.112174609_112174610del	GRCh37
NC_000005.8:g.112202508_112202509del	NCBI36
NG_008481.4:g.151392_151393del , LRG_130:g.151392_151393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2983_2984del	ENSP00000484935.2:n.2983_2984del
ENST00000504915.3:c.3372_3373del	ENSP00000473355.2:p.Ala1125GlnfsTer11
ENST00000505350.2:c.*3324_*3325del	ENSP00000481752.1:n.*3324_*3325del
ENST00000507379.6:c.3264_3265del	ENSP00000423224.2:p.Ala1089GlnfsTer11
ENST00000509732.6:c.3318_3319del	ENSP00000426541.2:p.Ala1107GlnfsTer11
ENST00000512211.7:c.3318_3319del	ENSP00000423828.3:p.Ala1107GlnfsTer11
ENST00000257430.9:c.3318_3319del MANE Select	ENSP00000257430.4:p.Ala1107GlnfsTer11
ENST00000257430.8:c.3318_3319del	ENSP00000257430.4:p.Ala1107GlnfsTer11
ENST00000502371.2:c.1671_1672del
ENST00000507379.5:c.3264_3265del	ENSP00000423224.1:p.Ala1089GlnfsTer11
ENST00000508376.6:c.3318_3319del	ENSP00000427089.2:p.Ala1107GlnfsTer11
ENST00000508624.5:c.*2640_*2641del	ENSP00000424265.1:n.*2640_*2641del
ENST00000512211.6:c.3318_3319del	ENSP00000423828.2:p.Ala1107GlnfsTer11
ENST00000520401.1:c.230+9940_230+9941del
NM_000038.5:c.3318_3319del	NP_000029.2:p.Ala1107GlnfsTer11
NM_001127510.2:c.3318_3319del	NP_001120982.1:p.Ala1107GlnfsTer11
NM_001127511.2:c.3264_3265del	NP_001120983.2:p.Ala1089GlnfsTer11
NM_001354895.1:c.3318_3319del	NP_001341824.1:p.Ala1107GlnfsTer11
NM_001354896.1:c.3372_3373del	NP_001341825.1:p.Ala1125GlnfsTer11
NM_001354897.1:c.3348_3349del	NP_001341826.1:p.Ala1117GlnfsTer11
NM_001354898.1:c.3243_3244del	NP_001341827.1:p.Ala1082GlnfsTer11
NM_001354899.1:c.3234_3235del	NP_001341828.1:p.Ala1079GlnfsTer11
NM_001354900.1:c.3195_3196del	NP_001341829.1:p.Ala1066GlnfsTer11
NM_001354901.1:c.3141_3142del	NP_001341830.1:p.Ala1048GlnfsTer11
NM_001354902.1:c.3045_3046del	NP_001341831.1:p.Ala1016GlnfsTer11
NM_001354903.1:c.3015_3016del	NP_001341832.1:p.Ala1006GlnfsTer11
NM_001354904.1:c.2940_2941del	NP_001341833.1:p.Ala981GlnfsTer11
NM_001354905.1:c.2838_2839del	NP_001341834.1:p.Ala947GlnfsTer11
NM_001354906.1:c.2469_2470del	NP_001341835.1:p.Ala824GlnfsTer11
NM_000038.6:c.3318_3319del MANE Select	NP_000029.2:p.Ala1107GlnfsTer11
NM_001127510.3:c.3318_3319del	NP_001120982.1:p.Ala1107GlnfsTer11
NM_001127511.3:c.3264_3265del	NP_001120983.2:p.Ala1089GlnfsTer11
NM_001354895.2:c.3318_3319del	NP_001341824.1:p.Ala1107GlnfsTer11
NM_001354896.2:c.3372_3373del	NP_001341825.1:p.Ala1125GlnfsTer11
NM_001354897.2:c.3348_3349del	NP_001341826.1:p.Ala1117GlnfsTer11
NM_001354898.2:c.3243_3244del	NP_001341827.1:p.Ala1082GlnfsTer11
NM_001354899.2:c.3234_3235del	NP_001341828.1:p.Ala1079GlnfsTer11
NM_001354900.2:c.3195_3196del	NP_001341829.1:p.Ala1066GlnfsTer11
NM_001354901.2:c.3141_3142del	NP_001341830.1:p.Ala1048GlnfsTer11
NM_001354902.2:c.3045_3046del	NP_001341831.1:p.Ala1016GlnfsTer11
NM_001354903.2:c.3015_3016del	NP_001341832.1:p.Ala1006GlnfsTer11
NM_001354904.2:c.2940_2941del	NP_001341833.1:p.Ala981GlnfsTer11
NM_001354905.2:c.2838_2839del	NP_001341834.1:p.Ala947GlnfsTer11
NM_001354906.2:c.2469_2470del	NP_001341835.1:p.Ala824GlnfsTer11