Canonical Allele Identifier: CA658760903

Gene: APC

Linked Data

• PubMed: PMID:11247896

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838910_112838913dup , CM000667.2:g.112838910_112838913dup	GRCh38
NC_000005.9:g.112174607_112174610dup , CM000667.1:g.112174607_112174610dup	GRCh37
NC_000005.8:g.112202506_112202509dup	NCBI36
NG_008481.4:g.151390_151393dup , LRG_130:g.151390_151393dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2981_2984dup	ENSP00000484935.2:n.2981_2984dup
ENST00000504915.3:c.3370_3373dup	ENSP00000473355.2:p.Ala1125GlyfsTer13
ENST00000505350.2:c.*3322_*3325dup	ENSP00000481752.1:n.*3322_*3325dup
ENST00000507379.6:c.3262_3265dup	ENSP00000423224.2:p.Ala1089GlyfsTer13
ENST00000509732.6:c.3316_3319dup	ENSP00000426541.2:p.Ala1107GlyfsTer13
ENST00000512211.7:c.3316_3319dup	ENSP00000423828.3:p.Ala1107GlyfsTer13
ENST00000257430.9:c.3316_3319dup MANE Select	ENSP00000257430.4:p.Ala1107GlyfsTer13
ENST00000257430.8:c.3316_3319dup	ENSP00000257430.4:p.Ala1107GlyfsTer13
ENST00000502371.2:c.1669_1672dup
ENST00000507379.5:c.3262_3265dup	ENSP00000423224.1:p.Ala1089GlyfsTer13
ENST00000508376.6:c.3316_3319dup	ENSP00000427089.2:p.Ala1107GlyfsTer13
ENST00000508624.5:c.*2638_*2641dup	ENSP00000424265.1:n.*2638_*2641dup
ENST00000512211.6:c.3316_3319dup	ENSP00000423828.2:p.Ala1107GlyfsTer13
ENST00000520401.1:c.230+9938_230+9941dup
NM_000038.5:c.3316_3319dup	NP_000029.2:p.Ala1107GlyfsTer13
NM_001127510.2:c.3316_3319dup	NP_001120982.1:p.Ala1107GlyfsTer13
NM_001127511.2:c.3262_3265dup	NP_001120983.2:p.Ala1089GlyfsTer13
NM_001354895.1:c.3316_3319dup	NP_001341824.1:p.Ala1107GlyfsTer13
NM_001354896.1:c.3370_3373dup	NP_001341825.1:p.Ala1125GlyfsTer13
NM_001354897.1:c.3346_3349dup	NP_001341826.1:p.Ala1117GlyfsTer13
NM_001354898.1:c.3241_3244dup	NP_001341827.1:p.Ala1082GlyfsTer13
NM_001354899.1:c.3232_3235dup	NP_001341828.1:p.Ala1079GlyfsTer13
NM_001354900.1:c.3193_3196dup	NP_001341829.1:p.Ala1066GlyfsTer13
NM_001354901.1:c.3139_3142dup	NP_001341830.1:p.Ala1048GlyfsTer13
NM_001354902.1:c.3043_3046dup	NP_001341831.1:p.Ala1016GlyfsTer13
NM_001354903.1:c.3013_3016dup	NP_001341832.1:p.Ala1006GlyfsTer13
NM_001354904.1:c.2938_2941dup	NP_001341833.1:p.Ala981GlyfsTer13
NM_001354905.1:c.2836_2839dup	NP_001341834.1:p.Ala947GlyfsTer13
NM_001354906.1:c.2467_2470dup	NP_001341835.1:p.Ala824GlyfsTer13
NM_000038.6:c.3316_3319dup MANE Select	NP_000029.2:p.Ala1107GlyfsTer13
NM_001127510.3:c.3316_3319dup	NP_001120982.1:p.Ala1107GlyfsTer13
NM_001127511.3:c.3262_3265dup	NP_001120983.2:p.Ala1089GlyfsTer13
NM_001354895.2:c.3316_3319dup	NP_001341824.1:p.Ala1107GlyfsTer13
NM_001354896.2:c.3370_3373dup	NP_001341825.1:p.Ala1125GlyfsTer13
NM_001354897.2:c.3346_3349dup	NP_001341826.1:p.Ala1117GlyfsTer13
NM_001354898.2:c.3241_3244dup	NP_001341827.1:p.Ala1082GlyfsTer13
NM_001354899.2:c.3232_3235dup	NP_001341828.1:p.Ala1079GlyfsTer13
NM_001354900.2:c.3193_3196dup	NP_001341829.1:p.Ala1066GlyfsTer13
NM_001354901.2:c.3139_3142dup	NP_001341830.1:p.Ala1048GlyfsTer13
NM_001354902.2:c.3043_3046dup	NP_001341831.1:p.Ala1016GlyfsTer13
NM_001354903.2:c.3013_3016dup	NP_001341832.1:p.Ala1006GlyfsTer13
NM_001354904.2:c.2938_2941dup	NP_001341833.1:p.Ala981GlyfsTer13
NM_001354905.2:c.2836_2839dup	NP_001341834.1:p.Ala947GlyfsTer13
NM_001354906.2:c.2467_2470dup	NP_001341835.1:p.Ala824GlyfsTer13