Canonical Allele Identifier: CA645372792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433655
ClinVar RCV Id: RCV000501272
dbSNP Id: rs1554085335

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839421_112839423delinsA , CM000667.2:g.112839421_112839423delinsA GRCh38
NC_000005.9:g.112175118_112175120delinsA , CM000667.1:g.112175118_112175120delinsA GRCh37
NC_000005.8:g.112203017_112203019delinsA NCBI36
NG_008481.4:g.151901_151903delinsA , LRG_130:g.151901_151903delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.3492_3494delinsA ENSP00000484935.2:n.3492_3494delinsA
ENST00000504915.3:c.3881_3883delinsA ENSP00000473355.2:p.Ser1294TyrfsTer8
ENST00000505350.2:c.*3833_*3835delinsA ENSP00000481752.1:n.*3833_*3835delinsA
ENST00000507379.6:c.3773_3775delinsA ENSP00000423224.2:p.Ser1258TyrfsTer8
ENST00000509732.6:c.3827_3829delinsA ENSP00000426541.2:p.Ser1276TyrfsTer8
ENST00000512211.7:c.3827_3829delinsA ENSP00000423828.3:p.Ser1276TyrfsTer8
ENST00000257430.9:c.3827_3829delinsA MANE Select ENSP00000257430.4:p.Ser1276TyrfsTer8
ENST00000257430.8:c.3827_3829delinsA ENSP00000257430.4:p.Ser1276TyrfsTer8
ENST00000502371.2:c.2180_2182delinsA
ENST00000508376.6:c.3827_3829delinsA ENSP00000427089.2:p.Ser1276TyrfsTer8
ENST00000508624.5:c.*3149_*3151delinsA ENSP00000424265.1:n.*3149_*3151delinsA
ENST00000512211.6:c.3827_3829delinsA ENSP00000423828.2:p.Ser1276TyrfsTer8
ENST00000520401.1:c.230+10449_230+10451delinsA
NM_000038.5:c.3827_3829delinsA NP_000029.2:p.Ser1276TyrfsTer8
NM_001127510.2:c.3827_3829delinsA NP_001120982.1:p.Ser1276TyrfsTer8
NM_001127511.2:c.3773_3775delinsA NP_001120983.2:p.Ser1258TyrfsTer8
NM_001354895.1:c.3827_3829delinsA NP_001341824.1:p.Ser1276TyrfsTer8
NM_001354896.1:c.3881_3883delinsA NP_001341825.1:p.Ser1294TyrfsTer8
NM_001354897.1:c.3857_3859delinsA NP_001341826.1:p.Ser1286TyrfsTer8
NM_001354898.1:c.3752_3754delinsA NP_001341827.1:p.Ser1251TyrfsTer8
NM_001354899.1:c.3743_3745delinsA NP_001341828.1:p.Ser1248TyrfsTer8
NM_001354900.1:c.3704_3706delinsA NP_001341829.1:p.Ser1235TyrfsTer8
NM_001354901.1:c.3650_3652delinsA NP_001341830.1:p.Ser1217TyrfsTer8
NM_001354902.1:c.3554_3556delinsA NP_001341831.1:p.Ser1185TyrfsTer8
NM_001354903.1:c.3524_3526delinsA NP_001341832.1:p.Ser1175TyrfsTer8
NM_001354904.1:c.3449_3451delinsA NP_001341833.1:p.Ser1150TyrfsTer8
NM_001354905.1:c.3347_3349delinsA NP_001341834.1:p.Ser1116TyrfsTer8
NM_001354906.1:c.2978_2980delinsA NP_001341835.1:p.Ser993TyrfsTer8
NM_000038.6:c.3827_3829delinsA MANE Select NP_000029.2:p.Ser1276TyrfsTer8
NM_001127510.3:c.3827_3829delinsA NP_001120982.1:p.Ser1276TyrfsTer8
NM_001127511.3:c.3773_3775delinsA NP_001120983.2:p.Ser1258TyrfsTer8
NM_001354895.2:c.3827_3829delinsA NP_001341824.1:p.Ser1276TyrfsTer8
NM_001354896.2:c.3881_3883delinsA NP_001341825.1:p.Ser1294TyrfsTer8
NM_001354897.2:c.3857_3859delinsA NP_001341826.1:p.Ser1286TyrfsTer8
NM_001354898.2:c.3752_3754delinsA NP_001341827.1:p.Ser1251TyrfsTer8
NM_001354899.2:c.3743_3745delinsA NP_001341828.1:p.Ser1248TyrfsTer8
NM_001354900.2:c.3704_3706delinsA NP_001341829.1:p.Ser1235TyrfsTer8
NM_001354901.2:c.3650_3652delinsA NP_001341830.1:p.Ser1217TyrfsTer8
NM_001354902.2:c.3554_3556delinsA NP_001341831.1:p.Ser1185TyrfsTer8
NM_001354903.2:c.3524_3526delinsA NP_001341832.1:p.Ser1175TyrfsTer8
NM_001354904.2:c.3449_3451delinsA NP_001341833.1:p.Ser1150TyrfsTer8
NM_001354905.2:c.3347_3349delinsA NP_001341834.1:p.Ser1116TyrfsTer8
NM_001354906.2:c.2978_2980delinsA NP_001341835.1:p.Ser993TyrfsTer8