Canonical Allele Identifier: CA16611649
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411529
ClinVar RCV Id: RCV003153638
dbSNP Id: rs1064792979
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839951_112839957delinsAAT , CM000667.2:g.112839951_112839957delinsAAT GRCh38
NC_000005.9:g.112175648_112175654delinsAAT , CM000667.1:g.112175648_112175654delinsAAT GRCh37
NC_000005.8:g.112203547_112203553delinsAAT NCBI36
NG_008481.4:g.152431_152437delinsAAT , LRG_130:g.152431_152437delinsAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.4411_4417delinsAAT ENSP00000473355.2:p.Pro1471AsnfsTer19
ENST00000505350.2:c.*4363_*4369delinsAAT ENSP00000481752.1:n.*4363_*4369delinsAAT
ENST00000507379.6:c.4303_4309delinsAAT ENSP00000423224.2:p.Pro1435AsnfsTer19
ENST00000509732.6:c.4357_4363delinsAAT ENSP00000426541.2:p.Pro1453AsnfsTer19
ENST00000512211.7:c.4357_4363delinsAAT ENSP00000423828.3:p.Pro1453AsnfsTer19
ENST00000257430.9:c.4357_4363delinsAAT MANE Select ENSP00000257430.4:p.Pro1453AsnfsTer19
ENST00000257430.8:c.4357_4363delinsAAT ENSP00000257430.4:p.Pro1453AsnfsTer19
ENST00000508376.6:c.4357_4363delinsAAT ENSP00000427089.2:p.Pro1453AsnfsTer19
ENST00000508624.5:c.*3679_*3685delinsAAT ENSP00000424265.1:n.*3679_*3685delinsAAT
ENST00000520401.1:c.230+10979_230+10985delinsAAT
NM_000038.5:c.4357_4363delinsAAT NP_000029.2:p.Pro1453AsnfsTer19
NM_001127510.2:c.4357_4363delinsAAT NP_001120982.1:p.Pro1453AsnfsTer19
NM_001127511.2:c.4303_4309delinsAAT NP_001120983.2:p.Pro1435AsnfsTer19
NM_001354895.1:c.4357_4363delinsAAT NP_001341824.1:p.Pro1453AsnfsTer19
NM_001354896.1:c.4411_4417delinsAAT NP_001341825.1:p.Pro1471AsnfsTer19
NM_001354897.1:c.4387_4393delinsAAT NP_001341826.1:p.Pro1463AsnfsTer19
NM_001354898.1:c.4282_4288delinsAAT NP_001341827.1:p.Pro1428AsnfsTer19
NM_001354899.1:c.4273_4279delinsAAT NP_001341828.1:p.Pro1425AsnfsTer19
NM_001354900.1:c.4234_4240delinsAAT NP_001341829.1:p.Pro1412AsnfsTer19
NM_001354901.1:c.4180_4186delinsAAT NP_001341830.1:p.Pro1394AsnfsTer19
NM_001354902.1:c.4084_4090delinsAAT NP_001341831.1:p.Pro1362AsnfsTer19
NM_001354903.1:c.4054_4060delinsAAT NP_001341832.1:p.Pro1352AsnfsTer19
NM_001354904.1:c.3979_3985delinsAAT NP_001341833.1:p.Pro1327AsnfsTer19
NM_001354905.1:c.3877_3883delinsAAT NP_001341834.1:p.Pro1293AsnfsTer19
NM_001354906.1:c.3508_3514delinsAAT NP_001341835.1:p.Pro1170AsnfsTer19
NM_000038.6:c.4357_4363delinsAAT MANE Select NP_000029.2:p.Pro1453AsnfsTer19
NM_001127510.3:c.4357_4363delinsAAT NP_001120982.1:p.Pro1453AsnfsTer19
NM_001127511.3:c.4303_4309delinsAAT NP_001120983.2:p.Pro1435AsnfsTer19
NM_001354895.2:c.4357_4363delinsAAT NP_001341824.1:p.Pro1453AsnfsTer19
NM_001354896.2:c.4411_4417delinsAAT NP_001341825.1:p.Pro1471AsnfsTer19
NM_001354897.2:c.4387_4393delinsAAT NP_001341826.1:p.Pro1463AsnfsTer19
NM_001354898.2:c.4282_4288delinsAAT NP_001341827.1:p.Pro1428AsnfsTer19
NM_001354899.2:c.4273_4279delinsAAT NP_001341828.1:p.Pro1425AsnfsTer19
NM_001354900.2:c.4234_4240delinsAAT NP_001341829.1:p.Pro1412AsnfsTer19
NM_001354901.2:c.4180_4186delinsAAT NP_001341830.1:p.Pro1394AsnfsTer19
NM_001354902.2:c.4084_4090delinsAAT NP_001341831.1:p.Pro1362AsnfsTer19
NM_001354903.2:c.4054_4060delinsAAT NP_001341832.1:p.Pro1352AsnfsTer19
NM_001354904.2:c.3979_3985delinsAAT NP_001341833.1:p.Pro1327AsnfsTer19
NM_001354905.2:c.3877_3883delinsAAT NP_001341834.1:p.Pro1293AsnfsTer19
NM_001354906.2:c.3508_3514delinsAAT NP_001341835.1:p.Pro1170AsnfsTer19
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