Canonical Allele Identifier: CA16618087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421962
ClinVar RCV Id: RCV000485953
dbSNP Id: rs1064795475

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840372_112840373insT , CM000667.2:g.112840372_112840373insT GRCh38
NC_000005.9:g.112176069_112176070insT , CM000667.1:g.112176069_112176070insT GRCh37
NC_000005.8:g.112203968_112203969insT NCBI36
NG_008481.4:g.152852_152853insT , LRG_130:g.152852_152853insT

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.4832_4833insT ENSP00000473355.2:p.Lys1611AsnfsTer?
ENST00000505350.2:c.*4784_*4785insT ENSP00000481752.1:n.*4784_*4785insT
ENST00000507379.6:c.4724_4725insT ENSP00000423224.2:p.Lys1575AsnfsTer?
ENST00000509732.6:c.4778_4779insT ENSP00000426541.2:p.Lys1593AsnfsTer?
ENST00000512211.7:c.4778_4779insT ENSP00000423828.3:p.Lys1593AsnfsTer?
ENST00000257430.9:c.4778_4779insT MANE Select ENSP00000257430.4:p.Lys1593AsnfsTer?
ENST00000257430.8:c.4778_4779insT ENSP00000257430.4:p.Lys1593AsnfsTer?
ENST00000508376.6:c.4778_4779insT ENSP00000427089.2:p.Lys1593AsnfsTer?
ENST00000508624.5:c.*4100_*4101insT ENSP00000424265.1:n.*4100_*4101insT
ENST00000520401.1:c.230+11400_230+11401insT
NM_000038.5:c.4778_4779insT NP_000029.2:p.Lys1593AsnfsTer?
NM_001127510.2:c.4778_4779insT NP_001120982.1:p.Lys1593AsnfsTer?
NM_001127511.2:c.4724_4725insT NP_001120983.2:p.Lys1575AsnfsTer?
NM_001354895.1:c.4778_4779insT NP_001341824.1:p.Lys1593AsnfsTer?
NM_001354896.1:c.4832_4833insT NP_001341825.1:p.Lys1611AsnfsTer?
NM_001354897.1:c.4808_4809insT NP_001341826.1:p.Lys1603AsnfsTer?
NM_001354898.1:c.4703_4704insT NP_001341827.1:p.Lys1568AsnfsTer?
NM_001354899.1:c.4694_4695insT NP_001341828.1:p.Lys1565AsnfsTer?
NM_001354900.1:c.4655_4656insT NP_001341829.1:p.Lys1552AsnfsTer?
NM_001354901.1:c.4601_4602insT NP_001341830.1:p.Lys1534AsnfsTer?
NM_001354902.1:c.4505_4506insT NP_001341831.1:p.Lys1502AsnfsTer?
NM_001354903.1:c.4475_4476insT NP_001341832.1:p.Lys1492AsnfsTer?
NM_001354904.1:c.4400_4401insT NP_001341833.1:p.Lys1467AsnfsTer?
NM_001354905.1:c.4298_4299insT NP_001341834.1:p.Lys1433AsnfsTer?
NM_001354906.1:c.3929_3930insT NP_001341835.1:p.Lys1310AsnfsTer?
NM_000038.6:c.4778_4779insT MANE Select NP_000029.2:p.Lys1593AsnfsTer?
NM_001127510.3:c.4778_4779insT NP_001120982.1:p.Lys1593AsnfsTer?
NM_001127511.3:c.4724_4725insT NP_001120983.2:p.Lys1575AsnfsTer?
NM_001354895.2:c.4778_4779insT NP_001341824.1:p.Lys1593AsnfsTer?
NM_001354896.2:c.4832_4833insT NP_001341825.1:p.Lys1611AsnfsTer?
NM_001354897.2:c.4808_4809insT NP_001341826.1:p.Lys1603AsnfsTer?
NM_001354898.2:c.4703_4704insT NP_001341827.1:p.Lys1568AsnfsTer?
NM_001354899.2:c.4694_4695insT NP_001341828.1:p.Lys1565AsnfsTer?
NM_001354900.2:c.4655_4656insT NP_001341829.1:p.Lys1552AsnfsTer?
NM_001354901.2:c.4601_4602insT NP_001341830.1:p.Lys1534AsnfsTer?
NM_001354902.2:c.4505_4506insT NP_001341831.1:p.Lys1502AsnfsTer?
NM_001354903.2:c.4475_4476insT NP_001341832.1:p.Lys1492AsnfsTer?
NM_001354904.2:c.4400_4401insT NP_001341833.1:p.Lys1467AsnfsTer?
NM_001354905.2:c.4298_4299insT NP_001341834.1:p.Lys1433AsnfsTer?
NM_001354906.2:c.3929_3930insT NP_001341835.1:p.Lys1310AsnfsTer?