Canonical Allele Identifier: CA009712
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140839
dbSNP Id: rs138367627

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840326T>G , CM000667.2:g.112840326T>G GRCh38
NC_000005.9:g.112176023T>G , CM000667.1:g.112176023T>G GRCh37
NC_000005.8:g.112203922T>G NCBI36
NG_008481.4:g.152806T>G , LRG_130:g.152806T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000504915.3:c.4786T>G ENSP00000473355.2:p.Cys1596Gly
ENST00000505350.2:c.*4738T>G ENSP00000481752.1:n.*4738T>G
ENST00000507379.6:c.4678T>G ENSP00000423224.2:p.Cys1560Gly
ENST00000509732.6:c.4732T>G ENSP00000426541.2:p.Cys1578Gly
ENST00000512211.7:c.4732T>G ENSP00000423828.3:p.Cys1578Gly
ENST00000257430.9:c.4732T>G MANE Select ENSP00000257430.4:p.Cys1578Gly
ENST00000257430.8:c.4732T>G ENSP00000257430.4:p.Cys1578Gly
ENST00000508376.6:c.4732T>G ENSP00000427089.2:p.Cys1578Gly
ENST00000508624.5:c.*4054T>G ENSP00000424265.1:n.*4054T>G
ENST00000520401.1:c.230+11354T>G
NM_000038.5:c.4732T>G NP_000029.2:p.Cys1578Gly
NM_001127510.2:c.4732T>G NP_001120982.1:p.Cys1578Gly
NM_001127511.2:c.4678T>G NP_001120983.2:p.Cys1560Gly
NM_001354895.1:c.4732T>G NP_001341824.1:p.Cys1578Gly
NM_001354896.1:c.4786T>G NP_001341825.1:p.Cys1596Gly
NM_001354897.1:c.4762T>G NP_001341826.1:p.Cys1588Gly
NM_001354898.1:c.4657T>G NP_001341827.1:p.Cys1553Gly
NM_001354899.1:c.4648T>G NP_001341828.1:p.Cys1550Gly
NM_001354900.1:c.4609T>G NP_001341829.1:p.Cys1537Gly
NM_001354901.1:c.4555T>G NP_001341830.1:p.Cys1519Gly
NM_001354902.1:c.4459T>G NP_001341831.1:p.Cys1487Gly
NM_001354903.1:c.4429T>G NP_001341832.1:p.Cys1477Gly
NM_001354904.1:c.4354T>G NP_001341833.1:p.Cys1452Gly
NM_001354905.1:c.4252T>G NP_001341834.1:p.Cys1418Gly
NM_001354906.1:c.3883T>G NP_001341835.1:p.Cys1295Gly
NM_000038.6:c.4732T>G MANE Select NP_000029.2:p.Cys1578Gly
NM_001127510.3:c.4732T>G NP_001120982.1:p.Cys1578Gly
NM_001127511.3:c.4678T>G NP_001120983.2:p.Cys1560Gly
NM_001354895.2:c.4732T>G NP_001341824.1:p.Cys1578Gly
NM_001354896.2:c.4786T>G NP_001341825.1:p.Cys1596Gly
NM_001354897.2:c.4762T>G NP_001341826.1:p.Cys1588Gly
NM_001354898.2:c.4657T>G NP_001341827.1:p.Cys1553Gly
NM_001354899.2:c.4648T>G NP_001341828.1:p.Cys1550Gly
NM_001354900.2:c.4609T>G NP_001341829.1:p.Cys1537Gly
NM_001354901.2:c.4555T>G NP_001341830.1:p.Cys1519Gly
NM_001354902.2:c.4459T>G NP_001341831.1:p.Cys1487Gly
NM_001354903.2:c.4429T>G NP_001341832.1:p.Cys1477Gly
NM_001354904.2:c.4354T>G NP_001341833.1:p.Cys1452Gly
NM_001354905.2:c.4252T>G NP_001341834.1:p.Cys1418Gly
NM_001354906.2:c.3883T>G NP_001341835.1:p.Cys1295Gly