Canonical Allele Identifier: CA014059
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142442
dbSNP Id: rs138137162

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843380T>G , CM000667.2:g.112843380T>G GRCh38
NC_000005.9:g.112179077T>G , CM000667.1:g.112179077T>G GRCh37
NC_000005.8:g.112206976T>G NCBI36
NG_008481.4:g.155860T>G , LRG_130:g.155860T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7840T>G ENSP00000473355.2:p.Ser2614Ala
ENST00000505350.2:c.*7792T>G ENSP00000481752.1:n.*7792T>G
ENST00000507379.6:c.7732T>G ENSP00000423224.2:p.Ser2578Ala
ENST00000509732.6:c.7786T>G ENSP00000426541.2:p.Ser2596Ala
ENST00000512211.7:c.7786T>G ENSP00000423828.3:p.Ser2596Ala
ENST00000257430.9:c.7786T>G MANE Select ENSP00000257430.4:p.Ser2596Ala
ENST00000257430.8:c.7786T>G ENSP00000257430.4:p.Ser2596Ala
ENST00000508376.6:c.7786T>G ENSP00000427089.2:p.Ser2596Ala
ENST00000520401.1:c.231-13269T>G
NM_000038.5:c.7786T>G NP_000029.2:p.Ser2596Ala
NM_001127510.2:c.7786T>G NP_001120982.1:p.Ser2596Ala
NM_001127511.2:c.7732T>G NP_001120983.2:p.Ser2578Ala
NM_001354895.1:c.7786T>G NP_001341824.1:p.Ser2596Ala
NM_001354896.1:c.7840T>G NP_001341825.1:p.Ser2614Ala
NM_001354897.1:c.7816T>G NP_001341826.1:p.Ser2606Ala
NM_001354898.1:c.7711T>G NP_001341827.1:p.Ser2571Ala
NM_001354899.1:c.7702T>G NP_001341828.1:p.Ser2568Ala
NM_001354900.1:c.7663T>G NP_001341829.1:p.Ser2555Ala
NM_001354901.1:c.7609T>G NP_001341830.1:p.Ser2537Ala
NM_001354902.1:c.7513T>G NP_001341831.1:p.Ser2505Ala
NM_001354903.1:c.7483T>G NP_001341832.1:p.Ser2495Ala
NM_001354904.1:c.7408T>G NP_001341833.1:p.Ser2470Ala
NM_001354905.1:c.7306T>G NP_001341834.1:p.Ser2436Ala
NM_001354906.1:c.6937T>G NP_001341835.1:p.Ser2313Ala
NM_000038.6:c.7786T>G MANE Select NP_000029.2:p.Ser2596Ala
NM_001127510.3:c.7786T>G NP_001120982.1:p.Ser2596Ala
NM_001127511.3:c.7732T>G NP_001120983.2:p.Ser2578Ala
NM_001354895.2:c.7786T>G NP_001341824.1:p.Ser2596Ala
NM_001354896.2:c.7840T>G NP_001341825.1:p.Ser2614Ala
NM_001354897.2:c.7816T>G NP_001341826.1:p.Ser2606Ala
NM_001354898.2:c.7711T>G NP_001341827.1:p.Ser2571Ala
NM_001354899.2:c.7702T>G NP_001341828.1:p.Ser2568Ala
NM_001354900.2:c.7663T>G NP_001341829.1:p.Ser2555Ala
NM_001354901.2:c.7609T>G NP_001341830.1:p.Ser2537Ala
NM_001354902.2:c.7513T>G NP_001341831.1:p.Ser2505Ala
NM_001354903.2:c.7483T>G NP_001341832.1:p.Ser2495Ala
NM_001354904.2:c.7408T>G NP_001341833.1:p.Ser2470Ala
NM_001354905.2:c.7306T>G NP_001341834.1:p.Ser2436Ala
NM_001354906.2:c.6937T>G NP_001341835.1:p.Ser2313Ala