Canonical Allele Identifier: CA046911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390
dbSNP Id: rs772778630

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112842693A>G , CM000667.2:g.112842693A>G GRCh38
NC_000005.9:g.112178390A>G , CM000667.1:g.112178390A>G GRCh37
NC_000005.8:g.112206289A>G NCBI36
NG_008481.4:g.155173A>G , LRG_130:g.155173A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7153A>G ENSP00000473355.2:p.Thr2385Ala
ENST00000505350.2:c.*7105A>G ENSP00000481752.1:n.*7105A>G
ENST00000507379.6:c.7045A>G ENSP00000423224.2:p.Thr2349Ala
ENST00000509732.6:c.7099A>G ENSP00000426541.2:p.Thr2367Ala
ENST00000512211.7:c.7099A>G ENSP00000423828.3:p.Thr2367Ala
ENST00000257430.9:c.7099A>G MANE Select ENSP00000257430.4:p.Thr2367Ala
ENST00000257430.8:c.7099A>G ENSP00000257430.4:p.Thr2367Ala
ENST00000508376.6:c.7099A>G ENSP00000427089.2:p.Thr2367Ala
ENST00000508624.5:c.*6421A>G ENSP00000424265.1:n.*6421A>G
ENST00000520401.1:c.230+13721A>G
NM_000038.5:c.7099A>G NP_000029.2:p.Thr2367Ala
NM_001127510.2:c.7099A>G NP_001120982.1:p.Thr2367Ala
NM_001127511.2:c.7045A>G NP_001120983.2:p.Thr2349Ala
NM_001354895.1:c.7099A>G NP_001341824.1:p.Thr2367Ala
NM_001354896.1:c.7153A>G NP_001341825.1:p.Thr2385Ala
NM_001354897.1:c.7129A>G NP_001341826.1:p.Thr2377Ala
NM_001354898.1:c.7024A>G NP_001341827.1:p.Thr2342Ala
NM_001354899.1:c.7015A>G NP_001341828.1:p.Thr2339Ala
NM_001354900.1:c.6976A>G NP_001341829.1:p.Thr2326Ala
NM_001354901.1:c.6922A>G NP_001341830.1:p.Thr2308Ala
NM_001354902.1:c.6826A>G NP_001341831.1:p.Thr2276Ala
NM_001354903.1:c.6796A>G NP_001341832.1:p.Thr2266Ala
NM_001354904.1:c.6721A>G NP_001341833.1:p.Thr2241Ala
NM_001354905.1:c.6619A>G NP_001341834.1:p.Thr2207Ala
NM_001354906.1:c.6250A>G NP_001341835.1:p.Thr2084Ala
NM_000038.6:c.7099A>G MANE Select NP_000029.2:p.Thr2367Ala
NM_001127510.3:c.7099A>G NP_001120982.1:p.Thr2367Ala
NM_001127511.3:c.7045A>G NP_001120983.2:p.Thr2349Ala
NM_001354895.2:c.7099A>G NP_001341824.1:p.Thr2367Ala
NM_001354896.2:c.7153A>G NP_001341825.1:p.Thr2385Ala
NM_001354897.2:c.7129A>G NP_001341826.1:p.Thr2377Ala
NM_001354898.2:c.7024A>G NP_001341827.1:p.Thr2342Ala
NM_001354899.2:c.7015A>G NP_001341828.1:p.Thr2339Ala
NM_001354900.2:c.6976A>G NP_001341829.1:p.Thr2326Ala
NM_001354901.2:c.6922A>G NP_001341830.1:p.Thr2308Ala
NM_001354902.2:c.6826A>G NP_001341831.1:p.Thr2276Ala
NM_001354903.2:c.6796A>G NP_001341832.1:p.Thr2266Ala
NM_001354904.2:c.6721A>G NP_001341833.1:p.Thr2241Ala
NM_001354905.2:c.6619A>G NP_001341834.1:p.Thr2207Ala
NM_001354906.2:c.6250A>G NP_001341835.1:p.Thr2084Ala