Canonical Allele Identifier: CA446211003
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs1554088819
COSMIC: COSM448438
MyVariant Identifiers: chr5:g.112179286C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843589C>G , CM000667.2:g.112843589C>G GRCh38
NC_000005.9:g.112179286C>G , CM000667.1:g.112179286C>G GRCh37
NC_000005.8:g.112207185C>G NCBI36
NG_008481.4:g.156069C>G , LRG_130:g.156069C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8049C>G ENSP00000473355.2:p.Pro2683=
ENST00000505350.2:c.*8001C>G ENSP00000481752.1:n.*8001C>G
ENST00000507379.6:c.7941C>G ENSP00000423224.2:p.Pro2647=
ENST00000509732.6:c.7995C>G ENSP00000426541.2:p.Pro2665=
ENST00000512211.7:c.7995C>G ENSP00000423828.3:p.Pro2665=
ENST00000257430.9:c.7995C>G MANE Select ENSP00000257430.4:p.Pro2665=
ENST00000257430.8:c.7995C>G ENSP00000257430.4:p.Pro2665=
ENST00000508376.6:c.7995C>G ENSP00000427089.2:p.Pro2665=
ENST00000520401.1:c.231-13060C>G
NM_000038.5:c.7995C>G NP_000029.2:p.Pro2665=
NM_001127510.2:c.7995C>G NP_001120982.1:p.Pro2665=
NM_001127511.2:c.7941C>G NP_001120983.2:p.Pro2647=
NM_001354895.1:c.7995C>G NP_001341824.1:p.Pro2665=
NM_001354896.1:c.8049C>G NP_001341825.1:p.Pro2683=
NM_001354897.1:c.8025C>G NP_001341826.1:p.Pro2675=
NM_001354898.1:c.7920C>G NP_001341827.1:p.Pro2640=
NM_001354899.1:c.7911C>G NP_001341828.1:p.Pro2637=
NM_001354900.1:c.7872C>G NP_001341829.1:p.Pro2624=
NM_001354901.1:c.7818C>G NP_001341830.1:p.Pro2606=
NM_001354902.1:c.7722C>G NP_001341831.1:p.Pro2574=
NM_001354903.1:c.7692C>G NP_001341832.1:p.Pro2564=
NM_001354904.1:c.7617C>G NP_001341833.1:p.Pro2539=
NM_001354905.1:c.7515C>G NP_001341834.1:p.Pro2505=
NM_001354906.1:c.7146C>G NP_001341835.1:p.Pro2382=
NM_000038.6:c.7995C>G MANE Select NP_000029.2:p.Pro2665=
NM_001127510.3:c.7995C>G NP_001120982.1:p.Pro2665=
NM_001127511.3:c.7941C>G NP_001120983.2:p.Pro2647=
NM_001354895.2:c.7995C>G NP_001341824.1:p.Pro2665=
NM_001354896.2:c.8049C>G NP_001341825.1:p.Pro2683=
NM_001354897.2:c.8025C>G NP_001341826.1:p.Pro2675=
NM_001354898.2:c.7920C>G NP_001341827.1:p.Pro2640=
NM_001354899.2:c.7911C>G NP_001341828.1:p.Pro2637=
NM_001354900.2:c.7872C>G NP_001341829.1:p.Pro2624=
NM_001354901.2:c.7818C>G NP_001341830.1:p.Pro2606=
NM_001354902.2:c.7722C>G NP_001341831.1:p.Pro2574=
NM_001354903.2:c.7692C>G NP_001341832.1:p.Pro2564=
NM_001354904.2:c.7617C>G NP_001341833.1:p.Pro2539=
NM_001354905.2:c.7515C>G NP_001341834.1:p.Pro2505=
NM_001354906.2:c.7146C>G NP_001341835.1:p.Pro2382=