Canonical Allele Identifier: CA1573475199
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843571G= , CM000667.2:g.112843571G= GRCh38
NC_000005.9:g.112179268G= , CM000667.1:g.112179268G= GRCh37
NC_000005.8:g.112207167G= NCBI36
NG_008481.4:g.156051G= , LRG_130:g.156051G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8031G= ENSP00000473355.2:p.Val2677=
ENST00000505350.2:c.*7983G= ENSP00000481752.1:n.*7983G=
ENST00000507379.6:c.7923G= ENSP00000423224.2:p.Val2641=
ENST00000509732.6:c.7977G= ENSP00000426541.2:p.Val2659=
ENST00000512211.7:c.7977G= ENSP00000423828.3:p.Val2659=
ENST00000257430.9:c.7977G= MANE Select ENSP00000257430.4:p.Val2659=
ENST00000257430.8:c.7977G= ENSP00000257430.4:p.Val2659=
ENST00000508376.6:c.7977G= ENSP00000427089.2:p.Val2659=
ENST00000520401.1:c.231-13078G=
NM_000038.5:c.7977G= NP_000029.2:p.Val2659=
NM_001127510.2:c.7977G= NP_001120982.1:p.Val2659=
NM_001127511.2:c.7923G= NP_001120983.2:p.Val2641=
NM_001354895.1:c.7977G= NP_001341824.1:p.Val2659=
NM_001354896.1:c.8031G= NP_001341825.1:p.Val2677=
NM_001354897.1:c.8007G= NP_001341826.1:p.Val2669=
NM_001354898.1:c.7902G= NP_001341827.1:p.Val2634=
NM_001354899.1:c.7893G= NP_001341828.1:p.Val2631=
NM_001354900.1:c.7854G= NP_001341829.1:p.Val2618=
NM_001354901.1:c.7800G= NP_001341830.1:p.Val2600=
NM_001354902.1:c.7704G= NP_001341831.1:p.Val2568=
NM_001354903.1:c.7674G= NP_001341832.1:p.Val2558=
NM_001354904.1:c.7599G= NP_001341833.1:p.Val2533=
NM_001354905.1:c.7497G= NP_001341834.1:p.Val2499=
NM_001354906.1:c.7128G= NP_001341835.1:p.Val2376=
NM_000038.6:c.7977G= MANE Select NP_000029.2:p.Val2659=
NM_001127510.3:c.7977G= NP_001120982.1:p.Val2659=
NM_001127511.3:c.7923G= NP_001120983.2:p.Val2641=
NM_001354895.2:c.7977G= NP_001341824.1:p.Val2659=
NM_001354896.2:c.8031G= NP_001341825.1:p.Val2677=
NM_001354897.2:c.8007G= NP_001341826.1:p.Val2669=
NM_001354898.2:c.7902G= NP_001341827.1:p.Val2634=
NM_001354899.2:c.7893G= NP_001341828.1:p.Val2631=
NM_001354900.2:c.7854G= NP_001341829.1:p.Val2618=
NM_001354901.2:c.7800G= NP_001341830.1:p.Val2600=
NM_001354902.2:c.7704G= NP_001341831.1:p.Val2568=
NM_001354903.2:c.7674G= NP_001341832.1:p.Val2558=
NM_001354904.2:c.7599G= NP_001341833.1:p.Val2533=
NM_001354905.2:c.7497G= NP_001341834.1:p.Val2499=
NM_001354906.2:c.7128G= NP_001341835.1:p.Val2376=