Canonical Allele Identifier: CA1573476327
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843732_112843734delinsTGC , CM000667.2:g.112843732_112843734delinsTGC GRCh38
NC_000005.9:g.112179429_112179431delinsTGC , CM000667.1:g.112179429_112179431delinsTGC GRCh37
NC_000005.8:g.112207328_112207330delinsTGC NCBI36
NG_008481.4:g.156212_156214delinsTGC , LRG_130:g.156212_156214delinsTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8192_8194delinsTGC ENSP00000473355.2:p.Met2731=
ENST00000505350.2:c.*8144_*8146delinsTGC ENSP00000481752.1:n.*8144_*8146delinsTGC
ENST00000507379.6:c.8084_8086delinsTGC ENSP00000423224.2:p.Met2695=
ENST00000509732.6:c.8138_8140delinsTGC ENSP00000426541.2:p.Met2713=
ENST00000512211.7:c.8138_8140delinsTGC ENSP00000423828.3:p.Met2713=
ENST00000257430.9:c.8138_8140delinsTGC MANE Select ENSP00000257430.4:p.Met2713=
ENST00000257430.8:c.8138_8140delinsTGC ENSP00000257430.4:p.Met2713=
ENST00000508376.6:c.8138_8140delinsTGC ENSP00000427089.2:p.Met2713=
ENST00000520401.1:c.231-12917_231-12915delinsTGC
NM_000038.5:c.8138_8140delinsTGC NP_000029.2:p.Met2713=
NM_001127510.2:c.8138_8140delinsTGC NP_001120982.1:p.Met2713=
NM_001127511.2:c.8084_8086delinsTGC NP_001120983.2:p.Met2695=
NM_001354895.1:c.8138_8140delinsTGC NP_001341824.1:p.Met2713=
NM_001354896.1:c.8192_8194delinsTGC NP_001341825.1:p.Met2731=
NM_001354897.1:c.8168_8170delinsTGC NP_001341826.1:p.Met2723=
NM_001354898.1:c.8063_8065delinsTGC NP_001341827.1:p.Met2688=
NM_001354899.1:c.8054_8056delinsTGC NP_001341828.1:p.Met2685=
NM_001354900.1:c.8015_8017delinsTGC NP_001341829.1:p.Met2672=
NM_001354901.1:c.7961_7963delinsTGC NP_001341830.1:p.Met2654=
NM_001354902.1:c.7865_7867delinsTGC NP_001341831.1:p.Met2622=
NM_001354903.1:c.7835_7837delinsTGC NP_001341832.1:p.Met2612=
NM_001354904.1:c.7760_7762delinsTGC NP_001341833.1:p.Met2587=
NM_001354905.1:c.7658_7660delinsTGC NP_001341834.1:p.Met2553=
NM_001354906.1:c.7289_7291delinsTGC NP_001341835.1:p.Met2430=
NM_000038.6:c.8138_8140delinsTGC MANE Select NP_000029.2:p.Met2713=
NM_001127510.3:c.8138_8140delinsTGC NP_001120982.1:p.Met2713=
NM_001127511.3:c.8084_8086delinsTGC NP_001120983.2:p.Met2695=
NM_001354895.2:c.8138_8140delinsTGC NP_001341824.1:p.Met2713=
NM_001354896.2:c.8192_8194delinsTGC NP_001341825.1:p.Met2731=
NM_001354897.2:c.8168_8170delinsTGC NP_001341826.1:p.Met2723=
NM_001354898.2:c.8063_8065delinsTGC NP_001341827.1:p.Met2688=
NM_001354899.2:c.8054_8056delinsTGC NP_001341828.1:p.Met2685=
NM_001354900.2:c.8015_8017delinsTGC NP_001341829.1:p.Met2672=
NM_001354901.2:c.7961_7963delinsTGC NP_001341830.1:p.Met2654=
NM_001354902.2:c.7865_7867delinsTGC NP_001341831.1:p.Met2622=
NM_001354903.2:c.7835_7837delinsTGC NP_001341832.1:p.Met2612=
NM_001354904.2:c.7760_7762delinsTGC NP_001341833.1:p.Met2587=
NM_001354905.2:c.7658_7660delinsTGC NP_001341834.1:p.Met2553=
NM_001354906.2:c.7289_7291delinsTGC NP_001341835.1:p.Met2430=