Canonical Allele Identifier: CA16028925
Community Standard Title: NM_000038.6(APC):c.3460G>T (p.Glu1154Ter)
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839054G>T , CM000667.2:g.112839054G>T GRCh38
NC_000005.9:g.112174751G>T , CM000667.1:g.112174751G>T GRCh37
NC_000005.8:g.112202650G>T NCBI36
NG_008481.4:g.151534G>T , LRG_130:g.151534G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000038.6:c.3460G>T MANE Select NP_000029.2:p.Glu1154Ter
ENST00000257430.9:c.3460G>T MANE Select ENSP00000257430.4:p.Glu1154Ter
NM_000038.5:c.3460G>T NP_000029.2:p.Glu1154Ter
NM_001127510.2:c.3460G>T NP_001120982.1:p.Glu1154Ter
NM_001127510.3:c.3460G>T NP_001120982.1:p.Glu1154Ter
NM_001127511.2:c.3406G>T NP_001120983.2:p.Glu1136Ter
NM_001127511.3:c.3406G>T NP_001120983.2:p.Glu1136Ter
NM_001354895.1:c.3460G>T NP_001341824.1:p.Glu1154Ter
NM_001354895.2:c.3460G>T NP_001341824.1:p.Glu1154Ter
NM_001354896.1:c.3514G>T NP_001341825.1:p.Glu1172Ter
NM_001354896.2:c.3514G>T NP_001341825.1:p.Glu1172Ter
NM_001354897.1:c.3490G>T NP_001341826.1:p.Glu1164Ter
NM_001354897.2:c.3490G>T NP_001341826.1:p.Glu1164Ter
NM_001354898.1:c.3385G>T NP_001341827.1:p.Glu1129Ter
NM_001354898.2:c.3385G>T NP_001341827.1:p.Glu1129Ter
NM_001354899.1:c.3376G>T NP_001341828.1:p.Glu1126Ter
NM_001354899.2:c.3376G>T NP_001341828.1:p.Glu1126Ter
NM_001354900.1:c.3337G>T NP_001341829.1:p.Glu1113Ter
NM_001354900.2:c.3337G>T NP_001341829.1:p.Glu1113Ter
NM_001354901.1:c.3283G>T NP_001341830.1:p.Glu1095Ter
NM_001354901.2:c.3283G>T NP_001341830.1:p.Glu1095Ter
NM_001354902.1:c.3187G>T NP_001341831.1:p.Glu1063Ter
NM_001354902.2:c.3187G>T NP_001341831.1:p.Glu1063Ter
NM_001354903.1:c.3157G>T NP_001341832.1:p.Glu1053Ter
NM_001354903.2:c.3157G>T NP_001341832.1:p.Glu1053Ter
NM_001354904.1:c.3082G>T NP_001341833.1:p.Glu1028Ter
NM_001354904.2:c.3082G>T NP_001341833.1:p.Glu1028Ter
NM_001354905.1:c.2980G>T NP_001341834.1:p.Glu994Ter
NM_001354905.2:c.2980G>T NP_001341834.1:p.Glu994Ter
NM_001354906.1:c.2611G>T NP_001341835.1:p.Glu871Ter
NM_001354906.2:c.2611G>T NP_001341835.1:p.Glu871Ter
ENST00000257430.8:c.3460G>T ENSP00000257430.4:p.Glu1154Ter
ENST00000502371.2:c.1813G>T
ENST00000502371.3:c.3125G>T ENSP00000484935.2:n.3125G>T
ENST00000504915.3:c.3514G>T ENSP00000473355.2:p.Glu1172Ter
ENST00000505350.2:c.*3466G>T ENSP00000481752.1:n.*3466G>T
ENST00000507379.5:c.3406G>T
ENST00000507379.6:c.3406G>T ENSP00000423224.2:p.Glu1136Ter
ENST00000508376.6:c.3460G>T ENSP00000427089.2:p.Glu1154Ter
ENST00000508624.5:c.*2782G>T ENSP00000424265.1:n.*2782G>T
ENST00000509732.6:c.3460G>T ENSP00000426541.2:p.Glu1154Ter
ENST00000512211.6:c.3460G>T ENSP00000423828.2:p.Glu1154Ter
ENST00000512211.7:c.3460G>T ENSP00000423828.3:p.Glu1154Ter
ENST00000520401.1:c.230+10082G>T