Canonical Allele Identifier: CA16028639
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838926A>G , CM000667.2:g.112838926A>G GRCh38
NC_000005.9:g.112174623A>G , CM000667.1:g.112174623A>G GRCh37
NC_000005.8:g.112202522A>G NCBI36
NG_008481.4:g.151406A>G , LRG_130:g.151406A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.2997A>G ENSP00000484935.2:n.2997A>G
ENST00000504915.3:c.3386A>G ENSP00000473355.2:p.Glu1129Gly
ENST00000505350.2:c.*3338A>G ENSP00000481752.1:n.*3338A>G
ENST00000507379.6:c.3278A>G ENSP00000423224.2:p.Glu1093Gly
ENST00000509732.6:c.3332A>G ENSP00000426541.2:p.Glu1111Gly
ENST00000512211.7:c.3332A>G ENSP00000423828.3:p.Glu1111Gly
ENST00000257430.9:c.3332A>G MANE Select ENSP00000257430.4:p.Glu1111Gly
ENST00000257430.8:c.3332A>G ENSP00000257430.4:p.Glu1111Gly
ENST00000502371.2:c.1685A>G
ENST00000507379.5:c.3278A>G ENSP00000423224.1:p.Glu1093Gly
ENST00000508376.6:c.3332A>G ENSP00000427089.2:p.Glu1111Gly
ENST00000508624.5:c.*2654A>G ENSP00000424265.1:n.*2654A>G
ENST00000512211.6:c.3332A>G ENSP00000423828.2:p.Glu1111Gly
ENST00000520401.1:c.230+9954A>G
NM_000038.5:c.3332A>G NP_000029.2:p.Glu1111Gly
NM_001127510.2:c.3332A>G NP_001120982.1:p.Glu1111Gly
NM_001127511.2:c.3278A>G NP_001120983.2:p.Glu1093Gly
NM_001354895.1:c.3332A>G NP_001341824.1:p.Glu1111Gly
NM_001354896.1:c.3386A>G NP_001341825.1:p.Glu1129Gly
NM_001354897.1:c.3362A>G NP_001341826.1:p.Glu1121Gly
NM_001354898.1:c.3257A>G NP_001341827.1:p.Glu1086Gly
NM_001354899.1:c.3248A>G NP_001341828.1:p.Glu1083Gly
NM_001354900.1:c.3209A>G NP_001341829.1:p.Glu1070Gly
NM_001354901.1:c.3155A>G NP_001341830.1:p.Glu1052Gly
NM_001354902.1:c.3059A>G NP_001341831.1:p.Glu1020Gly
NM_001354903.1:c.3029A>G NP_001341832.1:p.Glu1010Gly
NM_001354904.1:c.2954A>G NP_001341833.1:p.Glu985Gly
NM_001354905.1:c.2852A>G NP_001341834.1:p.Glu951Gly
NM_001354906.1:c.2483A>G NP_001341835.1:p.Glu828Gly
NM_000038.6:c.3332A>G MANE Select NP_000029.2:p.Glu1111Gly
NM_001127510.3:c.3332A>G NP_001120982.1:p.Glu1111Gly
NM_001127511.3:c.3278A>G NP_001120983.2:p.Glu1093Gly
NM_001354895.2:c.3332A>G NP_001341824.1:p.Glu1111Gly
NM_001354896.2:c.3386A>G NP_001341825.1:p.Glu1129Gly
NM_001354897.2:c.3362A>G NP_001341826.1:p.Glu1121Gly
NM_001354898.2:c.3257A>G NP_001341827.1:p.Glu1086Gly
NM_001354899.2:c.3248A>G NP_001341828.1:p.Glu1083Gly
NM_001354900.2:c.3209A>G NP_001341829.1:p.Glu1070Gly
NM_001354901.2:c.3155A>G NP_001341830.1:p.Glu1052Gly
NM_001354902.2:c.3059A>G NP_001341831.1:p.Glu1020Gly
NM_001354903.2:c.3029A>G NP_001341832.1:p.Glu1010Gly
NM_001354904.2:c.2954A>G NP_001341833.1:p.Glu985Gly
NM_001354905.2:c.2852A>G NP_001341834.1:p.Glu951Gly
NM_001354906.2:c.2483A>G NP_001341835.1:p.Glu828Gly