Canonical Allele Identifier: CA1573487867
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838956T= , CM000667.2:g.112838956T= GRCh38
NC_000005.9:g.112174653T= , CM000667.1:g.112174653T= GRCh37
NC_000005.8:g.112202552T= NCBI36
NG_008481.4:g.151436T= , LRG_130:g.151436T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.3027T= ENSP00000484935.2:n.3027T=
ENST00000504915.3:c.3416T= ENSP00000473355.2:p.Ile1139=
ENST00000505350.2:c.*3368T= ENSP00000481752.1:n.*3368T=
ENST00000507379.6:c.3308T= ENSP00000423224.2:p.Ile1103=
ENST00000509732.6:c.3362T= ENSP00000426541.2:p.Ile1121=
ENST00000512211.7:c.3362T= ENSP00000423828.3:p.Ile1121=
ENST00000257430.9:c.3362T= MANE Select ENSP00000257430.4:p.Ile1121=
ENST00000257430.8:c.3362T= ENSP00000257430.4:p.Ile1121=
ENST00000502371.2:c.1715T=
ENST00000507379.5:c.3308T= ENSP00000423224.1:p.Ile1103=
ENST00000508376.6:c.3362T= ENSP00000427089.2:p.Ile1121=
ENST00000508624.5:c.*2684T= ENSP00000424265.1:n.*2684T=
ENST00000512211.6:c.3362T= ENSP00000423828.2:p.Ile1121=
ENST00000520401.1:c.230+9984T=
NM_000038.5:c.3362T= NP_000029.2:p.Ile1121=
NM_001127510.2:c.3362T= NP_001120982.1:p.Ile1121=
NM_001127511.2:c.3308T= NP_001120983.2:p.Ile1103=
NM_001354895.1:c.3362T= NP_001341824.1:p.Ile1121=
NM_001354896.1:c.3416T= NP_001341825.1:p.Ile1139=
NM_001354897.1:c.3392T= NP_001341826.1:p.Ile1131=
NM_001354898.1:c.3287T= NP_001341827.1:p.Ile1096=
NM_001354899.1:c.3278T= NP_001341828.1:p.Ile1093=
NM_001354900.1:c.3239T= NP_001341829.1:p.Ile1080=
NM_001354901.1:c.3185T= NP_001341830.1:p.Ile1062=
NM_001354902.1:c.3089T= NP_001341831.1:p.Ile1030=
NM_001354903.1:c.3059T= NP_001341832.1:p.Ile1020=
NM_001354904.1:c.2984T= NP_001341833.1:p.Ile995=
NM_001354905.1:c.2882T= NP_001341834.1:p.Ile961=
NM_001354906.1:c.2513T= NP_001341835.1:p.Ile838=
NM_000038.6:c.3362T= MANE Select NP_000029.2:p.Ile1121=
NM_001127510.3:c.3362T= NP_001120982.1:p.Ile1121=
NM_001127511.3:c.3308T= NP_001120983.2:p.Ile1103=
NM_001354895.2:c.3362T= NP_001341824.1:p.Ile1121=
NM_001354896.2:c.3416T= NP_001341825.1:p.Ile1139=
NM_001354897.2:c.3392T= NP_001341826.1:p.Ile1131=
NM_001354898.2:c.3287T= NP_001341827.1:p.Ile1096=
NM_001354899.2:c.3278T= NP_001341828.1:p.Ile1093=
NM_001354900.2:c.3239T= NP_001341829.1:p.Ile1080=
NM_001354901.2:c.3185T= NP_001341830.1:p.Ile1062=
NM_001354902.2:c.3089T= NP_001341831.1:p.Ile1030=
NM_001354903.2:c.3059T= NP_001341832.1:p.Ile1020=
NM_001354904.2:c.2984T= NP_001341833.1:p.Ile995=
NM_001354905.2:c.2882T= NP_001341834.1:p.Ile961=
NM_001354906.2:c.2513T= NP_001341835.1:p.Ile838=