Canonical Allele Identifier: CA16028764
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838986A>G , CM000667.2:g.112838986A>G GRCh38
NC_000005.9:g.112174683A>G , CM000667.1:g.112174683A>G GRCh37
NC_000005.8:g.112202582A>G NCBI36
NG_008481.4:g.151466A>G , LRG_130:g.151466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.3057A>G ENSP00000484935.2:n.3057A>G
ENST00000504915.3:c.3446A>G ENSP00000473355.2:p.Gln1149Arg
ENST00000505350.2:c.*3398A>G ENSP00000481752.1:n.*3398A>G
ENST00000507379.6:c.3338A>G ENSP00000423224.2:p.Gln1113Arg
ENST00000509732.6:c.3392A>G ENSP00000426541.2:p.Gln1131Arg
ENST00000512211.7:c.3392A>G ENSP00000423828.3:p.Gln1131Arg
ENST00000257430.9:c.3392A>G MANE Select ENSP00000257430.4:p.Gln1131Arg
ENST00000257430.8:c.3392A>G ENSP00000257430.4:p.Gln1131Arg
ENST00000502371.2:c.1745A>G
ENST00000507379.5:c.3338A>G ENSP00000423224.1:p.Gln1113Arg
ENST00000508376.6:c.3392A>G ENSP00000427089.2:p.Gln1131Arg
ENST00000508624.5:c.*2714A>G ENSP00000424265.1:n.*2714A>G
ENST00000512211.6:c.3392A>G ENSP00000423828.2:p.Gln1131Arg
ENST00000520401.1:c.230+10014A>G
NM_000038.5:c.3392A>G NP_000029.2:p.Gln1131Arg
NM_001127510.2:c.3392A>G NP_001120982.1:p.Gln1131Arg
NM_001127511.2:c.3338A>G NP_001120983.2:p.Gln1113Arg
NM_001354895.1:c.3392A>G NP_001341824.1:p.Gln1131Arg
NM_001354896.1:c.3446A>G NP_001341825.1:p.Gln1149Arg
NM_001354897.1:c.3422A>G NP_001341826.1:p.Gln1141Arg
NM_001354898.1:c.3317A>G NP_001341827.1:p.Gln1106Arg
NM_001354899.1:c.3308A>G NP_001341828.1:p.Gln1103Arg
NM_001354900.1:c.3269A>G NP_001341829.1:p.Gln1090Arg
NM_001354901.1:c.3215A>G NP_001341830.1:p.Gln1072Arg
NM_001354902.1:c.3119A>G NP_001341831.1:p.Gln1040Arg
NM_001354903.1:c.3089A>G NP_001341832.1:p.Gln1030Arg
NM_001354904.1:c.3014A>G NP_001341833.1:p.Gln1005Arg
NM_001354905.1:c.2912A>G NP_001341834.1:p.Gln971Arg
NM_001354906.1:c.2543A>G NP_001341835.1:p.Gln848Arg
NM_000038.6:c.3392A>G MANE Select NP_000029.2:p.Gln1131Arg
NM_001127510.3:c.3392A>G NP_001120982.1:p.Gln1131Arg
NM_001127511.3:c.3338A>G NP_001120983.2:p.Gln1113Arg
NM_001354895.2:c.3392A>G NP_001341824.1:p.Gln1131Arg
NM_001354896.2:c.3446A>G NP_001341825.1:p.Gln1149Arg
NM_001354897.2:c.3422A>G NP_001341826.1:p.Gln1141Arg
NM_001354898.2:c.3317A>G NP_001341827.1:p.Gln1106Arg
NM_001354899.2:c.3308A>G NP_001341828.1:p.Gln1103Arg
NM_001354900.2:c.3269A>G NP_001341829.1:p.Gln1090Arg
NM_001354901.2:c.3215A>G NP_001341830.1:p.Gln1072Arg
NM_001354902.2:c.3119A>G NP_001341831.1:p.Gln1040Arg
NM_001354903.2:c.3089A>G NP_001341832.1:p.Gln1030Arg
NM_001354904.2:c.3014A>G NP_001341833.1:p.Gln1005Arg
NM_001354905.2:c.2912A>G NP_001341834.1:p.Gln971Arg
NM_001354906.2:c.2543A>G NP_001341835.1:p.Gln848Arg