Canonical Allele Identifier: CA1573470409
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840239_112840240delinsCA , CM000667.2:g.112840239_112840240delinsCA GRCh38
NC_000005.9:g.112175936_112175937delinsCA , CM000667.1:g.112175936_112175937delinsCA GRCh37
NC_000005.8:g.112203835_112203836delinsCA NCBI36
NG_008481.4:g.152719_152720delinsCA , LRG_130:g.152719_152720delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4699_4700delinsCA ENSP00000473355.2:p.Gln1567=
ENST00000505350.2:c.*4651_*4652delinsCA ENSP00000481752.1:n.*4651_*4652delinsCA
ENST00000507379.6:c.4591_4592delinsCA ENSP00000423224.2:p.Gln1531=
ENST00000509732.6:c.4645_4646delinsCA ENSP00000426541.2:p.Gln1549=
ENST00000512211.7:c.4645_4646delinsCA ENSP00000423828.3:p.Gln1549=
ENST00000257430.9:c.4645_4646delinsCA MANE Select ENSP00000257430.4:p.Gln1549=
ENST00000257430.8:c.4645_4646delinsCA ENSP00000257430.4:p.Gln1549=
ENST00000508376.6:c.4645_4646delinsCA ENSP00000427089.2:p.Gln1549=
ENST00000508624.5:c.*3967_*3968delinsCA ENSP00000424265.1:n.*3967_*3968delinsCA
ENST00000520401.1:c.230+11267_230+11268delinsCA
NM_000038.5:c.4645_4646delinsCA NP_000029.2:p.Gln1549=
NM_001127510.2:c.4645_4646delinsCA NP_001120982.1:p.Gln1549=
NM_001127511.2:c.4591_4592delinsCA NP_001120983.2:p.Gln1531=
NM_001354895.1:c.4645_4646delinsCA NP_001341824.1:p.Gln1549=
NM_001354896.1:c.4699_4700delinsCA NP_001341825.1:p.Gln1567=
NM_001354897.1:c.4675_4676delinsCA NP_001341826.1:p.Gln1559=
NM_001354898.1:c.4570_4571delinsCA NP_001341827.1:p.Gln1524=
NM_001354899.1:c.4561_4562delinsCA NP_001341828.1:p.Gln1521=
NM_001354900.1:c.4522_4523delinsCA NP_001341829.1:p.Gln1508=
NM_001354901.1:c.4468_4469delinsCA NP_001341830.1:p.Gln1490=
NM_001354902.1:c.4372_4373delinsCA NP_001341831.1:p.Gln1458=
NM_001354903.1:c.4342_4343delinsCA NP_001341832.1:p.Gln1448=
NM_001354904.1:c.4267_4268delinsCA NP_001341833.1:p.Gln1423=
NM_001354905.1:c.4165_4166delinsCA NP_001341834.1:p.Gln1389=
NM_001354906.1:c.3796_3797delinsCA NP_001341835.1:p.Gln1266=
NM_000038.6:c.4645_4646delinsCA MANE Select NP_000029.2:p.Gln1549=
NM_001127510.3:c.4645_4646delinsCA NP_001120982.1:p.Gln1549=
NM_001127511.3:c.4591_4592delinsCA NP_001120983.2:p.Gln1531=
NM_001354895.2:c.4645_4646delinsCA NP_001341824.1:p.Gln1549=
NM_001354896.2:c.4699_4700delinsCA NP_001341825.1:p.Gln1567=
NM_001354897.2:c.4675_4676delinsCA NP_001341826.1:p.Gln1559=
NM_001354898.2:c.4570_4571delinsCA NP_001341827.1:p.Gln1524=
NM_001354899.2:c.4561_4562delinsCA NP_001341828.1:p.Gln1521=
NM_001354900.2:c.4522_4523delinsCA NP_001341829.1:p.Gln1508=
NM_001354901.2:c.4468_4469delinsCA NP_001341830.1:p.Gln1490=
NM_001354902.2:c.4372_4373delinsCA NP_001341831.1:p.Gln1458=
NM_001354903.2:c.4342_4343delinsCA NP_001341832.1:p.Gln1448=
NM_001354904.2:c.4267_4268delinsCA NP_001341833.1:p.Gln1423=
NM_001354905.2:c.4165_4166delinsCA NP_001341834.1:p.Gln1389=
NM_001354906.2:c.3796_3797delinsCA NP_001341835.1:p.Gln1266=