Canonical Allele Identifier: CA1573471748
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112835169_112835170delinsTA , CM000667.2:g.112835169_112835170delinsTA GRCh38
NC_000005.9:g.112170866_112170867delinsTA , CM000667.1:g.112170866_112170867delinsTA GRCh37
NC_000005.8:g.112198765_112198766delinsTA NCBI36
NG_008481.4:g.147649_147650delinsTA , LRG_130:g.147649_147650delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.1623+4_1623+5delinsTA ENSP00000484935.2:n.1623+4_1623+5delinsTA
ENST00000504915.3:c.2012+4_2012+5delinsTA ENSP00000473355.2:n.2012+4_2012+5delinsTA
ENST00000505350.2:c.*1964+4_*1964+5delinsTA ENSP00000481752.1:n.*1964+4_*1964+5delinsTA
ENST00000507379.6:c.1904+4_1904+5delinsTA ENSP00000423224.2:n.1904+4_1904+5delinsTA
ENST00000509732.6:c.1958+4_1958+5delinsTA ENSP00000426541.2:n.1958+4_1958+5delinsTA
ENST00000512211.7:c.1958+4_1958+5delinsTA ENSP00000423828.3:n.1958+4_1958+5delinsTA
ENST00000257430.9:c.1958+4_1958+5delinsTA MANE Select ENSP00000257430.4:n.1958+4_1958+5delinsTA
ENST00000257430.8:c.1958+4_1958+5delinsTA ENSP00000257430.4:n.1958+4_1958+5delinsTA
ENST00000502371.2:c.311+4_311+5delinsTA
ENST00000504915.2:c.647+4_647+5delinsTA ENSP00000473355.1:n.647+4_647+5delinsTA
ENST00000507379.5:c.1904+4_1904+5delinsTA ENSP00000423224.1:n.1904+4_1904+5delinsTA
ENST00000508376.6:c.1958+4_1958+5delinsTA ENSP00000427089.2:n.1958+4_1958+5delinsTA
ENST00000508624.5:c.*1280+4_*1280+5delinsTA ENSP00000424265.1:n.*1280+4_*1280+5delinsTA
ENST00000512211.6:c.1958+4_1958+5delinsTA ENSP00000423828.2:n.1958+4_1958+5delinsTA
ENST00000520401.1:c.230+6197_230+6198delinsTA
NM_000038.5:c.1958+4_1958+5delinsTA NP_000029.2:n.1958+4_1958+5delinsTA
NM_001127510.2:c.1958+4_1958+5delinsTA NP_001120982.1:n.1958+4_1958+5delinsTA
NM_001127511.2:c.1904+4_1904+5delinsTA NP_001120983.2:n.1904+4_1904+5delinsTA
NM_001354895.1:c.1958+4_1958+5delinsTA NP_001341824.1:n.1958+4_1958+5delinsTA
NM_001354896.1:c.2012+4_2012+5delinsTA NP_001341825.1:n.2012+4_2012+5delinsTA
NM_001354897.1:c.1988+4_1988+5delinsTA NP_001341826.1:n.1988+4_1988+5delinsTA
NM_001354898.1:c.1883+4_1883+5delinsTA NP_001341827.1:n.1883+4_1883+5delinsTA
NM_001354899.1:c.1874+4_1874+5delinsTA NP_001341828.1:n.1874+4_1874+5delinsTA
NM_001354900.1:c.1835+4_1835+5delinsTA NP_001341829.1:n.1835+4_1835+5delinsTA
NM_001354901.1:c.1781+4_1781+5delinsTA NP_001341830.1:n.1781+4_1781+5delinsTA
NM_001354902.1:c.1685+4_1685+5delinsTA NP_001341831.1:n.1685+4_1685+5delinsTA
NM_001354903.1:c.1655+4_1655+5delinsTA NP_001341832.1:n.1655+4_1655+5delinsTA
NM_001354904.1:c.1580+4_1580+5delinsTA NP_001341833.1:n.1580+4_1580+5delinsTA
NM_001354905.1:c.1478+4_1478+5delinsTA NP_001341834.1:n.1478+4_1478+5delinsTA
NM_001354906.1:c.1109+4_1109+5delinsTA NP_001341835.1:n.1109+4_1109+5delinsTA
NM_000038.6:c.1958+4_1958+5delinsTA MANE Select NP_000029.2:n.1958+4_1958+5delinsTA
NM_001127510.3:c.1958+4_1958+5delinsTA NP_001120982.1:n.1958+4_1958+5delinsTA
NM_001127511.3:c.1904+4_1904+5delinsTA NP_001120983.2:n.1904+4_1904+5delinsTA
NM_001354895.2:c.1958+4_1958+5delinsTA NP_001341824.1:n.1958+4_1958+5delinsTA
NM_001354896.2:c.2012+4_2012+5delinsTA NP_001341825.1:n.2012+4_2012+5delinsTA
NM_001354897.2:c.1988+4_1988+5delinsTA NP_001341826.1:n.1988+4_1988+5delinsTA
NM_001354898.2:c.1883+4_1883+5delinsTA NP_001341827.1:n.1883+4_1883+5delinsTA
NM_001354899.2:c.1874+4_1874+5delinsTA NP_001341828.1:n.1874+4_1874+5delinsTA
NM_001354900.2:c.1835+4_1835+5delinsTA NP_001341829.1:n.1835+4_1835+5delinsTA
NM_001354901.2:c.1781+4_1781+5delinsTA NP_001341830.1:n.1781+4_1781+5delinsTA
NM_001354902.2:c.1685+4_1685+5delinsTA NP_001341831.1:n.1685+4_1685+5delinsTA
NM_001354903.2:c.1655+4_1655+5delinsTA NP_001341832.1:n.1655+4_1655+5delinsTA
NM_001354904.2:c.1580+4_1580+5delinsTA NP_001341833.1:n.1580+4_1580+5delinsTA
NM_001354905.2:c.1478+4_1478+5delinsTA NP_001341834.1:n.1478+4_1478+5delinsTA
NM_001354906.2:c.1109+4_1109+5delinsTA NP_001341835.1:n.1109+4_1109+5delinsTA