Canonical Allele Identifier: CA1573473388
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840632C= , CM000667.2:g.112840632C= GRCh38
NC_000005.9:g.112176329C= , CM000667.1:g.112176329C= GRCh37
NC_000005.8:g.112204228C= NCBI36
NG_008481.4:g.153112C= , LRG_130:g.153112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5092C= ENSP00000473355.2:p.Gln1698=
ENST00000505350.2:c.*5044C= ENSP00000481752.1:n.*5044C=
ENST00000507379.6:c.4984C= ENSP00000423224.2:p.Gln1662=
ENST00000509732.6:c.5038C= ENSP00000426541.2:p.Gln1680=
ENST00000512211.7:c.5038C= ENSP00000423828.3:p.Gln1680=
ENST00000257430.9:c.5038C= MANE Select ENSP00000257430.4:p.Gln1680=
ENST00000257430.8:c.5038C= ENSP00000257430.4:p.Gln1680=
ENST00000508376.6:c.5038C= ENSP00000427089.2:p.Gln1680=
ENST00000508624.5:c.*4360C= ENSP00000424265.1:n.*4360C=
ENST00000520401.1:c.230+11660C=
NM_000038.5:c.5038C= NP_000029.2:p.Gln1680=
NM_001127510.2:c.5038C= NP_001120982.1:p.Gln1680=
NM_001127511.2:c.4984C= NP_001120983.2:p.Gln1662=
NM_001354895.1:c.5038C= NP_001341824.1:p.Gln1680=
NM_001354896.1:c.5092C= NP_001341825.1:p.Gln1698=
NM_001354897.1:c.5068C= NP_001341826.1:p.Gln1690=
NM_001354898.1:c.4963C= NP_001341827.1:p.Gln1655=
NM_001354899.1:c.4954C= NP_001341828.1:p.Gln1652=
NM_001354900.1:c.4915C= NP_001341829.1:p.Gln1639=
NM_001354901.1:c.4861C= NP_001341830.1:p.Gln1621=
NM_001354902.1:c.4765C= NP_001341831.1:p.Gln1589=
NM_001354903.1:c.4735C= NP_001341832.1:p.Gln1579=
NM_001354904.1:c.4660C= NP_001341833.1:p.Gln1554=
NM_001354905.1:c.4558C= NP_001341834.1:p.Gln1520=
NM_001354906.1:c.4189C= NP_001341835.1:p.Gln1397=
NM_000038.6:c.5038C= MANE Select NP_000029.2:p.Gln1680=
NM_001127510.3:c.5038C= NP_001120982.1:p.Gln1680=
NM_001127511.3:c.4984C= NP_001120983.2:p.Gln1662=
NM_001354895.2:c.5038C= NP_001341824.1:p.Gln1680=
NM_001354896.2:c.5092C= NP_001341825.1:p.Gln1698=
NM_001354897.2:c.5068C= NP_001341826.1:p.Gln1690=
NM_001354898.2:c.4963C= NP_001341827.1:p.Gln1655=
NM_001354899.2:c.4954C= NP_001341828.1:p.Gln1652=
NM_001354900.2:c.4915C= NP_001341829.1:p.Gln1639=
NM_001354901.2:c.4861C= NP_001341830.1:p.Gln1621=
NM_001354902.2:c.4765C= NP_001341831.1:p.Gln1589=
NM_001354903.2:c.4735C= NP_001341832.1:p.Gln1579=
NM_001354904.2:c.4660C= NP_001341833.1:p.Gln1554=
NM_001354905.2:c.4558C= NP_001341834.1:p.Gln1520=
NM_001354906.2:c.4189C= NP_001341835.1:p.Gln1397=