Canonical Allele Identifier: CA1573472952
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840588C= , CM000667.2:g.112840588C= GRCh38
NC_000005.9:g.112176285C= , CM000667.1:g.112176285C= GRCh37
NC_000005.8:g.112204184C= NCBI36
NG_008481.4:g.153068C= , LRG_130:g.153068C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5048C= ENSP00000473355.2:p.Pro1683=
ENST00000505350.2:c.*5000C= ENSP00000481752.1:n.*5000C=
ENST00000507379.6:c.4940C= ENSP00000423224.2:p.Pro1647=
ENST00000509732.6:c.4994C= ENSP00000426541.2:p.Pro1665=
ENST00000512211.7:c.4994C= ENSP00000423828.3:p.Pro1665=
ENST00000257430.9:c.4994C= MANE Select ENSP00000257430.4:p.Pro1665=
ENST00000257430.8:c.4994C= ENSP00000257430.4:p.Pro1665=
ENST00000508376.6:c.4994C= ENSP00000427089.2:p.Pro1665=
ENST00000508624.5:c.*4316C= ENSP00000424265.1:n.*4316C=
ENST00000520401.1:c.230+11616C=
NM_000038.5:c.4994C= NP_000029.2:p.Pro1665=
NM_001127510.2:c.4994C= NP_001120982.1:p.Pro1665=
NM_001127511.2:c.4940C= NP_001120983.2:p.Pro1647=
NM_001354895.1:c.4994C= NP_001341824.1:p.Pro1665=
NM_001354896.1:c.5048C= NP_001341825.1:p.Pro1683=
NM_001354897.1:c.5024C= NP_001341826.1:p.Pro1675=
NM_001354898.1:c.4919C= NP_001341827.1:p.Pro1640=
NM_001354899.1:c.4910C= NP_001341828.1:p.Pro1637=
NM_001354900.1:c.4871C= NP_001341829.1:p.Pro1624=
NM_001354901.1:c.4817C= NP_001341830.1:p.Pro1606=
NM_001354902.1:c.4721C= NP_001341831.1:p.Pro1574=
NM_001354903.1:c.4691C= NP_001341832.1:p.Pro1564=
NM_001354904.1:c.4616C= NP_001341833.1:p.Pro1539=
NM_001354905.1:c.4514C= NP_001341834.1:p.Pro1505=
NM_001354906.1:c.4145C= NP_001341835.1:p.Pro1382=
NM_000038.6:c.4994C= MANE Select NP_000029.2:p.Pro1665=
NM_001127510.3:c.4994C= NP_001120982.1:p.Pro1665=
NM_001127511.3:c.4940C= NP_001120983.2:p.Pro1647=
NM_001354895.2:c.4994C= NP_001341824.1:p.Pro1665=
NM_001354896.2:c.5048C= NP_001341825.1:p.Pro1683=
NM_001354897.2:c.5024C= NP_001341826.1:p.Pro1675=
NM_001354898.2:c.4919C= NP_001341827.1:p.Pro1640=
NM_001354899.2:c.4910C= NP_001341828.1:p.Pro1637=
NM_001354900.2:c.4871C= NP_001341829.1:p.Pro1624=
NM_001354901.2:c.4817C= NP_001341830.1:p.Pro1606=
NM_001354902.2:c.4721C= NP_001341831.1:p.Pro1574=
NM_001354903.2:c.4691C= NP_001341832.1:p.Pro1564=
NM_001354904.2:c.4616C= NP_001341833.1:p.Pro1539=
NM_001354905.2:c.4514C= NP_001341834.1:p.Pro1505=
NM_001354906.2:c.4145C= NP_001341835.1:p.Pro1382=