Canonical Allele Identifier: CA1680191887
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024797G= , CM000668.2:g.167024797G= GRCh38
NC_000006.11:g.167438285G= , CM000668.1:g.167438285G= GRCh37
NC_000006.10:g.167358275G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.762G= ENSP00000230248.6:p.Arg254=
ENST00000488525.2:c.818G= ENSP00000516042.1:p.Gly273=
ENST00000609590.2:n.1694G=
ENST00000704900.1:c.399G= ENSP00000516059.1:p.Arg133=
ENST00000704901.1:c.*409G= ENSP00000516060.1:n.*409G=
ENST00000704959.1:n.1087G=
ENST00000704982.1:n.1532G=
ENST00000704985.1:n.1928G=
ENST00000704986.1:n.1928G=
ENST00000705029.1:n.1653G=
ENST00000705059.1:n.1477G=
ENST00000705168.1:c.75G= ENSP00000516071.1:p.Arg25=
ENST00000705169.1:c.75G= ENSP00000516072.1:p.Arg25=
ENST00000705170.1:c.75G= ENSP00000516073.1:p.Arg25=
ENST00000705171.1:n.867G=
ENST00000705173.1:c.*131G= ENSP00000516075.1:n.*131G=
ENST00000705175.1:c.948G= ENSP00000516077.1:p.Arg316=
ENST00000705176.1:c.1008G= ENSP00000516078.1:p.Arg336=
ENST00000705177.1:c.*406G= ENSP00000516079.1:n.*406G=
ENST00000705178.1:c.345G= ENSP00000516080.1:p.Arg115=
ENST00000705179.1:c.540G= ENSP00000516081.1:p.Arg180=
ENST00000705180.1:c.480G= ENSP00000516082.1:p.Arg160=
ENST00000705235.1:c.822G= ENSP00000516093.1:p.Arg274=
ENST00000705236.1:c.762G= ENSP00000516094.1:p.Arg254=
ENST00000705237.1:c.480G= ENSP00000516095.1:p.Arg160=
ENST00000705238.1:c.681G= ENSP00000516096.1:p.Arg227=
ENST00000705239.1:c.759G= ENSP00000516097.1:p.Arg253=
ENST00000705240.1:c.*431G= ENSP00000516098.1:n.*431G=
ENST00000705241.1:c.758G= ENSP00000516099.1:p.Gly253=
ENST00000705242.1:c.759G= ENSP00000516100.1:p.Arg253=
ENST00000705249.1:c.762G= ENSP00000516101.1:p.Arg254=
ENST00000705250.1:c.540G= ENSP00000516102.1:p.Arg180=
ENST00000705251.1:c.*409G= ENSP00000516103.1:n.*409G=
ENST00000705252.1:c.*232G= ENSP00000516104.1:n.*232G=
ENST00000705253.1:c.*232G= ENSP00000516105.1:n.*232G=
ENST00000705254.1:c.369G= ENSP00000516106.1:p.Arg123=
ENST00000705255.1:n.1388G=
ENST00000705256.1:c.819G= ENSP00000516107.1:p.Arg273=
ENST00000366847.9:c.822G= MANE Select ENSP00000355812.3:p.Arg274=
ENST00000349556.4:c.762G= ENSP00000230248.6:p.Arg254=
ENST00000366847.8:c.822G= ENSP00000355812.3:p.Arg274=
ENST00000488525.1:n.8G=
ENST00000496181.1:n.226G=
ENST00000622353.4:c.681G= ENSP00000479115.1:p.Arg227=
NM_001278690.1:c.681G= NP_001265619.1:p.Arg227=
NM_007045.3:c.822G= NP_008976.1:p.Arg274=
NM_194429.2:c.762G= NP_919410.1:p.Arg254=
NM_007045.4:c.822G= MANE Select NP_008976.1:p.Arg274=
NM_194429.3:c.762G= NP_919410.1:p.Arg254=
NM_001278690.2:c.681G= NP_001265619.1:p.Arg227=