Canonical Allele Identifier: CA1680191863
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024783A= , CM000668.2:g.167024783A= GRCh38
NC_000006.11:g.167438271A= , CM000668.1:g.167438271A= GRCh37
NC_000006.10:g.167358261A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.748A= ENSP00000230248.6:p.Arg250=
ENST00000488525.2:c.804A= ENSP00000516042.1:p.Gly268=
ENST00000609590.2:n.1682-2A=
ENST00000704900.1:c.385A= ENSP00000516059.1:p.Arg129=
ENST00000704901.1:c.*395A= ENSP00000516060.1:n.*395A=
ENST00000704959.1:n.1073A=
ENST00000704982.1:n.1518A=
ENST00000704985.1:n.1914A=
ENST00000704986.1:n.1914A=
ENST00000705029.1:n.1639A=
ENST00000705059.1:n.1463A=
ENST00000705168.1:c.61A= ENSP00000516071.1:p.Arg21=
ENST00000705169.1:c.61A= ENSP00000516072.1:p.Arg21=
ENST00000705170.1:c.61A= ENSP00000516073.1:p.Arg21=
ENST00000705171.1:n.853A=
ENST00000705173.1:c.*117A= ENSP00000516075.1:n.*117A=
ENST00000705175.1:c.934A= ENSP00000516077.1:p.Arg312=
ENST00000705176.1:c.994A= ENSP00000516078.1:p.Arg332=
ENST00000705177.1:c.*392A= ENSP00000516079.1:n.*392A=
ENST00000705178.1:c.331A= ENSP00000516080.1:p.Arg111=
ENST00000705179.1:c.526A= ENSP00000516081.1:p.Arg176=
ENST00000705180.1:c.466A= ENSP00000516082.1:p.Arg156=
ENST00000705235.1:c.808A= ENSP00000516093.1:p.Arg270=
ENST00000705236.1:c.748A= ENSP00000516094.1:p.Arg250=
ENST00000705237.1:c.466A= ENSP00000516095.1:p.Arg156=
ENST00000705238.1:c.667A= ENSP00000516096.1:p.Arg223=
ENST00000705239.1:c.747-2A= ENSP00000516097.1:n.747-2A=
ENST00000705240.1:c.*417A= ENSP00000516098.1:n.*417A=
ENST00000705241.1:c.744A= ENSP00000516099.1:p.Gly248=
ENST00000705242.1:c.745A= ENSP00000516100.1:p.Arg249=
ENST00000705249.1:c.748A= ENSP00000516101.1:p.Arg250=
ENST00000705250.1:c.526A= ENSP00000516102.1:p.Arg176=
ENST00000705251.1:c.*395A= ENSP00000516103.1:n.*395A=
ENST00000705252.1:c.*218A= ENSP00000516104.1:n.*218A=
ENST00000705253.1:c.*218A= ENSP00000516105.1:n.*218A=
ENST00000705254.1:c.355A= ENSP00000516106.1:p.Arg119=
ENST00000705255.1:n.1374A=
ENST00000705256.1:c.807-2A= ENSP00000516107.1:n.807-2A=
ENST00000366847.9:c.808A= MANE Select ENSP00000355812.3:p.Arg270=
ENST00000349556.4:c.748A= ENSP00000230248.6:p.Arg250=
ENST00000366847.8:c.808A= ENSP00000355812.3:p.Arg270=
ENST00000496181.1:n.212A=
ENST00000622353.4:c.667A= ENSP00000479115.1:p.Arg223=
NM_001278690.1:c.667A= NP_001265619.1:p.Arg223=
NM_007045.3:c.808A= NP_008976.1:p.Arg270=
NM_194429.2:c.748A= NP_919410.1:p.Arg250=
NM_007045.4:c.808A= MANE Select NP_008976.1:p.Arg270=
NM_194429.3:c.748A= NP_919410.1:p.Arg250=
NM_001278690.2:c.667A= NP_001265619.1:p.Arg223=