Canonical Allele Identifier: CA1680192010
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024868G= , CM000668.2:g.167024868G= GRCh38
NC_000006.11:g.167438356G= , CM000668.1:g.167438356G= GRCh37
NC_000006.10:g.167358346G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.833G= ENSP00000230248.6:p.Gly278=
ENST00000488525.2:c.*25G= ENSP00000516042.1:n.*25G=
ENST00000609590.2:n.1765G=
ENST00000704900.1:c.470G= ENSP00000516059.1:p.Gly157=
ENST00000704901.1:c.*480G= ENSP00000516060.1:n.*480G=
ENST00000704959.1:n.1158G=
ENST00000704982.1:n.1603G=
ENST00000704985.1:n.1999G=
ENST00000704986.1:n.1999G=
ENST00000705029.1:n.1724G=
ENST00000705059.1:n.1548G=
ENST00000705168.1:c.146G= ENSP00000516071.1:p.Gly49=
ENST00000705169.1:c.146G= ENSP00000516072.1:p.Gly49=
ENST00000705170.1:c.146G= ENSP00000516073.1:p.Gly49=
ENST00000705171.1:n.938G=
ENST00000705173.1:c.*202G= ENSP00000516075.1:n.*202G=
ENST00000705175.1:c.1019G= ENSP00000516077.1:p.Gly340=
ENST00000705176.1:c.1079G= ENSP00000516078.1:p.Gly360=
ENST00000705177.1:c.*477G= ENSP00000516079.1:n.*477G=
ENST00000705178.1:c.416G= ENSP00000516080.1:p.Gly139=
ENST00000705179.1:c.611G= ENSP00000516081.1:p.Gly204=
ENST00000705180.1:c.551G= ENSP00000516082.1:p.Gly184=
ENST00000705235.1:c.893G= ENSP00000516093.1:p.Gly298=
ENST00000705236.1:c.833G= ENSP00000516094.1:p.Gly278=
ENST00000705237.1:c.551G= ENSP00000516095.1:p.Gly184=
ENST00000705238.1:c.752G= ENSP00000516096.1:p.Gly251=
ENST00000705239.1:c.830G= ENSP00000516097.1:p.Gly277=
ENST00000705240.1:c.*502G= ENSP00000516098.1:n.*502G=
ENST00000705241.1:c.*25G= ENSP00000516099.1:n.*25G=
ENST00000705242.1:c.830G= ENSP00000516100.1:p.Gly277=
ENST00000705249.1:c.833G= ENSP00000516101.1:p.Gly278=
ENST00000705250.1:c.611G= ENSP00000516102.1:p.Gly204=
ENST00000705251.1:c.*480G= ENSP00000516103.1:n.*480G=
ENST00000705252.1:c.*303G= ENSP00000516104.1:n.*303G=
ENST00000705253.1:c.*303G= ENSP00000516105.1:n.*303G=
ENST00000705254.1:c.440G= ENSP00000516106.1:p.Gly147=
ENST00000705255.1:n.1459G=
ENST00000705256.1:c.890G= ENSP00000516107.1:p.Gly297=
ENST00000366847.9:c.893G= MANE Select ENSP00000355812.3:p.Gly298=
ENST00000349556.4:c.833G= ENSP00000230248.6:p.Gly278=
ENST00000366847.8:c.893G= ENSP00000355812.3:p.Gly298=
ENST00000488525.1:n.79G=
ENST00000496181.1:n.297G=
ENST00000622353.4:c.752G= ENSP00000479115.1:p.Gly251=
NM_001278690.1:c.752G= NP_001265619.1:p.Gly251=
NM_007045.3:c.893G= NP_008976.1:p.Gly298=
NM_194429.2:c.833G= NP_919410.1:p.Gly278=
NM_007045.4:c.893G= MANE Select NP_008976.1:p.Gly298=
NM_194429.3:c.833G= NP_919410.1:p.Gly278=
NM_001278690.2:c.752G= NP_001265619.1:p.Gly251=