Canonical Allele Identifier: CA1680191902
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024804G= , CM000668.2:g.167024804G= GRCh38
NC_000006.11:g.167438292G= , CM000668.1:g.167438292G= GRCh37
NC_000006.10:g.167358282G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.769G= ENSP00000230248.6:p.Ala257=
ENST00000488525.2:c.825G= ENSP00000516042.1:p.Lys275=
ENST00000609590.2:n.1701G=
ENST00000704900.1:c.406G= ENSP00000516059.1:p.Ala136=
ENST00000704901.1:c.*416G= ENSP00000516060.1:n.*416G=
ENST00000704959.1:n.1094G=
ENST00000704982.1:n.1539G=
ENST00000704985.1:n.1935G=
ENST00000704986.1:n.1935G=
ENST00000705029.1:n.1660G=
ENST00000705059.1:n.1484G=
ENST00000705168.1:c.82G= ENSP00000516071.1:p.Ala28=
ENST00000705169.1:c.82G= ENSP00000516072.1:p.Ala28=
ENST00000705170.1:c.82G= ENSP00000516073.1:p.Ala28=
ENST00000705171.1:n.874G=
ENST00000705173.1:c.*138G= ENSP00000516075.1:n.*138G=
ENST00000705175.1:c.955G= ENSP00000516077.1:p.Ala319=
ENST00000705176.1:c.1015G= ENSP00000516078.1:p.Ala339=
ENST00000705177.1:c.*413G= ENSP00000516079.1:n.*413G=
ENST00000705178.1:c.352G= ENSP00000516080.1:p.Ala118=
ENST00000705179.1:c.547G= ENSP00000516081.1:p.Ala183=
ENST00000705180.1:c.487G= ENSP00000516082.1:p.Ala163=
ENST00000705235.1:c.829G= ENSP00000516093.1:p.Ala277=
ENST00000705236.1:c.769G= ENSP00000516094.1:p.Ala257=
ENST00000705237.1:c.487G= ENSP00000516095.1:p.Ala163=
ENST00000705238.1:c.688G= ENSP00000516096.1:p.Ala230=
ENST00000705239.1:c.766G= ENSP00000516097.1:p.Ala256=
ENST00000705240.1:c.*438G= ENSP00000516098.1:n.*438G=
ENST00000705241.1:c.765G= ENSP00000516099.1:p.Lys255=
ENST00000705242.1:c.766G= ENSP00000516100.1:p.Ala256=
ENST00000705249.1:c.769G= ENSP00000516101.1:p.Ala257=
ENST00000705250.1:c.547G= ENSP00000516102.1:p.Ala183=
ENST00000705251.1:c.*416G= ENSP00000516103.1:n.*416G=
ENST00000705252.1:c.*239G= ENSP00000516104.1:n.*239G=
ENST00000705253.1:c.*239G= ENSP00000516105.1:n.*239G=
ENST00000705254.1:c.376G= ENSP00000516106.1:p.Ala126=
ENST00000705255.1:n.1395G=
ENST00000705256.1:c.826G= ENSP00000516107.1:p.Ala276=
ENST00000366847.9:c.829G= MANE Select ENSP00000355812.3:p.Ala277=
ENST00000349556.4:c.769G= ENSP00000230248.6:p.Ala257=
ENST00000366847.8:c.829G= ENSP00000355812.3:p.Ala277=
ENST00000488525.1:n.15G=
ENST00000496181.1:n.233G=
ENST00000622353.4:c.688G= ENSP00000479115.1:p.Ala230=
NM_001278690.1:c.688G= NP_001265619.1:p.Ala230=
NM_007045.3:c.829G= NP_008976.1:p.Ala277=
NM_194429.2:c.769G= NP_919410.1:p.Ala257=
NM_007045.4:c.829G= MANE Select NP_008976.1:p.Ala277=
NM_194429.3:c.769G= NP_919410.1:p.Ala257=
NM_001278690.2:c.688G= NP_001265619.1:p.Ala230=