Canonical Allele Identifier: CA1680191914
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024818C= , CM000668.2:g.167024818C= GRCh38
NC_000006.11:g.167438306C= , CM000668.1:g.167438306C= GRCh37
NC_000006.10:g.167358296C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.783C= ENSP00000230248.6:p.Ala261=
ENST00000488525.2:c.839C= ENSP00000516042.1:p.Pro280=
ENST00000609590.2:n.1715C=
ENST00000704900.1:c.420C= ENSP00000516059.1:p.Ala140=
ENST00000704901.1:c.*430C= ENSP00000516060.1:n.*430C=
ENST00000704959.1:n.1108C=
ENST00000704982.1:n.1553C=
ENST00000704985.1:n.1949C=
ENST00000704986.1:n.1949C=
ENST00000705029.1:n.1674C=
ENST00000705059.1:n.1498C=
ENST00000705168.1:c.96C= ENSP00000516071.1:p.Ala32=
ENST00000705169.1:c.96C= ENSP00000516072.1:p.Ala32=
ENST00000705170.1:c.96C= ENSP00000516073.1:p.Ala32=
ENST00000705171.1:n.888C=
ENST00000705173.1:c.*152C= ENSP00000516075.1:n.*152C=
ENST00000705175.1:c.969C= ENSP00000516077.1:p.Ala323=
ENST00000705176.1:c.1029C= ENSP00000516078.1:p.Ala343=
ENST00000705177.1:c.*427C= ENSP00000516079.1:n.*427C=
ENST00000705178.1:c.366C= ENSP00000516080.1:p.Ala122=
ENST00000705179.1:c.561C= ENSP00000516081.1:p.Ala187=
ENST00000705180.1:c.501C= ENSP00000516082.1:p.Ala167=
ENST00000705235.1:c.843C= ENSP00000516093.1:p.Ala281=
ENST00000705236.1:c.783C= ENSP00000516094.1:p.Ala261=
ENST00000705237.1:c.501C= ENSP00000516095.1:p.Ala167=
ENST00000705238.1:c.702C= ENSP00000516096.1:p.Ala234=
ENST00000705239.1:c.780C= ENSP00000516097.1:p.Ala260=
ENST00000705240.1:c.*452C= ENSP00000516098.1:n.*452C=
ENST00000705241.1:c.779C= ENSP00000516099.1:p.Pro260=
ENST00000705242.1:c.780C= ENSP00000516100.1:p.Ala260=
ENST00000705249.1:c.783C= ENSP00000516101.1:p.Ala261=
ENST00000705250.1:c.561C= ENSP00000516102.1:p.Ala187=
ENST00000705251.1:c.*430C= ENSP00000516103.1:n.*430C=
ENST00000705252.1:c.*253C= ENSP00000516104.1:n.*253C=
ENST00000705253.1:c.*253C= ENSP00000516105.1:n.*253C=
ENST00000705254.1:c.390C= ENSP00000516106.1:p.Ala130=
ENST00000705255.1:n.1409C=
ENST00000705256.1:c.840C= ENSP00000516107.1:p.Ala280=
ENST00000366847.9:c.843C= MANE Select ENSP00000355812.3:p.Ala281=
ENST00000349556.4:c.783C= ENSP00000230248.6:p.Ala261=
ENST00000366847.8:c.843C= ENSP00000355812.3:p.Ala281=
ENST00000488525.1:n.29C=
ENST00000496181.1:n.247C=
ENST00000622353.4:c.702C= ENSP00000479115.1:p.Ala234=
NM_001278690.1:c.702C= NP_001265619.1:p.Ala234=
NM_007045.3:c.843C= NP_008976.1:p.Ala281=
NM_194429.2:c.783C= NP_919410.1:p.Ala261=
NM_007045.4:c.843C= MANE Select NP_008976.1:p.Ala281=
NM_194429.3:c.783C= NP_919410.1:p.Ala261=
NM_001278690.2:c.702C= NP_001265619.1:p.Ala234=