Canonical Allele Identifier: CA1680191875
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024793C= , CM000668.2:g.167024793C= GRCh38
NC_000006.11:g.167438281C= , CM000668.1:g.167438281C= GRCh37
NC_000006.10:g.167358271C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.758C= ENSP00000230248.6:p.Pro253=
ENST00000488525.2:c.814C= ENSP00000516042.1:p.Leu272=
ENST00000609590.2:n.1690C=
ENST00000704900.1:c.395C= ENSP00000516059.1:p.Pro132=
ENST00000704901.1:c.*405C= ENSP00000516060.1:n.*405C=
ENST00000704959.1:n.1083C=
ENST00000704982.1:n.1528C=
ENST00000704985.1:n.1924C=
ENST00000704986.1:n.1924C=
ENST00000705029.1:n.1649C=
ENST00000705059.1:n.1473C=
ENST00000705168.1:c.71C= ENSP00000516071.1:p.Pro24=
ENST00000705169.1:c.71C= ENSP00000516072.1:p.Pro24=
ENST00000705170.1:c.71C= ENSP00000516073.1:p.Pro24=
ENST00000705171.1:n.863C=
ENST00000705173.1:c.*127C= ENSP00000516075.1:n.*127C=
ENST00000705175.1:c.944C= ENSP00000516077.1:p.Pro315=
ENST00000705176.1:c.1004C= ENSP00000516078.1:p.Pro335=
ENST00000705177.1:c.*402C= ENSP00000516079.1:n.*402C=
ENST00000705178.1:c.341C= ENSP00000516080.1:p.Pro114=
ENST00000705179.1:c.536C= ENSP00000516081.1:p.Pro179=
ENST00000705180.1:c.476C= ENSP00000516082.1:p.Pro159=
ENST00000705235.1:c.818C= ENSP00000516093.1:p.Pro273=
ENST00000705236.1:c.758C= ENSP00000516094.1:p.Pro253=
ENST00000705237.1:c.476C= ENSP00000516095.1:p.Pro159=
ENST00000705238.1:c.677C= ENSP00000516096.1:p.Pro226=
ENST00000705239.1:c.755C= ENSP00000516097.1:p.Pro252=
ENST00000705240.1:c.*427C= ENSP00000516098.1:n.*427C=
ENST00000705241.1:c.754C= ENSP00000516099.1:p.Leu252=
ENST00000705242.1:c.755C= ENSP00000516100.1:p.Pro252=
ENST00000705249.1:c.758C= ENSP00000516101.1:p.Pro253=
ENST00000705250.1:c.536C= ENSP00000516102.1:p.Pro179=
ENST00000705251.1:c.*405C= ENSP00000516103.1:n.*405C=
ENST00000705252.1:c.*228C= ENSP00000516104.1:n.*228C=
ENST00000705253.1:c.*228C= ENSP00000516105.1:n.*228C=
ENST00000705254.1:c.365C= ENSP00000516106.1:p.Pro122=
ENST00000705255.1:n.1384C=
ENST00000705256.1:c.815C= ENSP00000516107.1:p.Pro272=
ENST00000366847.9:c.818C= MANE Select ENSP00000355812.3:p.Pro273=
ENST00000349556.4:c.758C= ENSP00000230248.6:p.Pro253=
ENST00000366847.8:c.818C= ENSP00000355812.3:p.Pro273=
ENST00000488525.1:n.4C=
ENST00000496181.1:n.222C=
ENST00000622353.4:c.677C= ENSP00000479115.1:p.Pro226=
NM_001278690.1:c.677C= NP_001265619.1:p.Pro226=
NM_007045.3:c.818C= NP_008976.1:p.Pro273=
NM_194429.2:c.758C= NP_919410.1:p.Pro253=
NM_007045.4:c.818C= MANE Select NP_008976.1:p.Pro273=
NM_194429.3:c.758C= NP_919410.1:p.Pro253=
NM_001278690.2:c.677C= NP_001265619.1:p.Pro226=