Canonical Allele Identifier: CA1680191937
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024826C= , CM000668.2:g.167024826C= GRCh38
NC_000006.11:g.167438314C= , CM000668.1:g.167438314C= GRCh37
NC_000006.10:g.167358304C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.791C= ENSP00000230248.6:p.Ser264=
ENST00000488525.2:c.847C= ENSP00000516042.1:p.Arg283=
ENST00000609590.2:n.1723C=
ENST00000704900.1:c.428C= ENSP00000516059.1:p.Ser143=
ENST00000704901.1:c.*438C= ENSP00000516060.1:n.*438C=
ENST00000704959.1:n.1116C=
ENST00000704982.1:n.1561C=
ENST00000704985.1:n.1957C=
ENST00000704986.1:n.1957C=
ENST00000705029.1:n.1682C=
ENST00000705059.1:n.1506C=
ENST00000705168.1:c.104C= ENSP00000516071.1:p.Ser35=
ENST00000705169.1:c.104C= ENSP00000516072.1:p.Ser35=
ENST00000705170.1:c.104C= ENSP00000516073.1:p.Ser35=
ENST00000705171.1:n.896C=
ENST00000705173.1:c.*160C= ENSP00000516075.1:n.*160C=
ENST00000705175.1:c.977C= ENSP00000516077.1:p.Ser326=
ENST00000705176.1:c.1037C= ENSP00000516078.1:p.Ser346=
ENST00000705177.1:c.*435C= ENSP00000516079.1:n.*435C=
ENST00000705178.1:c.374C= ENSP00000516080.1:p.Ser125=
ENST00000705179.1:c.569C= ENSP00000516081.1:p.Ser190=
ENST00000705180.1:c.509C= ENSP00000516082.1:p.Ser170=
ENST00000705235.1:c.851C= ENSP00000516093.1:p.Ser284=
ENST00000705236.1:c.791C= ENSP00000516094.1:p.Ser264=
ENST00000705237.1:c.509C= ENSP00000516095.1:p.Ser170=
ENST00000705238.1:c.710C= ENSP00000516096.1:p.Ser237=
ENST00000705239.1:c.788C= ENSP00000516097.1:p.Ser263=
ENST00000705240.1:c.*460C= ENSP00000516098.1:n.*460C=
ENST00000705241.1:c.787C= ENSP00000516099.1:p.Arg263=
ENST00000705242.1:c.788C= ENSP00000516100.1:p.Ser263=
ENST00000705249.1:c.791C= ENSP00000516101.1:p.Ser264=
ENST00000705250.1:c.569C= ENSP00000516102.1:p.Ser190=
ENST00000705251.1:c.*438C= ENSP00000516103.1:n.*438C=
ENST00000705252.1:c.*261C= ENSP00000516104.1:n.*261C=
ENST00000705253.1:c.*261C= ENSP00000516105.1:n.*261C=
ENST00000705254.1:c.398C= ENSP00000516106.1:p.Ser133=
ENST00000705255.1:n.1417C=
ENST00000705256.1:c.848C= ENSP00000516107.1:p.Ser283=
ENST00000366847.9:c.851C= MANE Select ENSP00000355812.3:p.Ser284=
ENST00000349556.4:c.791C= ENSP00000230248.6:p.Ser264=
ENST00000366847.8:c.851C= ENSP00000355812.3:p.Ser284=
ENST00000488525.1:n.37C=
ENST00000496181.1:n.255C=
ENST00000622353.4:c.710C= ENSP00000479115.1:p.Ser237=
NM_001278690.1:c.710C= NP_001265619.1:p.Ser237=
NM_007045.3:c.851C= NP_008976.1:p.Ser284=
NM_194429.2:c.791C= NP_919410.1:p.Ser264=
NM_007045.4:c.851C= MANE Select NP_008976.1:p.Ser284=
NM_194429.3:c.791C= NP_919410.1:p.Ser264=
NM_001278690.2:c.710C= NP_001265619.1:p.Ser237=