Canonical Allele Identifier: CA1680191917
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024819T= , CM000668.2:g.167024819T= GRCh38
NC_000006.11:g.167438307T= , CM000668.1:g.167438307T= GRCh37
NC_000006.10:g.167358297T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.784T= ENSP00000230248.6:p.Ser262=
ENST00000488525.2:c.840T= ENSP00000516042.1:p.Pro280=
ENST00000609590.2:n.1716T=
ENST00000704900.1:c.421T= ENSP00000516059.1:p.Ser141=
ENST00000704901.1:c.*431T= ENSP00000516060.1:n.*431T=
ENST00000704959.1:n.1109T=
ENST00000704982.1:n.1554T=
ENST00000704985.1:n.1950T=
ENST00000704986.1:n.1950T=
ENST00000705029.1:n.1675T=
ENST00000705059.1:n.1499T=
ENST00000705168.1:c.97T= ENSP00000516071.1:p.Ser33=
ENST00000705169.1:c.97T= ENSP00000516072.1:p.Ser33=
ENST00000705170.1:c.97T= ENSP00000516073.1:p.Ser33=
ENST00000705171.1:n.889T=
ENST00000705173.1:c.*153T= ENSP00000516075.1:n.*153T=
ENST00000705175.1:c.970T= ENSP00000516077.1:p.Ser324=
ENST00000705176.1:c.1030T= ENSP00000516078.1:p.Ser344=
ENST00000705177.1:c.*428T= ENSP00000516079.1:n.*428T=
ENST00000705178.1:c.367T= ENSP00000516080.1:p.Ser123=
ENST00000705179.1:c.562T= ENSP00000516081.1:p.Ser188=
ENST00000705180.1:c.502T= ENSP00000516082.1:p.Ser168=
ENST00000705235.1:c.844T= ENSP00000516093.1:p.Ser282=
ENST00000705236.1:c.784T= ENSP00000516094.1:p.Ser262=
ENST00000705237.1:c.502T= ENSP00000516095.1:p.Ser168=
ENST00000705238.1:c.703T= ENSP00000516096.1:p.Ser235=
ENST00000705239.1:c.781T= ENSP00000516097.1:p.Ser261=
ENST00000705240.1:c.*453T= ENSP00000516098.1:n.*453T=
ENST00000705241.1:c.780T= ENSP00000516099.1:p.Pro260=
ENST00000705242.1:c.781T= ENSP00000516100.1:p.Ser261=
ENST00000705249.1:c.784T= ENSP00000516101.1:p.Ser262=
ENST00000705250.1:c.562T= ENSP00000516102.1:p.Ser188=
ENST00000705251.1:c.*431T= ENSP00000516103.1:n.*431T=
ENST00000705252.1:c.*254T= ENSP00000516104.1:n.*254T=
ENST00000705253.1:c.*254T= ENSP00000516105.1:n.*254T=
ENST00000705254.1:c.391T= ENSP00000516106.1:p.Ser131=
ENST00000705255.1:n.1410T=
ENST00000705256.1:c.841T= ENSP00000516107.1:p.Ser281=
ENST00000366847.9:c.844T= MANE Select ENSP00000355812.3:p.Ser282=
ENST00000349556.4:c.784T= ENSP00000230248.6:p.Ser262=
ENST00000366847.8:c.844T= ENSP00000355812.3:p.Ser282=
ENST00000488525.1:n.30T=
ENST00000496181.1:n.248T=
ENST00000622353.4:c.703T= ENSP00000479115.1:p.Ser235=
NM_001278690.1:c.703T= NP_001265619.1:p.Ser235=
NM_007045.3:c.844T= NP_008976.1:p.Ser282=
NM_194429.2:c.784T= NP_919410.1:p.Ser262=
NM_007045.4:c.844T= MANE Select NP_008976.1:p.Ser282=
NM_194429.3:c.784T= NP_919410.1:p.Ser262=
NM_001278690.2:c.703T= NP_001265619.1:p.Ser235=