Canonical Allele Identifier: CA1680192093
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024926C= , CM000668.2:g.167024926C= GRCh38
NC_000006.11:g.167438414C= , CM000668.1:g.167438414C= GRCh37
NC_000006.10:g.167358404C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.859+32C= ENSP00000230248.6:n.859+32C=
ENST00000488525.2:c.*51+32C= ENSP00000516042.1:n.*51+32C=
ENST00000609590.2:n.1791+32C=
ENST00000704900.1:c.496+32C= ENSP00000516059.1:n.496+32C=
ENST00000704901.1:c.*506+32C= ENSP00000516060.1:n.*506+32C=
ENST00000704959.1:n.1184+32C=
ENST00000704982.1:n.1629+32C=
ENST00000704985.1:n.2025+32C=
ENST00000704986.1:n.2025+32C=
ENST00000705029.1:n.1750+32C=
ENST00000705059.1:n.1574+32C=
ENST00000705168.1:c.172+32C= ENSP00000516071.1:n.172+32C=
ENST00000705169.1:c.172+32C= ENSP00000516072.1:n.172+32C=
ENST00000705170.1:c.172+32C= ENSP00000516073.1:n.172+32C=
ENST00000705171.1:n.964+32C=
ENST00000705173.1:c.*228+32C= ENSP00000516075.1:n.*228+32C=
ENST00000705175.1:c.1045+32C= ENSP00000516077.1:n.1045+32C=
ENST00000705176.1:c.1105+32C= ENSP00000516078.1:n.1105+32C=
ENST00000705177.1:c.*503+32C= ENSP00000516079.1:n.*503+32C=
ENST00000705178.1:c.442+32C= ENSP00000516080.1:n.442+32C=
ENST00000705179.1:c.637+32C= ENSP00000516081.1:n.637+32C=
ENST00000705180.1:c.577+32C= ENSP00000516082.1:n.577+32C=
ENST00000705235.1:c.919+32C= ENSP00000516093.1:n.919+32C=
ENST00000705236.1:c.859+32C= ENSP00000516094.1:n.859+32C=
ENST00000705237.1:c.577+32C= ENSP00000516095.1:n.577+32C=
ENST00000705238.1:c.778+32C= ENSP00000516096.1:n.778+32C=
ENST00000705239.1:c.856+32C= ENSP00000516097.1:n.856+32C=
ENST00000705240.1:c.*528+32C= ENSP00000516098.1:n.*528+32C=
ENST00000705241.1:c.*51+32C= ENSP00000516099.1:n.*51+32C=
ENST00000705242.1:c.856+32C= ENSP00000516100.1:n.856+32C=
ENST00000705249.1:c.859+32C= ENSP00000516101.1:n.859+32C=
ENST00000705250.1:c.637+32C= ENSP00000516102.1:n.637+32C=
ENST00000705251.1:c.*506+32C= ENSP00000516103.1:n.*506+32C=
ENST00000705252.1:c.*329+32C= ENSP00000516104.1:n.*329+32C=
ENST00000705253.1:c.*329+32C= ENSP00000516105.1:n.*329+32C=
ENST00000705254.1:c.466+32C= ENSP00000516106.1:n.466+32C=
ENST00000705255.1:n.1485+32C=
ENST00000705256.1:c.916+32C= ENSP00000516107.1:n.916+32C=
ENST00000366847.9:c.919+32C= MANE Select ENSP00000355812.3:n.919+32C=
ENST00000349556.4:c.859+32C= ENSP00000230248.6:n.859+32C=
ENST00000366847.8:c.919+32C= ENSP00000355812.3:n.919+32C=
ENST00000488525.1:n.105+32C=
ENST00000496181.1:n.355C=
ENST00000622353.4:c.778+32C= ENSP00000479115.1:n.778+32C=
NM_001278690.1:c.778+32C= NP_001265619.1:n.778+32C=
NM_007045.3:c.919+32C= NP_008976.1:n.919+32C=
NM_194429.2:c.859+32C= NP_919410.1:n.859+32C=
NM_007045.4:c.919+32C= MANE Select NP_008976.1:n.919+32C=
NM_194429.3:c.859+32C= NP_919410.1:n.859+32C=
NM_001278690.2:c.778+32C= NP_001265619.1:n.778+32C=