Canonical Allele Identifier: CA571931146
Gene: CEP43 HGNC NCBI

Linked Data

dbSNP Id: rs1562530129

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024918_167025002dup , CM000668.2:g.167024918_167025002dup GRCh38
NC_000006.11:g.167438406_167438490dup , CM000668.1:g.167438406_167438490dup GRCh37
NC_000006.10:g.167358396_167358480dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.859+24_859+108dup ENSP00000230248.6:n.859+24_859+108dup
ENST00000488525.2:c.*51+24_*51+108dup ENSP00000516042.1:n.*51+24_*51+108dup
ENST00000609590.2:n.1791+24_1791+108dup
ENST00000704900.1:c.496+24_496+108dup ENSP00000516059.1:n.496+24_496+108dup
ENST00000704901.1:c.*506+24_*506+108dup ENSP00000516060.1:n.*506+24_*506+108dup
ENST00000704959.1:n.1184+24_1184+108dup
ENST00000704982.1:n.1629+24_1629+108dup
ENST00000704985.1:n.2025+24_2025+108dup
ENST00000704986.1:n.2025+24_2025+108dup
ENST00000705029.1:n.1750+24_1750+108dup
ENST00000705059.1:n.1574+24_1574+108dup
ENST00000705168.1:c.172+24_172+108dup ENSP00000516071.1:n.172+24_172+108dup
ENST00000705169.1:c.172+24_172+108dup ENSP00000516072.1:n.172+24_172+108dup
ENST00000705170.1:c.172+24_172+108dup ENSP00000516073.1:n.172+24_172+108dup
ENST00000705171.1:n.964+24_964+108dup
ENST00000705173.1:c.*228+24_*228+108dup ENSP00000516075.1:n.*228+24_*228+108dup
ENST00000705175.1:c.1045+24_1045+108dup ENSP00000516077.1:n.1045+24_1045+108dup
ENST00000705176.1:c.1105+24_1105+108dup ENSP00000516078.1:n.1105+24_1105+108dup
ENST00000705177.1:c.*503+24_*503+108dup ENSP00000516079.1:n.*503+24_*503+108dup
ENST00000705178.1:c.442+24_442+108dup ENSP00000516080.1:n.442+24_442+108dup
ENST00000705179.1:c.637+24_637+108dup ENSP00000516081.1:n.637+24_637+108dup
ENST00000705180.1:c.577+24_577+108dup ENSP00000516082.1:n.577+24_577+108dup
ENST00000705235.1:c.919+24_919+108dup ENSP00000516093.1:n.919+24_919+108dup
ENST00000705236.1:c.859+24_859+108dup ENSP00000516094.1:n.859+24_859+108dup
ENST00000705237.1:c.577+24_577+108dup ENSP00000516095.1:n.577+24_577+108dup
ENST00000705238.1:c.778+24_778+108dup ENSP00000516096.1:n.778+24_778+108dup
ENST00000705239.1:c.856+24_856+108dup ENSP00000516097.1:n.856+24_856+108dup
ENST00000705240.1:c.*528+24_*528+108dup ENSP00000516098.1:n.*528+24_*528+108dup
ENST00000705241.1:c.*51+24_*51+108dup ENSP00000516099.1:n.*51+24_*51+108dup
ENST00000705242.1:c.856+24_856+108dup ENSP00000516100.1:n.856+24_856+108dup
ENST00000705249.1:c.859+24_859+108dup ENSP00000516101.1:n.859+24_859+108dup
ENST00000705250.1:c.637+24_637+108dup ENSP00000516102.1:n.637+24_637+108dup
ENST00000705251.1:c.*506+24_*506+108dup ENSP00000516103.1:n.*506+24_*506+108dup
ENST00000705252.1:c.*329+24_*329+108dup ENSP00000516104.1:n.*329+24_*329+108dup
ENST00000705253.1:c.*329+24_*329+108dup ENSP00000516105.1:n.*329+24_*329+108dup
ENST00000705254.1:c.466+24_466+108dup ENSP00000516106.1:n.466+24_466+108dup
ENST00000705255.1:n.1485+24_1485+108dup
ENST00000705256.1:c.916+24_916+108dup ENSP00000516107.1:n.916+24_916+108dup
ENST00000366847.9:c.919+24_919+108dup MANE Select ENSP00000355812.3:n.919+24_919+108dup
ENST00000349556.4:c.859+24_859+108dup ENSP00000230248.6:n.859+24_859+108dup
ENST00000366847.8:c.919+24_919+108dup ENSP00000355812.3:n.919+24_919+108dup
ENST00000488525.1:n.105+24_105+108dup
ENST00000496181.1:n.347_431dup
ENST00000622353.4:c.778+24_778+108dup ENSP00000479115.1:n.778+24_778+108dup
NM_001278690.1:c.778+24_778+108dup NP_001265619.1:n.778+24_778+108dup
NM_007045.3:c.919+24_919+108dup NP_008976.1:n.919+24_919+108dup
NM_194429.2:c.859+24_859+108dup NP_919410.1:n.859+24_859+108dup
NM_007045.4:c.919+24_919+108dup MANE Select NP_008976.1:n.919+24_919+108dup
NM_194429.3:c.859+24_859+108dup NP_919410.1:n.859+24_859+108dup
NM_001278690.2:c.778+24_778+108dup NP_001265619.1:n.778+24_778+108dup