Canonical Allele Identifier: CA1680191992
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024857C= , CM000668.2:g.167024857C= GRCh38
NC_000006.11:g.167438345C= , CM000668.1:g.167438345C= GRCh37
NC_000006.10:g.167358335C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.822C= ENSP00000230248.6:p.Ser274=
ENST00000488525.2:c.*14C= ENSP00000516042.1:n.*14C=
ENST00000609590.2:n.1754C=
ENST00000704900.1:c.459C= ENSP00000516059.1:p.Ser153=
ENST00000704901.1:c.*469C= ENSP00000516060.1:n.*469C=
ENST00000704959.1:n.1147C=
ENST00000704982.1:n.1592C=
ENST00000704985.1:n.1988C=
ENST00000704986.1:n.1988C=
ENST00000705029.1:n.1713C=
ENST00000705059.1:n.1537C=
ENST00000705168.1:c.135C= ENSP00000516071.1:p.Ser45=
ENST00000705169.1:c.135C= ENSP00000516072.1:p.Ser45=
ENST00000705170.1:c.135C= ENSP00000516073.1:p.Ser45=
ENST00000705171.1:n.927C=
ENST00000705173.1:c.*191C= ENSP00000516075.1:n.*191C=
ENST00000705175.1:c.1008C= ENSP00000516077.1:p.Ser336=
ENST00000705176.1:c.1068C= ENSP00000516078.1:p.Ser356=
ENST00000705177.1:c.*466C= ENSP00000516079.1:n.*466C=
ENST00000705178.1:c.405C= ENSP00000516080.1:p.Ser135=
ENST00000705179.1:c.600C= ENSP00000516081.1:p.Ser200=
ENST00000705180.1:c.540C= ENSP00000516082.1:p.Ser180=
ENST00000705235.1:c.882C= ENSP00000516093.1:p.Ser294=
ENST00000705236.1:c.822C= ENSP00000516094.1:p.Ser274=
ENST00000705237.1:c.540C= ENSP00000516095.1:p.Ser180=
ENST00000705238.1:c.741C= ENSP00000516096.1:p.Ser247=
ENST00000705239.1:c.819C= ENSP00000516097.1:p.Ser273=
ENST00000705240.1:c.*491C= ENSP00000516098.1:n.*491C=
ENST00000705241.1:c.*14C= ENSP00000516099.1:n.*14C=
ENST00000705242.1:c.819C= ENSP00000516100.1:p.Ser273=
ENST00000705249.1:c.822C= ENSP00000516101.1:p.Ser274=
ENST00000705250.1:c.600C= ENSP00000516102.1:p.Ser200=
ENST00000705251.1:c.*469C= ENSP00000516103.1:n.*469C=
ENST00000705252.1:c.*292C= ENSP00000516104.1:n.*292C=
ENST00000705253.1:c.*292C= ENSP00000516105.1:n.*292C=
ENST00000705254.1:c.429C= ENSP00000516106.1:p.Ser143=
ENST00000705255.1:n.1448C=
ENST00000705256.1:c.879C= ENSP00000516107.1:p.Ser293=
ENST00000366847.9:c.882C= MANE Select ENSP00000355812.3:p.Ser294=
ENST00000349556.4:c.822C= ENSP00000230248.6:p.Ser274=
ENST00000366847.8:c.882C= ENSP00000355812.3:p.Ser294=
ENST00000488525.1:n.68C=
ENST00000496181.1:n.286C=
ENST00000622353.4:c.741C= ENSP00000479115.1:p.Ser247=
NM_001278690.1:c.741C= NP_001265619.1:p.Ser247=
NM_007045.3:c.882C= NP_008976.1:p.Ser294=
NM_194429.2:c.822C= NP_919410.1:p.Ser274=
NM_007045.4:c.882C= MANE Select NP_008976.1:p.Ser294=
NM_194429.3:c.822C= NP_919410.1:p.Ser274=
NM_001278690.2:c.741C= NP_001265619.1:p.Ser247=