Canonical Allele Identifier: CA1680191952
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024832C= , CM000668.2:g.167024832C= GRCh38
NC_000006.11:g.167438320C= , CM000668.1:g.167438320C= GRCh37
NC_000006.10:g.167358310C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.797C= ENSP00000230248.6:p.Ala266=
ENST00000488525.2:c.853C= ENSP00000516042.1:p.His285=
ENST00000609590.2:n.1729C=
ENST00000704900.1:c.434C= ENSP00000516059.1:p.Ala145=
ENST00000704901.1:c.*444C= ENSP00000516060.1:n.*444C=
ENST00000704959.1:n.1122C=
ENST00000704982.1:n.1567C=
ENST00000704985.1:n.1963C=
ENST00000704986.1:n.1963C=
ENST00000705029.1:n.1688C=
ENST00000705059.1:n.1512C=
ENST00000705168.1:c.110C= ENSP00000516071.1:p.Ala37=
ENST00000705169.1:c.110C= ENSP00000516072.1:p.Ala37=
ENST00000705170.1:c.110C= ENSP00000516073.1:p.Ala37=
ENST00000705171.1:n.902C=
ENST00000705173.1:c.*166C= ENSP00000516075.1:n.*166C=
ENST00000705175.1:c.983C= ENSP00000516077.1:p.Ala328=
ENST00000705176.1:c.1043C= ENSP00000516078.1:p.Ala348=
ENST00000705177.1:c.*441C= ENSP00000516079.1:n.*441C=
ENST00000705178.1:c.380C= ENSP00000516080.1:p.Ala127=
ENST00000705179.1:c.575C= ENSP00000516081.1:p.Ala192=
ENST00000705180.1:c.515C= ENSP00000516082.1:p.Ala172=
ENST00000705235.1:c.857C= ENSP00000516093.1:p.Ala286=
ENST00000705236.1:c.797C= ENSP00000516094.1:p.Ala266=
ENST00000705237.1:c.515C= ENSP00000516095.1:p.Ala172=
ENST00000705238.1:c.716C= ENSP00000516096.1:p.Ala239=
ENST00000705239.1:c.794C= ENSP00000516097.1:p.Ala265=
ENST00000705240.1:c.*466C= ENSP00000516098.1:n.*466C=
ENST00000705241.1:c.793C= ENSP00000516099.1:p.His265=
ENST00000705242.1:c.794C= ENSP00000516100.1:p.Ala265=
ENST00000705249.1:c.797C= ENSP00000516101.1:p.Ala266=
ENST00000705250.1:c.575C= ENSP00000516102.1:p.Ala192=
ENST00000705251.1:c.*444C= ENSP00000516103.1:n.*444C=
ENST00000705252.1:c.*267C= ENSP00000516104.1:n.*267C=
ENST00000705253.1:c.*267C= ENSP00000516105.1:n.*267C=
ENST00000705254.1:c.404C= ENSP00000516106.1:p.Ala135=
ENST00000705255.1:n.1423C=
ENST00000705256.1:c.854C= ENSP00000516107.1:p.Ala285=
ENST00000366847.9:c.857C= MANE Select ENSP00000355812.3:p.Ala286=
ENST00000349556.4:c.797C= ENSP00000230248.6:p.Ala266=
ENST00000366847.8:c.857C= ENSP00000355812.3:p.Ala286=
ENST00000488525.1:n.43C=
ENST00000496181.1:n.261C=
ENST00000622353.4:c.716C= ENSP00000479115.1:p.Ala239=
NM_001278690.1:c.716C= NP_001265619.1:p.Ala239=
NM_007045.3:c.857C= NP_008976.1:p.Ala286=
NM_194429.2:c.797C= NP_919410.1:p.Ala266=
NM_007045.4:c.857C= MANE Select NP_008976.1:p.Ala286=
NM_194429.3:c.797C= NP_919410.1:p.Ala266=
NM_001278690.2:c.716C= NP_001265619.1:p.Ala239=