Canonical Allele Identifier: CA1680192012
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024872C= , CM000668.2:g.167024872C= GRCh38
NC_000006.11:g.167438360C= , CM000668.1:g.167438360C= GRCh37
NC_000006.10:g.167358350C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.837C= ENSP00000230248.6:p.Ala279=
ENST00000488525.2:c.*29C= ENSP00000516042.1:n.*29C=
ENST00000609590.2:n.1769C=
ENST00000704900.1:c.474C= ENSP00000516059.1:p.Ala158=
ENST00000704901.1:c.*484C= ENSP00000516060.1:n.*484C=
ENST00000704959.1:n.1162C=
ENST00000704982.1:n.1607C=
ENST00000704985.1:n.2003C=
ENST00000704986.1:n.2003C=
ENST00000705029.1:n.1728C=
ENST00000705059.1:n.1552C=
ENST00000705168.1:c.150C= ENSP00000516071.1:p.Ala50=
ENST00000705169.1:c.150C= ENSP00000516072.1:p.Ala50=
ENST00000705170.1:c.150C= ENSP00000516073.1:p.Ala50=
ENST00000705171.1:n.942C=
ENST00000705173.1:c.*206C= ENSP00000516075.1:n.*206C=
ENST00000705175.1:c.1023C= ENSP00000516077.1:p.Ala341=
ENST00000705176.1:c.1083C= ENSP00000516078.1:p.Ala361=
ENST00000705177.1:c.*481C= ENSP00000516079.1:n.*481C=
ENST00000705178.1:c.420C= ENSP00000516080.1:p.Ala140=
ENST00000705179.1:c.615C= ENSP00000516081.1:p.Ala205=
ENST00000705180.1:c.555C= ENSP00000516082.1:p.Ala185=
ENST00000705235.1:c.897C= ENSP00000516093.1:p.Ala299=
ENST00000705236.1:c.837C= ENSP00000516094.1:p.Ala279=
ENST00000705237.1:c.555C= ENSP00000516095.1:p.Ala185=
ENST00000705238.1:c.756C= ENSP00000516096.1:p.Ala252=
ENST00000705239.1:c.834C= ENSP00000516097.1:p.Ala278=
ENST00000705240.1:c.*506C= ENSP00000516098.1:n.*506C=
ENST00000705241.1:c.*29C= ENSP00000516099.1:n.*29C=
ENST00000705242.1:c.834C= ENSP00000516100.1:p.Ala278=
ENST00000705249.1:c.837C= ENSP00000516101.1:p.Ala279=
ENST00000705250.1:c.615C= ENSP00000516102.1:p.Ala205=
ENST00000705251.1:c.*484C= ENSP00000516103.1:n.*484C=
ENST00000705252.1:c.*307C= ENSP00000516104.1:n.*307C=
ENST00000705253.1:c.*307C= ENSP00000516105.1:n.*307C=
ENST00000705254.1:c.444C= ENSP00000516106.1:p.Ala148=
ENST00000705255.1:n.1463C=
ENST00000705256.1:c.894C= ENSP00000516107.1:p.Ala298=
ENST00000366847.9:c.897C= MANE Select ENSP00000355812.3:p.Ala299=
ENST00000349556.4:c.837C= ENSP00000230248.6:p.Ala279=
ENST00000366847.8:c.897C= ENSP00000355812.3:p.Ala299=
ENST00000488525.1:n.83C=
ENST00000496181.1:n.301C=
ENST00000622353.4:c.756C= ENSP00000479115.1:p.Ala252=
NM_001278690.1:c.756C= NP_001265619.1:p.Ala252=
NM_007045.3:c.897C= NP_008976.1:p.Ala299=
NM_194429.2:c.837C= NP_919410.1:p.Ala279=
NM_007045.4:c.897C= MANE Select NP_008976.1:p.Ala299=
NM_194429.3:c.837C= NP_919410.1:p.Ala279=
NM_001278690.2:c.756C= NP_001265619.1:p.Ala252=