Canonical Allele Identifier: CA1680192038
Gene: CEP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167024886A= , CM000668.2:g.167024886A= GRCh38
NC_000006.11:g.167438374A= , CM000668.1:g.167438374A= GRCh37
NC_000006.10:g.167358364A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349556.5:c.851A= ENSP00000230248.6:p.Asp284=
ENST00000488525.2:c.*43A= ENSP00000516042.1:n.*43A=
ENST00000609590.2:n.1783A=
ENST00000704900.1:c.488A= ENSP00000516059.1:p.Asp163=
ENST00000704901.1:c.*498A= ENSP00000516060.1:n.*498A=
ENST00000704959.1:n.1176A=
ENST00000704982.1:n.1621A=
ENST00000704985.1:n.2017A=
ENST00000704986.1:n.2017A=
ENST00000705029.1:n.1742A=
ENST00000705059.1:n.1566A=
ENST00000705168.1:c.164A= ENSP00000516071.1:p.Asp55=
ENST00000705169.1:c.164A= ENSP00000516072.1:p.Asp55=
ENST00000705170.1:c.164A= ENSP00000516073.1:p.Asp55=
ENST00000705171.1:n.956A=
ENST00000705173.1:c.*220A= ENSP00000516075.1:n.*220A=
ENST00000705175.1:c.1037A= ENSP00000516077.1:p.Asp346=
ENST00000705176.1:c.1097A= ENSP00000516078.1:p.Asp366=
ENST00000705177.1:c.*495A= ENSP00000516079.1:n.*495A=
ENST00000705178.1:c.434A= ENSP00000516080.1:p.Asp145=
ENST00000705179.1:c.629A= ENSP00000516081.1:p.Asp210=
ENST00000705180.1:c.569A= ENSP00000516082.1:p.Asp190=
ENST00000705235.1:c.911A= ENSP00000516093.1:p.Asp304=
ENST00000705236.1:c.851A= ENSP00000516094.1:p.Asp284=
ENST00000705237.1:c.569A= ENSP00000516095.1:p.Asp190=
ENST00000705238.1:c.770A= ENSP00000516096.1:p.Asp257=
ENST00000705239.1:c.848A= ENSP00000516097.1:p.Asp283=
ENST00000705240.1:c.*520A= ENSP00000516098.1:n.*520A=
ENST00000705241.1:c.*43A= ENSP00000516099.1:n.*43A=
ENST00000705242.1:c.848A= ENSP00000516100.1:p.Asp283=
ENST00000705249.1:c.851A= ENSP00000516101.1:p.Asp284=
ENST00000705250.1:c.629A= ENSP00000516102.1:p.Asp210=
ENST00000705251.1:c.*498A= ENSP00000516103.1:n.*498A=
ENST00000705252.1:c.*321A= ENSP00000516104.1:n.*321A=
ENST00000705253.1:c.*321A= ENSP00000516105.1:n.*321A=
ENST00000705254.1:c.458A= ENSP00000516106.1:p.Asp153=
ENST00000705255.1:n.1477A=
ENST00000705256.1:c.908A= ENSP00000516107.1:p.Asp303=
ENST00000366847.9:c.911A= MANE Select ENSP00000355812.3:p.Asp304=
ENST00000349556.4:c.851A= ENSP00000230248.6:p.Asp284=
ENST00000366847.8:c.911A= ENSP00000355812.3:p.Asp304=
ENST00000488525.1:n.97A=
ENST00000496181.1:n.315A=
ENST00000622353.4:c.770A= ENSP00000479115.1:p.Asp257=
NM_001278690.1:c.770A= NP_001265619.1:p.Asp257=
NM_007045.3:c.911A= NP_008976.1:p.Asp304=
NM_194429.2:c.851A= NP_919410.1:p.Asp284=
NM_007045.4:c.911A= MANE Select NP_008976.1:p.Asp304=
NM_194429.3:c.851A= NP_919410.1:p.Asp284=
NM_001278690.2:c.770A= NP_001265619.1:p.Asp257=