Canonical Allele Identifier: CA2544934925

Gene: CEP43

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167024423T>G , CM000668.2:g.167024423T>G	GRCh38
NC_000006.11:g.167437911T>G , CM000668.1:g.167437911T>G	GRCh37
NC_000006.10:g.167357901T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000349556.5:c.747-359T>G	ENSP00000230248.6:n.747-359T>G
ENST00000488525.2:c.803-359T>G	ENSP00000516042.1:n.803-359T>G
ENST00000609590.2:n.1682-362T>G
ENST00000704900.1:c.384-359T>G	ENSP00000516059.1:n.384-359T>G
ENST00000704901.1:c.*394-359T>G	ENSP00000516060.1:n.*394-359T>G
ENST00000704959.1:n.1072-359T>G
ENST00000704982.1:n.1517-359T>G
ENST00000704985.1:n.1913-359T>G
ENST00000704986.1:n.1913-359T>G
ENST00000705029.1:n.1279T>G
ENST00000705059.1:n.1462-359T>G
ENST00000705168.1:c.60-359T>G	ENSP00000516071.1:n.60-359T>G
ENST00000705169.1:c.60-359T>G	ENSP00000516072.1:n.60-359T>G
ENST00000705170.1:c.60-359T>G	ENSP00000516073.1:n.60-359T>G
ENST00000705171.1:n.852-359T>G
ENST00000705173.1:c.*116-359T>G	ENSP00000516075.1:n.*116-359T>G
ENST00000705175.1:c.933-359T>G	ENSP00000516077.1:n.933-359T>G
ENST00000705176.1:c.993-359T>G	ENSP00000516078.1:n.993-359T>G
ENST00000705177.1:c.*391-359T>G	ENSP00000516079.1:n.*391-359T>G
ENST00000705178.1:c.330-359T>G	ENSP00000516080.1:n.330-359T>G
ENST00000705179.1:c.525-359T>G	ENSP00000516081.1:n.525-359T>G
ENST00000705180.1:c.465-359T>G	ENSP00000516082.1:n.465-359T>G
ENST00000705235.1:c.807-359T>G	ENSP00000516093.1:n.807-359T>G
ENST00000705236.1:c.747-359T>G	ENSP00000516094.1:n.747-359T>G
ENST00000705237.1:c.465-359T>G	ENSP00000516095.1:n.465-359T>G
ENST00000705238.1:c.666-359T>G	ENSP00000516096.1:n.666-359T>G
ENST00000705239.1:c.747-362T>G	ENSP00000516097.1:n.747-362T>G
ENST00000705240.1:c.*416-359T>G	ENSP00000516098.1:n.*416-359T>G
ENST00000705241.1:c.743-359T>G	ENSP00000516099.1:n.743-359T>G
ENST00000705242.1:c.744-359T>G	ENSP00000516100.1:n.744-359T>G
ENST00000705249.1:c.747-359T>G	ENSP00000516101.1:n.747-359T>G
ENST00000705250.1:c.525-359T>G	ENSP00000516102.1:n.525-359T>G
ENST00000705251.1:c.*394-359T>G	ENSP00000516103.1:n.*394-359T>G
ENST00000705252.1:c.*217-359T>G	ENSP00000516104.1:n.*217-359T>G
ENST00000705253.1:c.*217-359T>G	ENSP00000516105.1:n.*217-359T>G
ENST00000705254.1:c.354-359T>G	ENSP00000516106.1:n.354-359T>G
ENST00000705255.1:n.1373-359T>G
ENST00000705256.1:c.807-362T>G	ENSP00000516107.1:n.807-362T>G
ENST00000366847.9:c.807-359T>G MANE Select	ENSP00000355812.3:n.807-359T>G
ENST00000349556.4:c.747-359T>G	ENSP00000230248.6:n.747-359T>G
ENST00000366847.8:c.807-359T>G	ENSP00000355812.3:n.807-359T>G
ENST00000496181.1:n.211-359T>G
ENST00000622353.4:c.666-359T>G	ENSP00000479115.1:n.666-359T>G
NM_001278690.1:c.666-359T>G	NP_001265619.1:n.666-359T>G
NM_007045.3:c.807-359T>G	NP_008976.1:n.807-359T>G
NM_194429.2:c.747-359T>G	NP_919410.1:n.747-359T>G
NM_007045.4:c.807-359T>G MANE Select	NP_008976.1:n.807-359T>G
NM_194429.3:c.747-359T>G	NP_919410.1:n.747-359T>G
NM_001278690.2:c.666-359T>G	NP_001265619.1:n.666-359T>G