Canonical Allele Identifier: CA822254949

Gene: CEP43

Linked Data

• dbSNP Id: rs1354303712
• gnomAD v3: 6-167024371-A-AG
• gnomAD v4: 6-167024371-A-AG
• MyVariant Identifiers: chr6:g.167437859_167437860insG (hg19) ; chr6:g.167024371_167024372insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167024375dup , CM000668.2:g.167024375dup	GRCh38
NC_000006.11:g.167437863dup , CM000668.1:g.167437863dup	GRCh37
NC_000006.10:g.167357853dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000349556.5:c.747-407dup	ENSP00000230248.6:n.747-407dup
ENST00000488525.2:c.803-407dup	ENSP00000516042.1:n.803-407dup
ENST00000609590.2:n.1682-410dup
ENST00000704900.1:c.384-407dup	ENSP00000516059.1:n.384-407dup
ENST00000704901.1:c.*394-407dup	ENSP00000516060.1:n.*394-407dup
ENST00000704959.1:n.1072-407dup
ENST00000704982.1:n.1517-407dup
ENST00000704985.1:n.1913-407dup
ENST00000704986.1:n.1913-407dup
ENST00000705029.1:n.1231dup
ENST00000705059.1:n.1462-407dup
ENST00000705168.1:c.60-407dup	ENSP00000516071.1:n.60-407dup
ENST00000705169.1:c.60-407dup	ENSP00000516072.1:n.60-407dup
ENST00000705170.1:c.60-407dup	ENSP00000516073.1:n.60-407dup
ENST00000705171.1:n.852-407dup
ENST00000705173.1:c.*116-407dup	ENSP00000516075.1:n.*116-407dup
ENST00000705175.1:c.933-407dup	ENSP00000516077.1:n.933-407dup
ENST00000705176.1:c.993-407dup	ENSP00000516078.1:n.993-407dup
ENST00000705177.1:c.*391-407dup	ENSP00000516079.1:n.*391-407dup
ENST00000705178.1:c.330-407dup	ENSP00000516080.1:n.330-407dup
ENST00000705179.1:c.525-407dup	ENSP00000516081.1:n.525-407dup
ENST00000705180.1:c.465-407dup	ENSP00000516082.1:n.465-407dup
ENST00000705235.1:c.807-407dup	ENSP00000516093.1:n.807-407dup
ENST00000705236.1:c.747-407dup	ENSP00000516094.1:n.747-407dup
ENST00000705237.1:c.465-407dup	ENSP00000516095.1:n.465-407dup
ENST00000705238.1:c.666-407dup	ENSP00000516096.1:n.666-407dup
ENST00000705239.1:c.747-410dup	ENSP00000516097.1:n.747-410dup
ENST00000705240.1:c.*416-407dup	ENSP00000516098.1:n.*416-407dup
ENST00000705241.1:c.743-407dup	ENSP00000516099.1:n.743-407dup
ENST00000705242.1:c.744-407dup	ENSP00000516100.1:n.744-407dup
ENST00000705249.1:c.747-407dup	ENSP00000516101.1:n.747-407dup
ENST00000705250.1:c.525-407dup	ENSP00000516102.1:n.525-407dup
ENST00000705251.1:c.*394-407dup	ENSP00000516103.1:n.*394-407dup
ENST00000705252.1:c.*217-407dup	ENSP00000516104.1:n.*217-407dup
ENST00000705253.1:c.*217-407dup	ENSP00000516105.1:n.*217-407dup
ENST00000705254.1:c.354-407dup	ENSP00000516106.1:n.354-407dup
ENST00000705255.1:n.1373-407dup
ENST00000705256.1:c.807-410dup	ENSP00000516107.1:n.807-410dup
ENST00000366847.9:c.807-407dup MANE Select	ENSP00000355812.3:n.807-407dup
ENST00000349556.4:c.747-407dup	ENSP00000230248.6:n.747-407dup
ENST00000366847.8:c.807-407dup	ENSP00000355812.3:n.807-407dup
ENST00000496181.1:n.211-407dup
ENST00000622353.4:c.666-407dup	ENSP00000479115.1:n.666-407dup
NM_001278690.1:c.666-407dup	NP_001265619.1:n.666-407dup
NM_007045.3:c.807-407dup	NP_008976.1:n.807-407dup
NM_194429.2:c.747-407dup	NP_919410.1:n.747-407dup
NM_007045.4:c.807-407dup MANE Select	NP_008976.1:n.807-407dup
NM_194429.3:c.747-407dup	NP_919410.1:n.747-407dup
NM_001278690.2:c.666-407dup	NP_001265619.1:n.666-407dup