Canonical Allele Identifier: CA453081415

Gene: CEP43

Linked Data

• MyVariant Identifiers: chr6:g.167438303G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167024815G>A , CM000668.2:g.167024815G>A	GRCh38
NC_000006.11:g.167438303G>A , CM000668.1:g.167438303G>A	GRCh37
NC_000006.10:g.167358293G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349556.5:c.780G>A	ENSP00000230248.6:p.Leu260=
ENST00000488525.2:c.836G>A	ENSP00000516042.1:p.Trp279Ter
ENST00000609590.2:n.1712G>A
ENST00000704900.1:c.417G>A	ENSP00000516059.1:p.Leu139=
ENST00000704901.1:c.*427G>A	ENSP00000516060.1:n.*427G>A
ENST00000704959.1:n.1105G>A
ENST00000704982.1:n.1550G>A
ENST00000704985.1:n.1946G>A
ENST00000704986.1:n.1946G>A
ENST00000705029.1:n.1671G>A
ENST00000705059.1:n.1495G>A
ENST00000705168.1:c.93G>A	ENSP00000516071.1:p.Leu31=
ENST00000705169.1:c.93G>A	ENSP00000516072.1:p.Leu31=
ENST00000705170.1:c.93G>A	ENSP00000516073.1:p.Leu31=
ENST00000705171.1:n.885G>A
ENST00000705173.1:c.*149G>A	ENSP00000516075.1:n.*149G>A
ENST00000705175.1:c.966G>A	ENSP00000516077.1:p.Leu322=
ENST00000705176.1:c.1026G>A	ENSP00000516078.1:p.Leu342=
ENST00000705177.1:c.*424G>A	ENSP00000516079.1:n.*424G>A
ENST00000705178.1:c.363G>A	ENSP00000516080.1:p.Leu121=
ENST00000705179.1:c.558G>A	ENSP00000516081.1:p.Leu186=
ENST00000705180.1:c.498G>A	ENSP00000516082.1:p.Leu166=
ENST00000705235.1:c.840G>A	ENSP00000516093.1:p.Leu280=
ENST00000705236.1:c.780G>A	ENSP00000516094.1:p.Leu260=
ENST00000705237.1:c.498G>A	ENSP00000516095.1:p.Leu166=
ENST00000705238.1:c.699G>A	ENSP00000516096.1:p.Leu233=
ENST00000705239.1:c.777G>A	ENSP00000516097.1:p.Leu259=
ENST00000705240.1:c.*449G>A	ENSP00000516098.1:n.*449G>A
ENST00000705241.1:c.776G>A	ENSP00000516099.1:p.Trp259Ter
ENST00000705242.1:c.777G>A	ENSP00000516100.1:p.Leu259=
ENST00000705249.1:c.780G>A	ENSP00000516101.1:p.Leu260=
ENST00000705250.1:c.558G>A	ENSP00000516102.1:p.Leu186=
ENST00000705251.1:c.*427G>A	ENSP00000516103.1:n.*427G>A
ENST00000705252.1:c.*250G>A	ENSP00000516104.1:n.*250G>A
ENST00000705253.1:c.*250G>A	ENSP00000516105.1:n.*250G>A
ENST00000705254.1:c.387G>A	ENSP00000516106.1:p.Leu129=
ENST00000705255.1:n.1406G>A
ENST00000705256.1:c.837G>A	ENSP00000516107.1:p.Leu279=
ENST00000366847.9:c.840G>A MANE Select	ENSP00000355812.3:p.Leu280=
ENST00000349556.4:c.780G>A	ENSP00000230248.6:p.Leu260=
ENST00000366847.8:c.840G>A	ENSP00000355812.3:p.Leu280=
ENST00000488525.1:n.26G>A
ENST00000496181.1:n.244G>A
ENST00000622353.4:c.699G>A	ENSP00000479115.1:p.Leu233=
NM_001278690.1:c.699G>A	NP_001265619.1:p.Leu233=
NM_007045.3:c.840G>A	NP_008976.1:p.Leu280=
NM_194429.2:c.780G>A	NP_919410.1:p.Leu260=
NM_007045.4:c.840G>A MANE Select	NP_008976.1:p.Leu280=
NM_194429.3:c.780G>A	NP_919410.1:p.Leu260=
NM_001278690.2:c.699G>A	NP_001265619.1:p.Leu233=