Canonical Allele Identifier: CA293490629
Gene: CEP112 HGNC NCBI

Linked Data

dbSNP Id: rs7209395

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66137608T>C , CM000679.2:g.66137608T>C GRCh38
NC_000017.10:g.64133726T>C , CM000679.1:g.64133726T>C GRCh37
NC_000017.9:g.61564188T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706790.1:c.471-4845A>G ENSP00000516553.1:n.471-4845A>G
ENST00000706791.1:c.107-4845A>G ENSP00000516554.1:n.107-4845A>G
ENST00000706792.1:c.402-4845A>G ENSP00000516555.1:n.402-4845A>G
ENST00000706793.1:c.471-4845A>G ENSP00000516556.1:n.471-4845A>G
ENST00000706794.1:c.470+37436A>G ENSP00000516557.1:n.470+37436A>G
ENST00000706795.1:c.471-4845A>G ENSP00000516558.1:n.471-4845A>G
ENST00000706796.1:n.600-4845A>G
ENST00000706799.1:n.726-4845A>G
ENST00000535342.7:c.471-4845A>G MANE Select ENSP00000442784.2:n.471-4845A>G
ENST00000392769.6:c.471-4845A>G ENSP00000376522.2:n.471-4845A>G
ENST00000535342.6:c.471-4845A>G ENSP00000442784.2:n.471-4845A>G
ENST00000537949.5:c.471-4845A>G ENSP00000440775.1:n.471-4845A>G
ENST00000583358.1:c.471-4845A>G ENSP00000463914.1:n.471-4845A>G
NM_001199165.2:c.471-4845A>G NP_001186094.1:n.471-4845A>G
NM_001302891.1:c.471-4845A>G NP_001289820.1:n.471-4845A>G
XM_005257119.3:c.471-4845A>G XP_005257176.1:n.471-4845A>G
XM_006721740.2:c.471-4845A>G XP_006721803.1:n.471-4845A>G
XM_006721741.2:c.471-4845A>G XP_006721804.1:n.471-4845A>G
XM_006721742.2:c.471-4845A>G XP_006721805.1:n.471-4845A>G
XM_006721744.2:c.471-4845A>G XP_006721807.1:n.471-4845A>G
XM_011524461.1:c.471-4845A>G XP_011522763.1:n.471-4845A>G
XM_011524462.1:c.471-4845A>G XP_011522764.1:n.471-4845A>G
XM_011524463.1:c.471-4845A>G XP_011522765.1:n.471-4845A>G
XM_011524464.1:c.471-4845A>G XP_011522766.1:n.471-4845A>G
XM_011524465.1:c.-224+1878A>G XP_011522767.1:n.-224+1878A>G
XR_934412.1:n.704-4845A>G
XR_934413.1:n.709-4845A>G
XR_934414.1:n.708-4845A>G
NM_001199165.3:c.471-4845A>G NP_001186094.1:n.471-4845A>G
NM_001302891.2:c.471-4845A>G NP_001289820.1:n.471-4845A>G
NM_001353127.1:c.471-4845A>G NP_001340056.1:n.471-4845A>G
NM_001353128.1:c.471-4845A>G NP_001340057.1:n.471-4845A>G
NM_001353129.1:c.471-4845A>G NP_001340058.1:n.471-4845A>G
XM_005257119.5:c.471-4845A>G XP_005257176.1:n.471-4845A>G
XM_006721744.3:c.471-4845A>G XP_006721807.1:n.471-4845A>G
XM_011524462.3:c.471-4845A>G XP_011522764.1:n.471-4845A>G
XM_011524463.2:c.471-4845A>G XP_011522765.1:n.471-4845A>G
XM_011524464.3:c.471-4845A>G XP_011522766.1:n.471-4845A>G
XM_011524465.2:c.-224+1878A>G XP_011522767.1:n.-224+1878A>G
XM_024450634.1:c.-221+1878A>G XP_024306402.1:n.-221+1878A>G
XR_001752444.1:n.709-4845A>G
XR_934412.2:n.707-4845A>G
XR_934414.2:n.709-4845A>G
NM_001199165.4:c.471-4845A>G MANE Select NP_001186094.1:n.471-4845A>G
NM_001302891.3:c.471-4845A>G NP_001289820.1:n.471-4845A>G
NM_001353128.2:c.471-4845A>G NP_001340057.1:n.471-4845A>G
NM_001353129.2:c.471-4845A>G NP_001340058.1:n.471-4845A>G
NM_001353127.2:c.471-4845A>G NP_001340056.1:n.471-4845A>G