Canonical Allele Identifier: CA392358126
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 517617
dbSNP Id: rs1342429887

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48797527C>T , CM000677.2:g.48797527C>T GRCh38
NC_000015.9:g.49089724C>T , CM000677.1:g.49089724C>T GRCh37
NC_000015.8:g.46877016C>T NCBI36
NG_027518.1:g.18620G>A
NG_027518.2:g.18620G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380950.7:c.314G>A MANE Select ENSP00000370337.2:p.Trp105Ter
ENST00000325747.9:c.261+134G>A ENSP00000321000.5:n.261+134G>A
ENST00000380950.6:c.314G>A ENSP00000370337.2:p.Trp105Ter
ENST00000399334.7:c.314G>A ENSP00000382271.3:p.Trp105Ter
ENST00000560322.5:c.314G>A ENSP00000453440.1:p.Trp105Ter
NM_001194998.1:c.314G>A NP_001181927.1:p.Trp105Ter
NM_014985.3:c.314G>A NP_055800.2:p.Trp105Ter
XM_006720437.2:c.314G>A XP_006720500.1:p.Trp105Ter
XM_011521373.1:c.314G>A XP_011519675.1:p.Trp105Ter
XM_011521374.1:c.314G>A XP_011519676.1:p.Trp105Ter
XM_011521375.1:c.314G>A XP_011519677.1:p.Trp105Ter
XM_011521376.1:c.314G>A XP_011519678.1:p.Trp105Ter
XM_011521377.1:c.314G>A XP_011519679.1:p.Trp105Ter
XM_011521378.1:c.314G>A XP_011519680.1:p.Trp105Ter
XM_011521379.1:c.314G>A XP_011519681.1:p.Trp105Ter
XR_931769.1:n.1279G>A
XR_931770.1:n.1279G>A
XR_931771.1:n.1279G>A
XR_931772.1:n.1279G>A
XR_931773.1:n.1279G>A
XR_931774.1:n.1279G>A
XR_931775.1:n.1279G>A
XM_006720437.3:c.314G>A XP_006720500.1:p.Trp105Ter
XM_011521373.3:c.314G>A XP_011519675.1:p.Trp105Ter
XM_011521374.3:c.314G>A XP_011519676.1:p.Trp105Ter
XM_011521375.3:c.314G>A XP_011519677.1:p.Trp105Ter
XM_011521378.3:c.314G>A XP_011519680.1:p.Trp105Ter
XM_011521379.3:c.314G>A XP_011519681.1:p.Trp105Ter
XM_017022016.2:c.314G>A XP_016877505.1:p.Trp105Ter
XM_024449875.1:c.314G>A XP_024305643.1:p.Trp105Ter
XR_001751153.2:n.1265G>A
XR_931769.3:n.1265G>A
XR_931770.3:n.1265G>A
XR_931775.3:n.1265G>A
NM_001194998.2:c.314G>A MANE Select NP_001181927.1:p.Trp105Ter
NM_014985.4:c.314G>A NP_055800.2:p.Trp105Ter