Canonical Allele Identifier: CA353876310
Gene: CEP97 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101757721T>C , CM000665.2:g.101757721T>C GRCh38
NC_000003.11:g.101476565T>C , CM000665.1:g.101476565T>C GRCh37
NC_000003.10:g.102959255T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*750T>C ENSP00000419009.1:n.*750T>C
ENST00000467655.2:c.*202T>C ENSP00000418547.2:n.*202T>C
ENST00000704365.1:c.1115T>C ENSP00000515873.1:p.Val372Ala
ENST00000704366.1:c.1013T>C ENSP00000515874.1:p.Val338Ala
ENST00000704367.1:c.926-90T>C ENSP00000515875.1:n.926-90T>C
ENST00000704368.1:n.1608T>C
ENST00000704369.1:c.629T>C ENSP00000515876.1:p.Val210Ala
ENST00000704370.1:c.1109T>C ENSP00000515877.1:p.Val370Ala
ENST00000704372.1:n.1469T>C
ENST00000704444.1:c.899T>C ENSP00000515896.1:p.Val300Ala
ENST00000704445.1:c.767T>C ENSP00000515897.1:p.Val256Ala
ENST00000704446.1:c.1048+525T>C ENSP00000515898.1:n.1048+525T>C
ENST00000341893.8:c.1115T>C MANE Select ENSP00000342510.3:p.Val372Ala
ENST00000341893.7:c.1115T>C ENSP00000342510.3:p.Val372Ala
ENST00000467655.1:c.730T>C ENSP00000418547.1:n.730T>C
ENST00000489172.5:n.1097T>C
ENST00000494050.5:c.1028-90T>C ENSP00000418185.1:n.1028-90T>C
NM_001303401.1:c.1028-90T>C NP_001290330.1:n.1028-90T>C
NM_024548.3:c.1115T>C NP_078824.2:p.Val372Ala
XM_006713743.2:c.1013T>C XP_006713806.1:p.Val338Ala
XM_011513125.1:c.899T>C XP_011511427.1:p.Val300Ala
XM_011513126.1:c.899T>C XP_011511428.1:p.Val300Ala
XM_011513127.1:c.767T>C XP_011511429.1:p.Val256Ala
XM_006713743.4:c.1013T>C XP_006713806.1:p.Val338Ala
XM_017007178.2:c.926-90T>C XP_016862667.1:n.926-90T>C
NM_024548.4:c.1115T>C MANE Select NP_078824.2:p.Val372Ala
NM_001303401.2:c.1028-90T>C NP_001290330.1:n.1028-90T>C