Canonical Allele Identifier: CA353877841
Gene: CEP97 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101758156A>C , CM000665.2:g.101758156A>C GRCh38
NC_000003.11:g.101477000A>C , CM000665.1:g.101477000A>C GRCh37
NC_000003.10:g.102959690A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*1185A>C ENSP00000419009.1:n.*1185A>C
ENST00000467655.2:c.*637A>C ENSP00000418547.2:n.*637A>C
ENST00000704365.1:c.1550A>C ENSP00000515873.1:p.Lys517Thr
ENST00000704366.1:c.1448A>C ENSP00000515874.1:p.Lys483Thr
ENST00000704367.1:c.1271A>C ENSP00000515875.1:p.Lys424Thr
ENST00000704368.1:n.2043A>C
ENST00000704369.1:c.1064A>C ENSP00000515876.1:p.Lys355Thr
ENST00000704370.1:c.1544A>C ENSP00000515877.1:p.Lys515Thr
ENST00000704372.1:n.1904A>C
ENST00000704444.1:c.1334A>C ENSP00000515896.1:p.Lys445Thr
ENST00000704445.1:c.1202A>C ENSP00000515897.1:p.Lys401Thr
ENST00000704446.1:c.1048+960A>C ENSP00000515898.1:n.1048+960A>C
ENST00000341893.8:c.1550A>C MANE Select ENSP00000342510.3:p.Lys517Thr
ENST00000341893.7:c.1550A>C ENSP00000342510.3:p.Lys517Thr
ENST00000467655.1:c.1165A>C ENSP00000418547.1:n.1165A>C
ENST00000489172.5:n.1532A>C
ENST00000494050.5:c.1373A>C ENSP00000418185.1:p.Lys458Thr
NM_001303401.1:c.1373A>C NP_001290330.1:p.Lys458Thr
NM_024548.3:c.1550A>C NP_078824.2:p.Lys517Thr
XM_006713743.2:c.1448A>C XP_006713806.1:p.Lys483Thr
XM_011513125.1:c.1334A>C XP_011511427.1:p.Lys445Thr
XM_011513126.1:c.1334A>C XP_011511428.1:p.Lys445Thr
XM_011513127.1:c.1202A>C XP_011511429.1:p.Lys401Thr
XM_006713743.4:c.1448A>C XP_006713806.1:p.Lys483Thr
XM_017007178.2:c.1271A>C XP_016862667.1:p.Lys424Thr
NM_024548.4:c.1550A>C MANE Select NP_078824.2:p.Lys517Thr
NM_001303401.2:c.1373A>C NP_001290330.1:p.Lys458Thr