Canonical Allele Identifier: CA353877834
Gene: CEP97 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101758153A>G , CM000665.2:g.101758153A>G GRCh38
NC_000003.11:g.101476997A>G , CM000665.1:g.101476997A>G GRCh37
NC_000003.10:g.102959687A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*1182A>G ENSP00000419009.1:n.*1182A>G
ENST00000467655.2:c.*634A>G ENSP00000418547.2:n.*634A>G
ENST00000704365.1:c.1547A>G ENSP00000515873.1:p.Lys516Arg
ENST00000704366.1:c.1445A>G ENSP00000515874.1:p.Lys482Arg
ENST00000704367.1:c.1268A>G ENSP00000515875.1:p.Lys423Arg
ENST00000704368.1:n.2040A>G
ENST00000704369.1:c.1061A>G ENSP00000515876.1:p.Lys354Arg
ENST00000704370.1:c.1541A>G ENSP00000515877.1:p.Lys514Arg
ENST00000704372.1:n.1901A>G
ENST00000704444.1:c.1331A>G ENSP00000515896.1:p.Lys444Arg
ENST00000704445.1:c.1199A>G ENSP00000515897.1:p.Lys400Arg
ENST00000704446.1:c.1048+957A>G ENSP00000515898.1:n.1048+957A>G
ENST00000341893.8:c.1547A>G MANE Select ENSP00000342510.3:p.Lys516Arg
ENST00000341893.7:c.1547A>G ENSP00000342510.3:p.Lys516Arg
ENST00000467655.1:c.1162A>G ENSP00000418547.1:n.1162A>G
ENST00000489172.5:n.1529A>G
ENST00000494050.5:c.1370A>G ENSP00000418185.1:p.Lys457Arg
NM_001303401.1:c.1370A>G NP_001290330.1:p.Lys457Arg
NM_024548.3:c.1547A>G NP_078824.2:p.Lys516Arg
XM_006713743.2:c.1445A>G XP_006713806.1:p.Lys482Arg
XM_011513125.1:c.1331A>G XP_011511427.1:p.Lys444Arg
XM_011513126.1:c.1331A>G XP_011511428.1:p.Lys444Arg
XM_011513127.1:c.1199A>G XP_011511429.1:p.Lys400Arg
XM_006713743.4:c.1445A>G XP_006713806.1:p.Lys482Arg
XM_017007178.2:c.1268A>G XP_016862667.1:p.Lys423Arg
NM_024548.4:c.1547A>G MANE Select NP_078824.2:p.Lys516Arg
NM_001303401.2:c.1370A>G NP_001290330.1:p.Lys457Arg