Canonical Allele Identifier: CA353877577
Gene: CEP97 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101758038A>G , CM000665.2:g.101758038A>G GRCh38
NC_000003.11:g.101476882A>G , CM000665.1:g.101476882A>G GRCh37
NC_000003.10:g.102959572A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*1067A>G ENSP00000419009.1:n.*1067A>G
ENST00000467655.2:c.*519A>G ENSP00000418547.2:n.*519A>G
ENST00000704365.1:c.1432A>G ENSP00000515873.1:p.Lys478Glu
ENST00000704366.1:c.1330A>G ENSP00000515874.1:p.Lys444Glu
ENST00000704367.1:c.1153A>G ENSP00000515875.1:p.Lys385Glu
ENST00000704368.1:n.1925A>G
ENST00000704369.1:c.946A>G ENSP00000515876.1:p.Lys316Glu
ENST00000704370.1:c.1426A>G ENSP00000515877.1:p.Lys476Glu
ENST00000704372.1:n.1786A>G
ENST00000704444.1:c.1216A>G ENSP00000515896.1:p.Lys406Glu
ENST00000704445.1:c.1084A>G ENSP00000515897.1:p.Lys362Glu
ENST00000704446.1:c.1048+842A>G ENSP00000515898.1:n.1048+842A>G
ENST00000341893.8:c.1432A>G MANE Select ENSP00000342510.3:p.Lys478Glu
ENST00000341893.7:c.1432A>G ENSP00000342510.3:p.Lys478Glu
ENST00000467655.1:c.1047A>G ENSP00000418547.1:n.1047A>G
ENST00000489172.5:n.1414A>G
ENST00000494050.5:c.1255A>G ENSP00000418185.1:p.Lys419Glu
NM_001303401.1:c.1255A>G NP_001290330.1:p.Lys419Glu
NM_024548.3:c.1432A>G NP_078824.2:p.Lys478Glu
XM_006713743.2:c.1330A>G XP_006713806.1:p.Lys444Glu
XM_011513125.1:c.1216A>G XP_011511427.1:p.Lys406Glu
XM_011513126.1:c.1216A>G XP_011511428.1:p.Lys406Glu
XM_011513127.1:c.1084A>G XP_011511429.1:p.Lys362Glu
XM_006713743.4:c.1330A>G XP_006713806.1:p.Lys444Glu
XM_017007178.2:c.1153A>G XP_016862667.1:p.Lys385Glu
NM_024548.4:c.1432A>G MANE Select NP_078824.2:p.Lys478Glu
NM_001303401.2:c.1255A>G NP_001290330.1:p.Lys419Glu