Canonical Allele Identifier: CA353877838
Gene: CEP97 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101758155A>G , CM000665.2:g.101758155A>G GRCh38
NC_000003.11:g.101476999A>G , CM000665.1:g.101476999A>G GRCh37
NC_000003.10:g.102959689A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*1184A>G ENSP00000419009.1:n.*1184A>G
ENST00000467655.2:c.*636A>G ENSP00000418547.2:n.*636A>G
ENST00000704365.1:c.1549A>G ENSP00000515873.1:p.Lys517Glu
ENST00000704366.1:c.1447A>G ENSP00000515874.1:p.Lys483Glu
ENST00000704367.1:c.1270A>G ENSP00000515875.1:p.Lys424Glu
ENST00000704368.1:n.2042A>G
ENST00000704369.1:c.1063A>G ENSP00000515876.1:p.Lys355Glu
ENST00000704370.1:c.1543A>G ENSP00000515877.1:p.Lys515Glu
ENST00000704372.1:n.1903A>G
ENST00000704444.1:c.1333A>G ENSP00000515896.1:p.Lys445Glu
ENST00000704445.1:c.1201A>G ENSP00000515897.1:p.Lys401Glu
ENST00000704446.1:c.1048+959A>G ENSP00000515898.1:n.1048+959A>G
ENST00000341893.8:c.1549A>G MANE Select ENSP00000342510.3:p.Lys517Glu
ENST00000341893.7:c.1549A>G ENSP00000342510.3:p.Lys517Glu
ENST00000467655.1:c.1164A>G ENSP00000418547.1:n.1164A>G
ENST00000489172.5:n.1531A>G
ENST00000494050.5:c.1372A>G ENSP00000418185.1:p.Lys458Glu
NM_001303401.1:c.1372A>G NP_001290330.1:p.Lys458Glu
NM_024548.3:c.1549A>G NP_078824.2:p.Lys517Glu
XM_006713743.2:c.1447A>G XP_006713806.1:p.Lys483Glu
XM_011513125.1:c.1333A>G XP_011511427.1:p.Lys445Glu
XM_011513126.1:c.1333A>G XP_011511428.1:p.Lys445Glu
XM_011513127.1:c.1201A>G XP_011511429.1:p.Lys401Glu
XM_006713743.4:c.1447A>G XP_006713806.1:p.Lys483Glu
XM_017007178.2:c.1270A>G XP_016862667.1:p.Lys424Glu
NM_024548.4:c.1549A>G MANE Select NP_078824.2:p.Lys517Glu
NM_001303401.2:c.1372A>G NP_001290330.1:p.Lys458Glu