Canonical Allele Identifier: CA353876552

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476604A>T (hg19) ; chr3:g.101757760A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757760A>T , CM000665.2:g.101757760A>T	GRCh38
NC_000003.11:g.101476604A>T , CM000665.1:g.101476604A>T	GRCh37
NC_000003.10:g.102959294A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000465011.2:c.*789A>T	ENSP00000419009.1:n.*789A>T
ENST00000467655.2:c.*241A>T	ENSP00000418547.2:n.*241A>T
ENST00000704365.1:c.1154A>T	ENSP00000515873.1:p.Glu385Val
ENST00000704366.1:c.1052A>T	ENSP00000515874.1:p.Glu351Val
ENST00000704367.1:c.926-51A>T	ENSP00000515875.1:n.926-51A>T
ENST00000704368.1:n.1647A>T
ENST00000704369.1:c.668A>T	ENSP00000515876.1:p.Glu223Val
ENST00000704370.1:c.1148A>T	ENSP00000515877.1:p.Glu383Val
ENST00000704372.1:n.1508A>T
ENST00000704444.1:c.938A>T	ENSP00000515896.1:p.Glu313Val
ENST00000704445.1:c.806A>T	ENSP00000515897.1:p.Glu269Val
ENST00000704446.1:c.1048+564A>T	ENSP00000515898.1:n.1048+564A>T
ENST00000341893.8:c.1154A>T MANE Select	ENSP00000342510.3:p.Glu385Val
ENST00000341893.7:c.1154A>T	ENSP00000342510.3:p.Glu385Val
ENST00000467655.1:c.769A>T	ENSP00000418547.1:n.769A>T
ENST00000489172.5:n.1136A>T
ENST00000494050.5:c.1028-51A>T	ENSP00000418185.1:n.1028-51A>T
NM_001303401.1:c.1028-51A>T	NP_001290330.1:n.1028-51A>T
NM_024548.3:c.1154A>T	NP_078824.2:p.Glu385Val
XM_006713743.2:c.1052A>T	XP_006713806.1:p.Glu351Val
XM_011513125.1:c.938A>T	XP_011511427.1:p.Glu313Val
XM_011513126.1:c.938A>T	XP_011511428.1:p.Glu313Val
XM_011513127.1:c.806A>T	XP_011511429.1:p.Glu269Val
XM_006713743.4:c.1052A>T	XP_006713806.1:p.Glu351Val
XM_017007178.2:c.926-51A>T	XP_016862667.1:n.926-51A>T
NM_024548.4:c.1154A>T MANE Select	NP_078824.2:p.Glu385Val
NM_001303401.2:c.1028-51A>T	NP_001290330.1:n.1028-51A>T