Canonical Allele Identifier: CA1388867411

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757772C= , CM000665.2:g.101757772C=	GRCh38
NC_000003.11:g.101476616C= , CM000665.1:g.101476616C=	GRCh37
NC_000003.10:g.102959306C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*801C=	ENSP00000419009.1:n.*801C=
ENST00000467655.2:c.*253C=	ENSP00000418547.2:n.*253C=
ENST00000704365.1:c.1166C=	ENSP00000515873.1:p.Thr389=
ENST00000704366.1:c.1064C=	ENSP00000515874.1:p.Thr355=
ENST00000704367.1:c.926-39C=	ENSP00000515875.1:n.926-39C=
ENST00000704368.1:n.1659C=
ENST00000704369.1:c.680C=	ENSP00000515876.1:p.Thr227=
ENST00000704370.1:c.1160C=	ENSP00000515877.1:p.Thr387=
ENST00000704372.1:n.1520C=
ENST00000704444.1:c.950C=	ENSP00000515896.1:p.Thr317=
ENST00000704445.1:c.818C=	ENSP00000515897.1:p.Thr273=
ENST00000704446.1:c.1048+576C=	ENSP00000515898.1:n.1048+576C=
ENST00000341893.8:c.1166C= MANE Select	ENSP00000342510.3:p.Thr389=
ENST00000341893.7:c.1166C=	ENSP00000342510.3:p.Thr389=
ENST00000467655.1:c.781C=	ENSP00000418547.1:n.781C=
ENST00000489172.5:n.1148C=
ENST00000494050.5:c.1028-39C=	ENSP00000418185.1:n.1028-39C=
NM_001303401.1:c.1028-39C=	NP_001290330.1:n.1028-39C=
NM_024548.3:c.1166C=	NP_078824.2:p.Thr389=
XM_006713743.2:c.1064C=	XP_006713806.1:p.Thr355=
XM_011513125.1:c.950C=	XP_011511427.1:p.Thr317=
XM_011513126.1:c.950C=	XP_011511428.1:p.Thr317=
XM_011513127.1:c.818C=	XP_011511429.1:p.Thr273=
XM_006713743.4:c.1064C=	XP_006713806.1:p.Thr355=
XM_017007178.2:c.926-39C=	XP_016862667.1:n.926-39C=
NM_024548.4:c.1166C= MANE Select	NP_078824.2:p.Thr389=
NM_001303401.2:c.1028-39C=	NP_001290330.1:n.1028-39C=