Canonical Allele Identifier: CA1388867455

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757864G= , CM000665.2:g.101757864G=	GRCh38
NC_000003.11:g.101476708G= , CM000665.1:g.101476708G=	GRCh37
NC_000003.10:g.102959398G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*893G=	ENSP00000419009.1:n.*893G=
ENST00000467655.2:c.*345G=	ENSP00000418547.2:n.*345G=
ENST00000704365.1:c.1258G=	ENSP00000515873.1:p.Glu420=
ENST00000704366.1:c.1156G=	ENSP00000515874.1:p.Glu386=
ENST00000704367.1:c.979G=	ENSP00000515875.1:p.Glu327=
ENST00000704368.1:n.1751G=
ENST00000704369.1:c.772G=	ENSP00000515876.1:p.Glu258=
ENST00000704370.1:c.1252G=	ENSP00000515877.1:p.Glu418=
ENST00000704372.1:n.1612G=
ENST00000704444.1:c.1042G=	ENSP00000515896.1:p.Glu348=
ENST00000704445.1:c.910G=	ENSP00000515897.1:p.Glu304=
ENST00000704446.1:c.1048+668G=	ENSP00000515898.1:n.1048+668G=
ENST00000341893.8:c.1258G= MANE Select	ENSP00000342510.3:p.Glu420=
ENST00000341893.7:c.1258G=	ENSP00000342510.3:p.Glu420=
ENST00000467655.1:c.873G=	ENSP00000418547.1:n.873G=
ENST00000489172.5:n.1240G=
ENST00000494050.5:c.1081G=	ENSP00000418185.1:p.Glu361=
NM_001303401.1:c.1081G=	NP_001290330.1:p.Glu361=
NM_024548.3:c.1258G=	NP_078824.2:p.Glu420=
XM_006713743.2:c.1156G=	XP_006713806.1:p.Glu386=
XM_011513125.1:c.1042G=	XP_011511427.1:p.Glu348=
XM_011513126.1:c.1042G=	XP_011511428.1:p.Glu348=
XM_011513127.1:c.910G=	XP_011511429.1:p.Glu304=
XM_006713743.4:c.1156G=	XP_006713806.1:p.Glu386=
XM_017007178.2:c.979G=	XP_016862667.1:p.Glu327=
NM_024548.4:c.1258G= MANE Select	NP_078824.2:p.Glu420=
NM_001303401.2:c.1081G=	NP_001290330.1:p.Glu361=