Canonical Allele Identifier: CA1388867419

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757792T= , CM000665.2:g.101757792T=	GRCh38
NC_000003.11:g.101476636T= , CM000665.1:g.101476636T=	GRCh37
NC_000003.10:g.102959326T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*821T=	ENSP00000419009.1:n.*821T=
ENST00000467655.2:c.*273T=	ENSP00000418547.2:n.*273T=
ENST00000704365.1:c.1186T=	ENSP00000515873.1:p.Cys396=
ENST00000704366.1:c.1084T=	ENSP00000515874.1:p.Cys362=
ENST00000704367.1:c.926-19T=	ENSP00000515875.1:n.926-19T=
ENST00000704368.1:n.1679T=
ENST00000704369.1:c.700T=	ENSP00000515876.1:p.Cys234=
ENST00000704370.1:c.1180T=	ENSP00000515877.1:p.Cys394=
ENST00000704372.1:n.1540T=
ENST00000704444.1:c.970T=	ENSP00000515896.1:p.Cys324=
ENST00000704445.1:c.838T=	ENSP00000515897.1:p.Cys280=
ENST00000704446.1:c.1048+596T=	ENSP00000515898.1:n.1048+596T=
ENST00000341893.8:c.1186T= MANE Select	ENSP00000342510.3:p.Cys396=
ENST00000341893.7:c.1186T=	ENSP00000342510.3:p.Cys396=
ENST00000467655.1:c.801T=	ENSP00000418547.1:n.801T=
ENST00000489172.5:n.1168T=
ENST00000494050.5:c.1028-19T=	ENSP00000418185.1:n.1028-19T=
NM_001303401.1:c.1028-19T=	NP_001290330.1:n.1028-19T=
NM_024548.3:c.1186T=	NP_078824.2:p.Cys396=
XM_006713743.2:c.1084T=	XP_006713806.1:p.Cys362=
XM_011513125.1:c.970T=	XP_011511427.1:p.Cys324=
XM_011513126.1:c.970T=	XP_011511428.1:p.Cys324=
XM_011513127.1:c.838T=	XP_011511429.1:p.Cys280=
XM_006713743.4:c.1084T=	XP_006713806.1:p.Cys362=
XM_017007178.2:c.926-19T=	XP_016862667.1:n.926-19T=
NM_024548.4:c.1186T= MANE Select	NP_078824.2:p.Cys396=
NM_001303401.2:c.1028-19T=	NP_001290330.1:n.1028-19T=