Canonical Allele Identifier: CA1388867383

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757715C= , CM000665.2:g.101757715C=	GRCh38
NC_000003.11:g.101476559C= , CM000665.1:g.101476559C=	GRCh37
NC_000003.10:g.102959249C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*744C=	ENSP00000419009.1:n.*744C=
ENST00000467655.2:c.*196C=	ENSP00000418547.2:n.*196C=
ENST00000704365.1:c.1109C=	ENSP00000515873.1:p.Ala370=
ENST00000704366.1:c.1007C=	ENSP00000515874.1:p.Ala336=
ENST00000704367.1:c.926-96C=	ENSP00000515875.1:n.926-96C=
ENST00000704368.1:n.1602C=
ENST00000704369.1:c.623C=	ENSP00000515876.1:p.Ala208=
ENST00000704370.1:c.1103C=	ENSP00000515877.1:p.Ala368=
ENST00000704372.1:n.1463C=
ENST00000704444.1:c.893C=	ENSP00000515896.1:p.Ala298=
ENST00000704445.1:c.761C=	ENSP00000515897.1:p.Ala254=
ENST00000704446.1:c.1048+519C=	ENSP00000515898.1:n.1048+519C=
ENST00000341893.8:c.1109C= MANE Select	ENSP00000342510.3:p.Ala370=
ENST00000341893.7:c.1109C=	ENSP00000342510.3:p.Ala370=
ENST00000467655.1:c.724C=	ENSP00000418547.1:n.724C=
ENST00000489172.5:n.1091C=
ENST00000494050.5:c.1028-96C=	ENSP00000418185.1:n.1028-96C=
NM_001303401.1:c.1028-96C=	NP_001290330.1:n.1028-96C=
NM_024548.3:c.1109C=	NP_078824.2:p.Ala370=
XM_006713743.2:c.1007C=	XP_006713806.1:p.Ala336=
XM_011513125.1:c.893C=	XP_011511427.1:p.Ala298=
XM_011513126.1:c.893C=	XP_011511428.1:p.Ala298=
XM_011513127.1:c.761C=	XP_011511429.1:p.Ala254=
XM_006713743.4:c.1007C=	XP_006713806.1:p.Ala336=
XM_017007178.2:c.926-96C=	XP_016862667.1:n.926-96C=
NM_024548.4:c.1109C= MANE Select	NP_078824.2:p.Ala370=
NM_001303401.2:c.1028-96C=	NP_001290330.1:n.1028-96C=