Canonical Allele Identifier: CA1388867301

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757496G= , CM000665.2:g.101757496G=	GRCh38
NC_000003.11:g.101476340G= , CM000665.1:g.101476340G=	GRCh37
NC_000003.10:g.102959030G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*663-138G=	ENSP00000419009.1:n.*663-138G=
ENST00000467655.2:c.*115-138G=	ENSP00000418547.2:n.*115-138G=
ENST00000704365.1:c.1028-138G=	ENSP00000515873.1:n.1028-138G=
ENST00000704366.1:c.926-138G=	ENSP00000515874.1:n.926-138G=
ENST00000704367.1:c.925+300G=	ENSP00000515875.1:n.925+300G=
ENST00000704368.1:n.1383G=
ENST00000704369.1:c.542-138G=	ENSP00000515876.1:n.542-138G=
ENST00000704370.1:c.1022-138G=	ENSP00000515877.1:n.1022-138G=
ENST00000704372.1:n.1382-138G=
ENST00000704444.1:c.812-138G=	ENSP00000515896.1:n.812-138G=
ENST00000704445.1:c.680-138G=	ENSP00000515897.1:n.680-138G=
ENST00000704446.1:c.1048+300G=	ENSP00000515898.1:n.1048+300G=
ENST00000341893.8:c.1028-138G= MANE Select	ENSP00000342510.3:n.1028-138G=
ENST00000341893.7:c.1028-138G=	ENSP00000342510.3:n.1028-138G=
ENST00000467655.1:c.643-138G=	ENSP00000418547.1:n.643-138G=
ENST00000489172.5:n.1010-138G=
ENST00000494050.5:c.1027+300G=	ENSP00000418185.1:n.1027+300G=
NM_001303401.1:c.1027+300G=	NP_001290330.1:n.1027+300G=
NM_024548.3:c.1028-138G=	NP_078824.2:n.1028-138G=
XM_006713743.2:c.926-138G=	XP_006713806.1:n.926-138G=
XM_011513125.1:c.812-138G=	XP_011511427.1:n.812-138G=
XM_011513126.1:c.812-138G=	XP_011511428.1:n.812-138G=
XM_011513127.1:c.680-138G=	XP_011511429.1:n.680-138G=
XM_006713743.4:c.926-138G=	XP_006713806.1:n.926-138G=
XM_017007178.2:c.925+300G=	XP_016862667.1:n.925+300G=
NM_024548.4:c.1028-138G= MANE Select	NP_078824.2:n.1028-138G=
NM_001303401.2:c.1027+300G=	NP_001290330.1:n.1027+300G=