Canonical Allele Identifier: CA1388867502

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758009G= , CM000665.2:g.101758009G=	GRCh38
NC_000003.11:g.101476853G= , CM000665.1:g.101476853G=	GRCh37
NC_000003.10:g.102959543G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1038G=	ENSP00000419009.1:n.*1038G=
ENST00000467655.2:c.*490G=	ENSP00000418547.2:n.*490G=
ENST00000704365.1:c.1403G=	ENSP00000515873.1:p.Arg468=
ENST00000704366.1:c.1301G=	ENSP00000515874.1:p.Arg434=
ENST00000704367.1:c.1124G=	ENSP00000515875.1:p.Arg375=
ENST00000704368.1:n.1896G=
ENST00000704369.1:c.917G=	ENSP00000515876.1:p.Arg306=
ENST00000704370.1:c.1397G=	ENSP00000515877.1:p.Arg466=
ENST00000704372.1:n.1757G=
ENST00000704444.1:c.1187G=	ENSP00000515896.1:p.Arg396=
ENST00000704445.1:c.1055G=	ENSP00000515897.1:p.Arg352=
ENST00000704446.1:c.1048+813G=	ENSP00000515898.1:n.1048+813G=
ENST00000341893.8:c.1403G= MANE Select	ENSP00000342510.3:p.Arg468=
ENST00000341893.7:c.1403G=	ENSP00000342510.3:p.Arg468=
ENST00000467655.1:c.1018G=	ENSP00000418547.1:n.1018G=
ENST00000489172.5:n.1385G=
ENST00000494050.5:c.1226G=	ENSP00000418185.1:p.Arg409=
NM_001303401.1:c.1226G=	NP_001290330.1:p.Arg409=
NM_024548.3:c.1403G=	NP_078824.2:p.Arg468=
XM_006713743.2:c.1301G=	XP_006713806.1:p.Arg434=
XM_011513125.1:c.1187G=	XP_011511427.1:p.Arg396=
XM_011513126.1:c.1187G=	XP_011511428.1:p.Arg396=
XM_011513127.1:c.1055G=	XP_011511429.1:p.Arg352=
XM_006713743.4:c.1301G=	XP_006713806.1:p.Arg434=
XM_017007178.2:c.1124G=	XP_016862667.1:p.Arg375=
NM_024548.4:c.1403G= MANE Select	NP_078824.2:p.Arg468=
NM_001303401.2:c.1226G=	NP_001290330.1:p.Arg409=