Canonical Allele Identifier: CA1388867447

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757849C= , CM000665.2:g.101757849C=	GRCh38
NC_000003.11:g.101476693C= , CM000665.1:g.101476693C=	GRCh37
NC_000003.10:g.102959383C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*878C=	ENSP00000419009.1:n.*878C=
ENST00000467655.2:c.*330C=	ENSP00000418547.2:n.*330C=
ENST00000704365.1:c.1243C=	ENSP00000515873.1:p.Leu415=
ENST00000704366.1:c.1141C=	ENSP00000515874.1:p.Leu381=
ENST00000704367.1:c.964C=	ENSP00000515875.1:p.Leu322=
ENST00000704368.1:n.1736C=
ENST00000704369.1:c.757C=	ENSP00000515876.1:p.Leu253=
ENST00000704370.1:c.1237C=	ENSP00000515877.1:p.Leu413=
ENST00000704372.1:n.1597C=
ENST00000704444.1:c.1027C=	ENSP00000515896.1:p.Leu343=
ENST00000704445.1:c.895C=	ENSP00000515897.1:p.Leu299=
ENST00000704446.1:c.1048+653C=	ENSP00000515898.1:n.1048+653C=
ENST00000341893.8:c.1243C= MANE Select	ENSP00000342510.3:p.Leu415=
ENST00000341893.7:c.1243C=	ENSP00000342510.3:p.Leu415=
ENST00000467655.1:c.858C=	ENSP00000418547.1:n.858C=
ENST00000489172.5:n.1225C=
ENST00000494050.5:c.1066C=	ENSP00000418185.1:p.Leu356=
NM_001303401.1:c.1066C=	NP_001290330.1:p.Leu356=
NM_024548.3:c.1243C=	NP_078824.2:p.Leu415=
XM_006713743.2:c.1141C=	XP_006713806.1:p.Leu381=
XM_011513125.1:c.1027C=	XP_011511427.1:p.Leu343=
XM_011513126.1:c.1027C=	XP_011511428.1:p.Leu343=
XM_011513127.1:c.895C=	XP_011511429.1:p.Leu299=
XM_006713743.4:c.1141C=	XP_006713806.1:p.Leu381=
XM_017007178.2:c.964C=	XP_016862667.1:p.Leu322=
NM_024548.4:c.1243C= MANE Select	NP_078824.2:p.Leu415=
NM_001303401.2:c.1066C=	NP_001290330.1:p.Leu356=