Canonical Allele Identifier: CA1388867560

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758166T= , CM000665.2:g.101758166T=	GRCh38
NC_000003.11:g.101477010T= , CM000665.1:g.101477010T=	GRCh37
NC_000003.10:g.102959700T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1195T=	ENSP00000419009.1:n.*1195T=
ENST00000467655.2:c.*647T=	ENSP00000418547.2:n.*647T=
ENST00000704365.1:c.1560T=	ENSP00000515873.1:p.Asn520=
ENST00000704366.1:c.1458T=	ENSP00000515874.1:p.Asn486=
ENST00000704367.1:c.1281T=	ENSP00000515875.1:p.Asn427=
ENST00000704368.1:n.2053T=
ENST00000704369.1:c.1074T=	ENSP00000515876.1:p.Asn358=
ENST00000704370.1:c.1554T=	ENSP00000515877.1:p.Asn518=
ENST00000704372.1:n.1914T=
ENST00000704444.1:c.1344T=	ENSP00000515896.1:p.Asn448=
ENST00000704445.1:c.1212T=	ENSP00000515897.1:p.Asn404=
ENST00000704446.1:c.1048+970T=	ENSP00000515898.1:n.1048+970T=
ENST00000341893.8:c.1560T= MANE Select	ENSP00000342510.3:p.Asn520=
ENST00000341893.7:c.1560T=	ENSP00000342510.3:p.Asn520=
ENST00000467655.1:c.1175T=	ENSP00000418547.1:n.1175T=
ENST00000489172.5:n.1542T=
ENST00000494050.5:c.1383T=	ENSP00000418185.1:p.Asn461=
NM_001303401.1:c.1383T=	NP_001290330.1:p.Asn461=
NM_024548.3:c.1560T=	NP_078824.2:p.Asn520=
XM_006713743.2:c.1458T=	XP_006713806.1:p.Asn486=
XM_011513125.1:c.1344T=	XP_011511427.1:p.Asn448=
XM_011513126.1:c.1344T=	XP_011511428.1:p.Asn448=
XM_011513127.1:c.1212T=	XP_011511429.1:p.Asn404=
XM_006713743.4:c.1458T=	XP_006713806.1:p.Asn486=
XM_017007178.2:c.1281T=	XP_016862667.1:p.Asn427=
NM_024548.4:c.1560T= MANE Select	NP_078824.2:p.Asn520=
NM_001303401.2:c.1383T=	NP_001290330.1:p.Asn461=