Canonical Allele Identifier: CA1388867552

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758148C= , CM000665.2:g.101758148C=	GRCh38
NC_000003.11:g.101476992C= , CM000665.1:g.101476992C=	GRCh37
NC_000003.10:g.102959682C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1177C=	ENSP00000419009.1:n.*1177C=
ENST00000467655.2:c.*629C=	ENSP00000418547.2:n.*629C=
ENST00000704365.1:c.1542C=	ENSP00000515873.1:p.Asp514=
ENST00000704366.1:c.1440C=	ENSP00000515874.1:p.Asp480=
ENST00000704367.1:c.1263C=	ENSP00000515875.1:p.Asp421=
ENST00000704368.1:n.2035C=
ENST00000704369.1:c.1056C=	ENSP00000515876.1:p.Asp352=
ENST00000704370.1:c.1536C=	ENSP00000515877.1:p.Asp512=
ENST00000704372.1:n.1896C=
ENST00000704444.1:c.1326C=	ENSP00000515896.1:p.Asp442=
ENST00000704445.1:c.1194C=	ENSP00000515897.1:p.Asp398=
ENST00000704446.1:c.1048+952C=	ENSP00000515898.1:n.1048+952C=
ENST00000341893.8:c.1542C= MANE Select	ENSP00000342510.3:p.Asp514=
ENST00000341893.7:c.1542C=	ENSP00000342510.3:p.Asp514=
ENST00000467655.1:c.1157C=	ENSP00000418547.1:n.1157C=
ENST00000489172.5:n.1524C=
ENST00000494050.5:c.1365C=	ENSP00000418185.1:p.Asp455=
NM_001303401.1:c.1365C=	NP_001290330.1:p.Asp455=
NM_024548.3:c.1542C=	NP_078824.2:p.Asp514=
XM_006713743.2:c.1440C=	XP_006713806.1:p.Asp480=
XM_011513125.1:c.1326C=	XP_011511427.1:p.Asp442=
XM_011513126.1:c.1326C=	XP_011511428.1:p.Asp442=
XM_011513127.1:c.1194C=	XP_011511429.1:p.Asp398=
XM_006713743.4:c.1440C=	XP_006713806.1:p.Asp480=
XM_017007178.2:c.1263C=	XP_016862667.1:p.Asp421=
NM_024548.4:c.1542C= MANE Select	NP_078824.2:p.Asp514=
NM_001303401.2:c.1365C=	NP_001290330.1:p.Asp455=