Canonical Allele Identifier: CA1388867541

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758112A= , CM000665.2:g.101758112A=	GRCh38
NC_000003.11:g.101476956A= , CM000665.1:g.101476956A=	GRCh37
NC_000003.10:g.102959646A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1141A=	ENSP00000419009.1:n.*1141A=
ENST00000467655.2:c.*593A=	ENSP00000418547.2:n.*593A=
ENST00000704365.1:c.1506A=	ENSP00000515873.1:p.Thr502=
ENST00000704366.1:c.1404A=	ENSP00000515874.1:p.Thr468=
ENST00000704367.1:c.1227A=	ENSP00000515875.1:p.Thr409=
ENST00000704368.1:n.1999A=
ENST00000704369.1:c.1020A=	ENSP00000515876.1:p.Thr340=
ENST00000704370.1:c.1500A=	ENSP00000515877.1:p.Thr500=
ENST00000704372.1:n.1860A=
ENST00000704444.1:c.1290A=	ENSP00000515896.1:p.Thr430=
ENST00000704445.1:c.1158A=	ENSP00000515897.1:p.Thr386=
ENST00000704446.1:c.1048+916A=	ENSP00000515898.1:n.1048+916A=
ENST00000341893.8:c.1506A= MANE Select	ENSP00000342510.3:p.Thr502=
ENST00000341893.7:c.1506A=	ENSP00000342510.3:p.Thr502=
ENST00000467655.1:c.1121A=	ENSP00000418547.1:n.1121A=
ENST00000489172.5:n.1488A=
ENST00000494050.5:c.1329A=	ENSP00000418185.1:p.Thr443=
NM_001303401.1:c.1329A=	NP_001290330.1:p.Thr443=
NM_024548.3:c.1506A=	NP_078824.2:p.Thr502=
XM_006713743.2:c.1404A=	XP_006713806.1:p.Thr468=
XM_011513125.1:c.1290A=	XP_011511427.1:p.Thr430=
XM_011513126.1:c.1290A=	XP_011511428.1:p.Thr430=
XM_011513127.1:c.1158A=	XP_011511429.1:p.Thr386=
XM_006713743.4:c.1404A=	XP_006713806.1:p.Thr468=
XM_017007178.2:c.1227A=	XP_016862667.1:p.Thr409=
NM_024548.4:c.1506A= MANE Select	NP_078824.2:p.Thr502=
NM_001303401.2:c.1329A=	NP_001290330.1:p.Thr443=