Canonical Allele Identifier: CA1388867335

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757582_101757583delinsAC , CM000665.2:g.101757582_101757583delinsAC	GRCh38
NC_000003.11:g.101476426_101476427delinsAC , CM000665.1:g.101476426_101476427delinsAC	GRCh37
NC_000003.10:g.102959116_102959117delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*663-52_*663-51delinsAC	ENSP00000419009.1:n.*663-52_*663-51delinsAC
ENST00000467655.2:c.*115-52_*115-51delinsAC	ENSP00000418547.2:n.*115-52_*115-51delinsAC
ENST00000704365.1:c.1028-52_1028-51delinsAC	ENSP00000515873.1:n.1028-52_1028-51delinsAC
ENST00000704366.1:c.926-52_926-51delinsAC	ENSP00000515874.1:n.926-52_926-51delinsAC
ENST00000704367.1:c.926-229_926-228delinsAC	ENSP00000515875.1:n.926-229_926-228delinsAC
ENST00000704368.1:n.1469_1470delinsAC
ENST00000704369.1:c.542-52_542-51delinsAC	ENSP00000515876.1:n.542-52_542-51delinsAC
ENST00000704370.1:c.1022-52_1022-51delinsAC	ENSP00000515877.1:n.1022-52_1022-51delinsAC
ENST00000704372.1:n.1382-52_1382-51delinsAC
ENST00000704444.1:c.812-52_812-51delinsAC	ENSP00000515896.1:n.812-52_812-51delinsAC
ENST00000704445.1:c.680-52_680-51delinsAC	ENSP00000515897.1:n.680-52_680-51delinsAC
ENST00000704446.1:c.1048+386_1048+387delinsAC	ENSP00000515898.1:n.1048+386_1048+387delinsAC
ENST00000341893.8:c.1028-52_1028-51delinsAC MANE Select	ENSP00000342510.3:n.1028-52_1028-51delinsAC
ENST00000341893.7:c.1028-52_1028-51delinsAC	ENSP00000342510.3:n.1028-52_1028-51delinsAC
ENST00000467655.1:c.643-52_643-51delinsAC	ENSP00000418547.1:n.643-52_643-51delinsAC
ENST00000489172.5:n.1010-52_1010-51delinsAC
ENST00000494050.5:c.1028-229_1028-228delinsAC	ENSP00000418185.1:n.1028-229_1028-228delinsAC
NM_001303401.1:c.1028-229_1028-228delinsAC	NP_001290330.1:n.1028-229_1028-228delinsAC
NM_024548.3:c.1028-52_1028-51delinsAC	NP_078824.2:n.1028-52_1028-51delinsAC
XM_006713743.2:c.926-52_926-51delinsAC	XP_006713806.1:n.926-52_926-51delinsAC
XM_011513125.1:c.812-52_812-51delinsAC	XP_011511427.1:n.812-52_812-51delinsAC
XM_011513126.1:c.812-52_812-51delinsAC	XP_011511428.1:n.812-52_812-51delinsAC
XM_011513127.1:c.680-52_680-51delinsAC	XP_011511429.1:n.680-52_680-51delinsAC
XM_006713743.4:c.926-52_926-51delinsAC	XP_006713806.1:n.926-52_926-51delinsAC
XM_017007178.2:c.926-229_926-228delinsAC	XP_016862667.1:n.926-229_926-228delinsAC
NM_024548.4:c.1028-52_1028-51delinsAC MANE Select	NP_078824.2:n.1028-52_1028-51delinsAC
NM_001303401.2:c.1028-229_1028-228delinsAC	NP_001290330.1:n.1028-229_1028-228delinsAC