Canonical Allele Identifier: CA1388867311

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757528_101757529delinsGA , CM000665.2:g.101757528_101757529delinsGA	GRCh38
NC_000003.11:g.101476372_101476373delinsGA , CM000665.1:g.101476372_101476373delinsGA	GRCh37
NC_000003.10:g.102959062_102959063delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*663-106_*663-105delinsGA	ENSP00000419009.1:n.*663-106_*663-105delinsGA
ENST00000467655.2:c.*115-106_*115-105delinsGA	ENSP00000418547.2:n.*115-106_*115-105delinsGA
ENST00000704365.1:c.1028-106_1028-105delinsGA	ENSP00000515873.1:n.1028-106_1028-105delinsGA
ENST00000704366.1:c.926-106_926-105delinsGA	ENSP00000515874.1:n.926-106_926-105delinsGA
ENST00000704367.1:c.926-283_926-282delinsGA	ENSP00000515875.1:n.926-283_926-282delinsGA
ENST00000704368.1:n.1415_1416delinsGA
ENST00000704369.1:c.542-106_542-105delinsGA	ENSP00000515876.1:n.542-106_542-105delinsGA
ENST00000704370.1:c.1022-106_1022-105delinsGA	ENSP00000515877.1:n.1022-106_1022-105delinsGA
ENST00000704372.1:n.1382-106_1382-105delinsGA
ENST00000704444.1:c.812-106_812-105delinsGA	ENSP00000515896.1:n.812-106_812-105delinsGA
ENST00000704445.1:c.680-106_680-105delinsGA	ENSP00000515897.1:n.680-106_680-105delinsGA
ENST00000704446.1:c.1048+332_1048+333delinsGA	ENSP00000515898.1:n.1048+332_1048+333delinsGA
ENST00000341893.8:c.1028-106_1028-105delinsGA MANE Select	ENSP00000342510.3:n.1028-106_1028-105delinsGA
ENST00000341893.7:c.1028-106_1028-105delinsGA	ENSP00000342510.3:n.1028-106_1028-105delinsGA
ENST00000467655.1:c.643-106_643-105delinsGA	ENSP00000418547.1:n.643-106_643-105delinsGA
ENST00000489172.5:n.1010-106_1010-105delinsGA
ENST00000494050.5:c.1028-283_1028-282delinsGA	ENSP00000418185.1:n.1028-283_1028-282delinsGA
NM_001303401.1:c.1028-283_1028-282delinsGA	NP_001290330.1:n.1028-283_1028-282delinsGA
NM_024548.3:c.1028-106_1028-105delinsGA	NP_078824.2:n.1028-106_1028-105delinsGA
XM_006713743.2:c.926-106_926-105delinsGA	XP_006713806.1:n.926-106_926-105delinsGA
XM_011513125.1:c.812-106_812-105delinsGA	XP_011511427.1:n.812-106_812-105delinsGA
XM_011513126.1:c.812-106_812-105delinsGA	XP_011511428.1:n.812-106_812-105delinsGA
XM_011513127.1:c.680-106_680-105delinsGA	XP_011511429.1:n.680-106_680-105delinsGA
XM_006713743.4:c.926-106_926-105delinsGA	XP_006713806.1:n.926-106_926-105delinsGA
XM_017007178.2:c.926-283_926-282delinsGA	XP_016862667.1:n.926-283_926-282delinsGA
NM_024548.4:c.1028-106_1028-105delinsGA MANE Select	NP_078824.2:n.1028-106_1028-105delinsGA
NM_001303401.2:c.1028-283_1028-282delinsGA	NP_001290330.1:n.1028-283_1028-282delinsGA