Canonical Allele Identifier: CA79768602

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476553_101476554insC (hg19) ; chr3:g.101757709_101757710insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757709_101757710insC , CM000665.2:g.101757709_101757710insC	GRCh38
NC_000003.11:g.101476553_101476554insC , CM000665.1:g.101476553_101476554insC	GRCh37
NC_000003.10:g.102959243_102959244insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*738_*739insC	ENSP00000419009.1:n.*738_*739insC
ENST00000467655.2:c.*190_*191insC	ENSP00000418547.2:n.*190_*191insC
ENST00000704365.1:c.1103_1104insC	ENSP00000515873.1:p.Pro369SerfsTer13
ENST00000704366.1:c.1001_1002insC	ENSP00000515874.1:p.Pro335SerfsTer13
ENST00000704367.1:c.926-102_926-101insC	ENSP00000515875.1:n.926-102_926-101insC
ENST00000704368.1:n.1596_1597insC
ENST00000704369.1:c.617_618insC	ENSP00000515876.1:p.Pro207SerfsTer13
ENST00000704370.1:c.1097_1098insC	ENSP00000515877.1:p.Pro367SerfsTer13
ENST00000704372.1:n.1457_1458insC
ENST00000704444.1:c.887_888insC	ENSP00000515896.1:p.Pro297SerfsTer13
ENST00000704445.1:c.755_756insC	ENSP00000515897.1:p.Pro253SerfsTer13
ENST00000704446.1:c.1048+513_1048+514insC	ENSP00000515898.1:n.1048+513_1048+514insC
ENST00000341893.8:c.1103_1104insC MANE Select	ENSP00000342510.3:p.Pro369SerfsTer13
ENST00000341893.7:c.1103_1104insC	ENSP00000342510.3:p.Pro369SerfsTer13
ENST00000467655.1:c.718_719insC	ENSP00000418547.1:n.718_719insC
ENST00000489172.5:n.1085_1086insC
ENST00000494050.5:c.1028-102_1028-101insC	ENSP00000418185.1:n.1028-102_1028-101insC
NM_001303401.1:c.1028-102_1028-101insC	NP_001290330.1:n.1028-102_1028-101insC
NM_024548.3:c.1103_1104insC	NP_078824.2:p.Pro369SerfsTer13
XM_006713743.2:c.1001_1002insC	XP_006713806.1:p.Pro335SerfsTer13
XM_011513125.1:c.887_888insC	XP_011511427.1:p.Pro297SerfsTer13
XM_011513126.1:c.887_888insC	XP_011511428.1:p.Pro297SerfsTer13
XM_011513127.1:c.755_756insC	XP_011511429.1:p.Pro253SerfsTer13
XM_006713743.4:c.1001_1002insC	XP_006713806.1:p.Pro335SerfsTer13
XM_017007178.2:c.926-102_926-101insC	XP_016862667.1:n.926-102_926-101insC
NM_024548.4:c.1103_1104insC MANE Select	NP_078824.2:p.Pro369SerfsTer13
NM_001303401.2:c.1028-102_1028-101insC	NP_001290330.1:n.1028-102_1028-101insC