Canonical Allele Identifier: CA353877675

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476929C>G (hg19) ; chr3:g.101758085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758085C>G , CM000665.2:g.101758085C>G	GRCh38
NC_000003.11:g.101476929C>G , CM000665.1:g.101476929C>G	GRCh37
NC_000003.10:g.102959619C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1114C>G	ENSP00000419009.1:n.*1114C>G
ENST00000467655.2:c.*566C>G	ENSP00000418547.2:n.*566C>G
ENST00000704365.1:c.1479C>G	ENSP00000515873.1:p.Ile493Met
ENST00000704366.1:c.1377C>G	ENSP00000515874.1:p.Ile459Met
ENST00000704367.1:c.1200C>G	ENSP00000515875.1:p.Ile400Met
ENST00000704368.1:n.1972C>G
ENST00000704369.1:c.993C>G	ENSP00000515876.1:p.Ile331Met
ENST00000704370.1:c.1473C>G	ENSP00000515877.1:p.Ile491Met
ENST00000704372.1:n.1833C>G
ENST00000704444.1:c.1263C>G	ENSP00000515896.1:p.Ile421Met
ENST00000704445.1:c.1131C>G	ENSP00000515897.1:p.Ile377Met
ENST00000704446.1:c.1048+889C>G	ENSP00000515898.1:n.1048+889C>G
ENST00000341893.8:c.1479C>G MANE Select	ENSP00000342510.3:p.Ile493Met
ENST00000341893.7:c.1479C>G	ENSP00000342510.3:p.Ile493Met
ENST00000467655.1:c.1094C>G	ENSP00000418547.1:n.1094C>G
ENST00000489172.5:n.1461C>G
ENST00000494050.5:c.1302C>G	ENSP00000418185.1:p.Ile434Met
NM_001303401.1:c.1302C>G	NP_001290330.1:p.Ile434Met
NM_024548.3:c.1479C>G	NP_078824.2:p.Ile493Met
XM_006713743.2:c.1377C>G	XP_006713806.1:p.Ile459Met
XM_011513125.1:c.1263C>G	XP_011511427.1:p.Ile421Met
XM_011513126.1:c.1263C>G	XP_011511428.1:p.Ile421Met
XM_011513127.1:c.1131C>G	XP_011511429.1:p.Ile377Met
XM_006713743.4:c.1377C>G	XP_006713806.1:p.Ile459Met
XM_017007178.2:c.1200C>G	XP_016862667.1:p.Ile400Met
NM_024548.4:c.1479C>G MANE Select	NP_078824.2:p.Ile493Met
NM_001303401.2:c.1302C>G	NP_001290330.1:p.Ile434Met