Canonical Allele Identifier: CA353877715

Gene: CEP97

Linked Data

• gnomAD v4: 3-101758101-C-T
• MyVariant Identifiers: chr3:g.101476945C>T (hg19) ; chr3:g.101758101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758101C>T , CM000665.2:g.101758101C>T	GRCh38
NC_000003.11:g.101476945C>T , CM000665.1:g.101476945C>T	GRCh37
NC_000003.10:g.102959635C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1130C>T	ENSP00000419009.1:n.*1130C>T
ENST00000467655.2:c.*582C>T	ENSP00000418547.2:n.*582C>T
ENST00000704365.1:c.1495C>T	ENSP00000515873.1:p.His499Tyr
ENST00000704366.1:c.1393C>T	ENSP00000515874.1:p.His465Tyr
ENST00000704367.1:c.1216C>T	ENSP00000515875.1:p.His406Tyr
ENST00000704368.1:n.1988C>T
ENST00000704369.1:c.1009C>T	ENSP00000515876.1:p.His337Tyr
ENST00000704370.1:c.1489C>T	ENSP00000515877.1:p.His497Tyr
ENST00000704372.1:n.1849C>T
ENST00000704444.1:c.1279C>T	ENSP00000515896.1:p.His427Tyr
ENST00000704445.1:c.1147C>T	ENSP00000515897.1:p.His383Tyr
ENST00000704446.1:c.1048+905C>T	ENSP00000515898.1:n.1048+905C>T
ENST00000341893.8:c.1495C>T MANE Select	ENSP00000342510.3:p.His499Tyr
ENST00000341893.7:c.1495C>T	ENSP00000342510.3:p.His499Tyr
ENST00000467655.1:c.1110C>T	ENSP00000418547.1:n.1110C>T
ENST00000489172.5:n.1477C>T
ENST00000494050.5:c.1318C>T	ENSP00000418185.1:p.His440Tyr
NM_001303401.1:c.1318C>T	NP_001290330.1:p.His440Tyr
NM_024548.3:c.1495C>T	NP_078824.2:p.His499Tyr
XM_006713743.2:c.1393C>T	XP_006713806.1:p.His465Tyr
XM_011513125.1:c.1279C>T	XP_011511427.1:p.His427Tyr
XM_011513126.1:c.1279C>T	XP_011511428.1:p.His427Tyr
XM_011513127.1:c.1147C>T	XP_011511429.1:p.His383Tyr
XM_006713743.4:c.1393C>T	XP_006713806.1:p.His465Tyr
XM_017007178.2:c.1216C>T	XP_016862667.1:p.His406Tyr
NM_024548.4:c.1495C>T MANE Select	NP_078824.2:p.His499Tyr
NM_001303401.2:c.1318C>T	NP_001290330.1:p.His440Tyr