Canonical Allele Identifier: CA353877593

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476889G>T (hg19) ; chr3:g.101758045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758045G>T , CM000665.2:g.101758045G>T	GRCh38
NC_000003.11:g.101476889G>T , CM000665.1:g.101476889G>T	GRCh37
NC_000003.10:g.102959579G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1074G>T	ENSP00000419009.1:n.*1074G>T
ENST00000467655.2:c.*526G>T	ENSP00000418547.2:n.*526G>T
ENST00000704365.1:c.1439G>T	ENSP00000515873.1:p.Gly480Val
ENST00000704366.1:c.1337G>T	ENSP00000515874.1:p.Gly446Val
ENST00000704367.1:c.1160G>T	ENSP00000515875.1:p.Gly387Val
ENST00000704368.1:n.1932G>T
ENST00000704369.1:c.953G>T	ENSP00000515876.1:p.Gly318Val
ENST00000704370.1:c.1433G>T	ENSP00000515877.1:p.Gly478Val
ENST00000704372.1:n.1793G>T
ENST00000704444.1:c.1223G>T	ENSP00000515896.1:p.Gly408Val
ENST00000704445.1:c.1091G>T	ENSP00000515897.1:p.Gly364Val
ENST00000704446.1:c.1048+849G>T	ENSP00000515898.1:n.1048+849G>T
ENST00000341893.8:c.1439G>T MANE Select	ENSP00000342510.3:p.Gly480Val
ENST00000341893.7:c.1439G>T	ENSP00000342510.3:p.Gly480Val
ENST00000467655.1:c.1054G>T	ENSP00000418547.1:n.1054G>T
ENST00000489172.5:n.1421G>T
ENST00000494050.5:c.1262G>T	ENSP00000418185.1:p.Gly421Val
NM_001303401.1:c.1262G>T	NP_001290330.1:p.Gly421Val
NM_024548.3:c.1439G>T	NP_078824.2:p.Gly480Val
XM_006713743.2:c.1337G>T	XP_006713806.1:p.Gly446Val
XM_011513125.1:c.1223G>T	XP_011511427.1:p.Gly408Val
XM_011513126.1:c.1223G>T	XP_011511428.1:p.Gly408Val
XM_011513127.1:c.1091G>T	XP_011511429.1:p.Gly364Val
XM_006713743.4:c.1337G>T	XP_006713806.1:p.Gly446Val
XM_017007178.2:c.1160G>T	XP_016862667.1:p.Gly387Val
NM_024548.4:c.1439G>T MANE Select	NP_078824.2:p.Gly480Val
NM_001303401.2:c.1262G>T	NP_001290330.1:p.Gly421Val