Canonical Allele Identifier: CA434727680

Gene: CEP97

Linked Data

• gnomAD v4: 3-101757665-G-A
• MyVariant Identifiers: chr3:g.101476509G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757665G>A , CM000665.2:g.101757665G>A	GRCh38
NC_000003.11:g.101476509G>A , CM000665.1:g.101476509G>A	GRCh37
NC_000003.10:g.102959199G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000465011.2:c.*694G>A	ENSP00000419009.1:n.*694G>A
ENST00000467655.2:c.*146G>A	ENSP00000418547.2:n.*146G>A
ENST00000704365.1:c.1059G>A	ENSP00000515873.1:p.Gly353=
ENST00000704366.1:c.957G>A	ENSP00000515874.1:p.Gly319=
ENST00000704367.1:c.926-146G>A	ENSP00000515875.1:n.926-146G>A
ENST00000704368.1:n.1552G>A
ENST00000704369.1:c.573G>A	ENSP00000515876.1:p.Gly191=
ENST00000704370.1:c.1053G>A	ENSP00000515877.1:p.Gly351=
ENST00000704372.1:n.1413G>A
ENST00000704444.1:c.843G>A	ENSP00000515896.1:p.Gly281=
ENST00000704445.1:c.711G>A	ENSP00000515897.1:p.Gly237=
ENST00000704446.1:c.1048+469G>A	ENSP00000515898.1:n.1048+469G>A
ENST00000341893.8:c.1059G>A MANE Select	ENSP00000342510.3:p.Gly353=
ENST00000341893.7:c.1059G>A	ENSP00000342510.3:p.Gly353=
ENST00000467655.1:c.674G>A	ENSP00000418547.1:n.674G>A
ENST00000489172.5:n.1041G>A
ENST00000494050.5:c.1028-146G>A	ENSP00000418185.1:n.1028-146G>A
NM_001303401.1:c.1028-146G>A	NP_001290330.1:n.1028-146G>A
NM_024548.3:c.1059G>A	NP_078824.2:p.Gly353=
XM_006713743.2:c.957G>A	XP_006713806.1:p.Gly319=
XM_011513125.1:c.843G>A	XP_011511427.1:p.Gly281=
XM_011513126.1:c.843G>A	XP_011511428.1:p.Gly281=
XM_011513127.1:c.711G>A	XP_011511429.1:p.Gly237=
XM_006713743.4:c.957G>A	XP_006713806.1:p.Gly319=
XM_017007178.2:c.926-146G>A	XP_016862667.1:n.926-146G>A
NM_024548.4:c.1059G>A MANE Select	NP_078824.2:p.Gly353=
NM_001303401.2:c.1028-146G>A	NP_001290330.1:n.1028-146G>A