Canonical Allele Identifier: CA2522140

Gene: CEP97

Linked Data

• ClinVar Variation Id: 2165320
• ClinVar RCV Id: RCV003089917
• dbSNP Id: rs761985984
• ExAC: 3:101476952 T / C
• gnomAD v2: 3-101476952-T-C
• gnomAD v3: 3-101758108-T-C
• gnomAD v4: 3-101758108-T-C
• MyVariant Identifiers: chr3:g.101476952T>C (hg19) ; chr3:g.101758108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758108T>C , CM000665.2:g.101758108T>C	GRCh38
NC_000003.11:g.101476952T>C , CM000665.1:g.101476952T>C	GRCh37
NC_000003.10:g.102959642T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1137T>C	ENSP00000419009.1:n.*1137T>C
ENST00000467655.2:c.*589T>C	ENSP00000418547.2:n.*589T>C
ENST00000704365.1:c.1502T>C	ENSP00000515873.1:p.Leu501Pro
ENST00000704366.1:c.1400T>C	ENSP00000515874.1:p.Leu467Pro
ENST00000704367.1:c.1223T>C	ENSP00000515875.1:p.Leu408Pro
ENST00000704368.1:n.1995T>C
ENST00000704369.1:c.1016T>C	ENSP00000515876.1:p.Leu339Pro
ENST00000704370.1:c.1496T>C	ENSP00000515877.1:p.Leu499Pro
ENST00000704372.1:n.1856T>C
ENST00000704444.1:c.1286T>C	ENSP00000515896.1:p.Leu429Pro
ENST00000704445.1:c.1154T>C	ENSP00000515897.1:p.Leu385Pro
ENST00000704446.1:c.1048+912T>C	ENSP00000515898.1:n.1048+912T>C
ENST00000341893.8:c.1502T>C MANE Select	ENSP00000342510.3:p.Leu501Pro
ENST00000341893.7:c.1502T>C	ENSP00000342510.3:p.Leu501Pro
ENST00000467655.1:c.1117T>C	ENSP00000418547.1:n.1117T>C
ENST00000489172.5:n.1484T>C
ENST00000494050.5:c.1325T>C	ENSP00000418185.1:p.Leu442Pro
NM_001303401.1:c.1325T>C	NP_001290330.1:p.Leu442Pro
NM_024548.3:c.1502T>C	NP_078824.2:p.Leu501Pro
XM_006713743.2:c.1400T>C	XP_006713806.1:p.Leu467Pro
XM_011513125.1:c.1286T>C	XP_011511427.1:p.Leu429Pro
XM_011513126.1:c.1286T>C	XP_011511428.1:p.Leu429Pro
XM_011513127.1:c.1154T>C	XP_011511429.1:p.Leu385Pro
XM_006713743.4:c.1400T>C	XP_006713806.1:p.Leu467Pro
XM_017007178.2:c.1223T>C	XP_016862667.1:p.Leu408Pro
NM_024548.4:c.1502T>C MANE Select	NP_078824.2:p.Leu501Pro
NM_001303401.2:c.1325T>C	NP_001290330.1:p.Leu442Pro