Canonical Allele Identifier: CA353877616

Gene: CEP97

Linked Data

• gnomAD v4: 3-101758057-G-C
• MyVariant Identifiers: chr3:g.101476901G>C (hg19) ; chr3:g.101758057G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758057G>C , CM000665.2:g.101758057G>C	GRCh38
NC_000003.11:g.101476901G>C , CM000665.1:g.101476901G>C	GRCh37
NC_000003.10:g.102959591G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1086G>C	ENSP00000419009.1:n.*1086G>C
ENST00000467655.2:c.*538G>C	ENSP00000418547.2:n.*538G>C
ENST00000704365.1:c.1451G>C	ENSP00000515873.1:p.Cys484Ser
ENST00000704366.1:c.1349G>C	ENSP00000515874.1:p.Cys450Ser
ENST00000704367.1:c.1172G>C	ENSP00000515875.1:p.Cys391Ser
ENST00000704368.1:n.1944G>C
ENST00000704369.1:c.965G>C	ENSP00000515876.1:p.Cys322Ser
ENST00000704370.1:c.1445G>C	ENSP00000515877.1:p.Cys482Ser
ENST00000704372.1:n.1805G>C
ENST00000704444.1:c.1235G>C	ENSP00000515896.1:p.Cys412Ser
ENST00000704445.1:c.1103G>C	ENSP00000515897.1:p.Cys368Ser
ENST00000704446.1:c.1048+861G>C	ENSP00000515898.1:n.1048+861G>C
ENST00000341893.8:c.1451G>C MANE Select	ENSP00000342510.3:p.Cys484Ser
ENST00000341893.7:c.1451G>C	ENSP00000342510.3:p.Cys484Ser
ENST00000467655.1:c.1066G>C	ENSP00000418547.1:n.1066G>C
ENST00000489172.5:n.1433G>C
ENST00000494050.5:c.1274G>C	ENSP00000418185.1:p.Cys425Ser
NM_001303401.1:c.1274G>C	NP_001290330.1:p.Cys425Ser
NM_024548.3:c.1451G>C	NP_078824.2:p.Cys484Ser
XM_006713743.2:c.1349G>C	XP_006713806.1:p.Cys450Ser
XM_011513125.1:c.1235G>C	XP_011511427.1:p.Cys412Ser
XM_011513126.1:c.1235G>C	XP_011511428.1:p.Cys412Ser
XM_011513127.1:c.1103G>C	XP_011511429.1:p.Cys368Ser
XM_006713743.4:c.1349G>C	XP_006713806.1:p.Cys450Ser
XM_017007178.2:c.1172G>C	XP_016862667.1:p.Cys391Ser
NM_024548.4:c.1451G>C MANE Select	NP_078824.2:p.Cys484Ser
NM_001303401.2:c.1274G>C	NP_001290330.1:p.Cys425Ser