Canonical Allele Identifier: CA353876212

Gene: CEP97

Linked Data

• gnomAD v4: 3-101757703-A-C
• MyVariant Identifiers: chr3:g.101476547A>C (hg19) ; chr3:g.101757703A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757703A>C , CM000665.2:g.101757703A>C	GRCh38
NC_000003.11:g.101476547A>C , CM000665.1:g.101476547A>C	GRCh37
NC_000003.10:g.102959237A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*732A>C	ENSP00000419009.1:n.*732A>C
ENST00000467655.2:c.*184A>C	ENSP00000418547.2:n.*184A>C
ENST00000704365.1:c.1097A>C	ENSP00000515873.1:p.Asn366Thr
ENST00000704366.1:c.995A>C	ENSP00000515874.1:p.Asn332Thr
ENST00000704367.1:c.926-108A>C	ENSP00000515875.1:n.926-108A>C
ENST00000704368.1:n.1590A>C
ENST00000704369.1:c.611A>C	ENSP00000515876.1:p.Asn204Thr
ENST00000704370.1:c.1091A>C	ENSP00000515877.1:p.Asn364Thr
ENST00000704372.1:n.1451A>C
ENST00000704444.1:c.881A>C	ENSP00000515896.1:p.Asn294Thr
ENST00000704445.1:c.749A>C	ENSP00000515897.1:p.Asn250Thr
ENST00000704446.1:c.1048+507A>C	ENSP00000515898.1:n.1048+507A>C
ENST00000341893.8:c.1097A>C MANE Select	ENSP00000342510.3:p.Asn366Thr
ENST00000341893.7:c.1097A>C	ENSP00000342510.3:p.Asn366Thr
ENST00000467655.1:c.712A>C	ENSP00000418547.1:n.712A>C
ENST00000489172.5:n.1079A>C
ENST00000494050.5:c.1028-108A>C	ENSP00000418185.1:n.1028-108A>C
NM_001303401.1:c.1028-108A>C	NP_001290330.1:n.1028-108A>C
NM_024548.3:c.1097A>C	NP_078824.2:p.Asn366Thr
XM_006713743.2:c.995A>C	XP_006713806.1:p.Asn332Thr
XM_011513125.1:c.881A>C	XP_011511427.1:p.Asn294Thr
XM_011513126.1:c.881A>C	XP_011511428.1:p.Asn294Thr
XM_011513127.1:c.749A>C	XP_011511429.1:p.Asn250Thr
XM_006713743.4:c.995A>C	XP_006713806.1:p.Asn332Thr
XM_017007178.2:c.926-108A>C	XP_016862667.1:n.926-108A>C
NM_024548.4:c.1097A>C MANE Select	NP_078824.2:p.Asn366Thr
NM_001303401.2:c.1028-108A>C	NP_001290330.1:n.1028-108A>C