Canonical Allele Identifier: CA353876966

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476665T>A (hg19) ; chr3:g.101757821T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757821T>A , CM000665.2:g.101757821T>A	GRCh38
NC_000003.11:g.101476665T>A , CM000665.1:g.101476665T>A	GRCh37
NC_000003.10:g.102959355T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*850T>A	ENSP00000419009.1:n.*850T>A
ENST00000467655.2:c.*302T>A	ENSP00000418547.2:n.*302T>A
ENST00000704365.1:c.1215T>A	ENSP00000515873.1:p.Phe405Leu
ENST00000704366.1:c.1113T>A	ENSP00000515874.1:p.Phe371Leu
ENST00000704367.1:c.936T>A	ENSP00000515875.1:p.Phe312Leu
ENST00000704368.1:n.1708T>A
ENST00000704369.1:c.729T>A	ENSP00000515876.1:p.Phe243Leu
ENST00000704370.1:c.1209T>A	ENSP00000515877.1:p.Phe403Leu
ENST00000704372.1:n.1569T>A
ENST00000704444.1:c.999T>A	ENSP00000515896.1:p.Phe333Leu
ENST00000704445.1:c.867T>A	ENSP00000515897.1:p.Phe289Leu
ENST00000704446.1:c.1048+625T>A	ENSP00000515898.1:n.1048+625T>A
ENST00000341893.8:c.1215T>A MANE Select	ENSP00000342510.3:p.Phe405Leu
ENST00000341893.7:c.1215T>A	ENSP00000342510.3:p.Phe405Leu
ENST00000467655.1:c.830T>A	ENSP00000418547.1:n.830T>A
ENST00000489172.5:n.1197T>A
ENST00000494050.5:c.1038T>A	ENSP00000418185.1:p.Phe346Leu
NM_001303401.1:c.1038T>A	NP_001290330.1:p.Phe346Leu
NM_024548.3:c.1215T>A	NP_078824.2:p.Phe405Leu
XM_006713743.2:c.1113T>A	XP_006713806.1:p.Phe371Leu
XM_011513125.1:c.999T>A	XP_011511427.1:p.Phe333Leu
XM_011513126.1:c.999T>A	XP_011511428.1:p.Phe333Leu
XM_011513127.1:c.867T>A	XP_011511429.1:p.Phe289Leu
XM_006713743.4:c.1113T>A	XP_006713806.1:p.Phe371Leu
XM_017007178.2:c.936T>A	XP_016862667.1:p.Phe312Leu
NM_024548.4:c.1215T>A MANE Select	NP_078824.2:p.Phe405Leu
NM_001303401.2:c.1038T>A	NP_001290330.1:p.Phe346Leu