Canonical Allele Identifier: CA1388867444

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757844C= , CM000665.2:g.101757844C=	GRCh38
NC_000003.11:g.101476688C= , CM000665.1:g.101476688C=	GRCh37
NC_000003.10:g.102959378C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*873C=	ENSP00000419009.1:n.*873C=
ENST00000467655.2:c.*325C=	ENSP00000418547.2:n.*325C=
ENST00000704365.1:c.1238C=	ENSP00000515873.1:p.Ser413=
ENST00000704366.1:c.1136C=	ENSP00000515874.1:p.Ser379=
ENST00000704367.1:c.959C=	ENSP00000515875.1:p.Ser320=
ENST00000704368.1:n.1731C=
ENST00000704369.1:c.752C=	ENSP00000515876.1:p.Ser251=
ENST00000704370.1:c.1232C=	ENSP00000515877.1:p.Ser411=
ENST00000704372.1:n.1592C=
ENST00000704444.1:c.1022C=	ENSP00000515896.1:p.Ser341=
ENST00000704445.1:c.890C=	ENSP00000515897.1:p.Ser297=
ENST00000704446.1:c.1048+648C=	ENSP00000515898.1:n.1048+648C=
ENST00000341893.8:c.1238C= MANE Select	ENSP00000342510.3:p.Ser413=
ENST00000341893.7:c.1238C=	ENSP00000342510.3:p.Ser413=
ENST00000467655.1:c.853C=	ENSP00000418547.1:n.853C=
ENST00000489172.5:n.1220C=
ENST00000494050.5:c.1061C=	ENSP00000418185.1:p.Ser354=
NM_001303401.1:c.1061C=	NP_001290330.1:p.Ser354=
NM_024548.3:c.1238C=	NP_078824.2:p.Ser413=
XM_006713743.2:c.1136C=	XP_006713806.1:p.Ser379=
XM_011513125.1:c.1022C=	XP_011511427.1:p.Ser341=
XM_011513126.1:c.1022C=	XP_011511428.1:p.Ser341=
XM_011513127.1:c.890C=	XP_011511429.1:p.Ser297=
XM_006713743.4:c.1136C=	XP_006713806.1:p.Ser379=
XM_017007178.2:c.959C=	XP_016862667.1:p.Ser320=
NM_024548.4:c.1238C= MANE Select	NP_078824.2:p.Ser413=
NM_001303401.2:c.1061C=	NP_001290330.1:p.Ser354=