Canonical Allele Identifier: CA1388867372

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757685A= , CM000665.2:g.101757685A=	GRCh38
NC_000003.11:g.101476529A= , CM000665.1:g.101476529A=	GRCh37
NC_000003.10:g.102959219A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*714A=	ENSP00000419009.1:n.*714A=
ENST00000467655.2:c.*166A=	ENSP00000418547.2:n.*166A=
ENST00000704365.1:c.1079A=	ENSP00000515873.1:p.Gln360=
ENST00000704366.1:c.977A=	ENSP00000515874.1:p.Gln326=
ENST00000704367.1:c.926-126A=	ENSP00000515875.1:n.926-126A=
ENST00000704368.1:n.1572A=
ENST00000704369.1:c.593A=	ENSP00000515876.1:p.Gln198=
ENST00000704370.1:c.1073A=	ENSP00000515877.1:p.Gln358=
ENST00000704372.1:n.1433A=
ENST00000704444.1:c.863A=	ENSP00000515896.1:p.Gln288=
ENST00000704445.1:c.731A=	ENSP00000515897.1:p.Gln244=
ENST00000704446.1:c.1048+489A=	ENSP00000515898.1:n.1048+489A=
ENST00000341893.8:c.1079A= MANE Select	ENSP00000342510.3:p.Gln360=
ENST00000341893.7:c.1079A=	ENSP00000342510.3:p.Gln360=
ENST00000467655.1:c.694A=	ENSP00000418547.1:n.694A=
ENST00000489172.5:n.1061A=
ENST00000494050.5:c.1028-126A=	ENSP00000418185.1:n.1028-126A=
NM_001303401.1:c.1028-126A=	NP_001290330.1:n.1028-126A=
NM_024548.3:c.1079A=	NP_078824.2:p.Gln360=
XM_006713743.2:c.977A=	XP_006713806.1:p.Gln326=
XM_011513125.1:c.863A=	XP_011511427.1:p.Gln288=
XM_011513126.1:c.863A=	XP_011511428.1:p.Gln288=
XM_011513127.1:c.731A=	XP_011511429.1:p.Gln244=
XM_006713743.4:c.977A=	XP_006713806.1:p.Gln326=
XM_017007178.2:c.926-126A=	XP_016862667.1:n.926-126A=
NM_024548.4:c.1079A= MANE Select	NP_078824.2:p.Gln360=
NM_001303401.2:c.1028-126A=	NP_001290330.1:n.1028-126A=