Canonical Allele Identifier: CA1388867374

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757686G= , CM000665.2:g.101757686G=	GRCh38
NC_000003.11:g.101476530G= , CM000665.1:g.101476530G=	GRCh37
NC_000003.10:g.102959220G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*715G=	ENSP00000419009.1:n.*715G=
ENST00000467655.2:c.*167G=	ENSP00000418547.2:n.*167G=
ENST00000704365.1:c.1080G=	ENSP00000515873.1:p.Gln360=
ENST00000704366.1:c.978G=	ENSP00000515874.1:p.Gln326=
ENST00000704367.1:c.926-125G=	ENSP00000515875.1:n.926-125G=
ENST00000704368.1:n.1573G=
ENST00000704369.1:c.594G=	ENSP00000515876.1:p.Gln198=
ENST00000704370.1:c.1074G=	ENSP00000515877.1:p.Gln358=
ENST00000704372.1:n.1434G=
ENST00000704444.1:c.864G=	ENSP00000515896.1:p.Gln288=
ENST00000704445.1:c.732G=	ENSP00000515897.1:p.Gln244=
ENST00000704446.1:c.1048+490G=	ENSP00000515898.1:n.1048+490G=
ENST00000341893.8:c.1080G= MANE Select	ENSP00000342510.3:p.Gln360=
ENST00000341893.7:c.1080G=	ENSP00000342510.3:p.Gln360=
ENST00000467655.1:c.695G=	ENSP00000418547.1:n.695G=
ENST00000489172.5:n.1062G=
ENST00000494050.5:c.1028-125G=	ENSP00000418185.1:n.1028-125G=
NM_001303401.1:c.1028-125G=	NP_001290330.1:n.1028-125G=
NM_024548.3:c.1080G=	NP_078824.2:p.Gln360=
XM_006713743.2:c.978G=	XP_006713806.1:p.Gln326=
XM_011513125.1:c.864G=	XP_011511427.1:p.Gln288=
XM_011513126.1:c.864G=	XP_011511428.1:p.Gln288=
XM_011513127.1:c.732G=	XP_011511429.1:p.Gln244=
XM_006713743.4:c.978G=	XP_006713806.1:p.Gln326=
XM_017007178.2:c.926-125G=	XP_016862667.1:n.926-125G=
NM_024548.4:c.1080G= MANE Select	NP_078824.2:p.Gln360=
NM_001303401.2:c.1028-125G=	NP_001290330.1:n.1028-125G=