Canonical Allele Identifier: CA1388867547

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758134C= , CM000665.2:g.101758134C=	GRCh38
NC_000003.11:g.101476978C= , CM000665.1:g.101476978C=	GRCh37
NC_000003.10:g.102959668C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1163C=	ENSP00000419009.1:n.*1163C=
ENST00000467655.2:c.*615C=	ENSP00000418547.2:n.*615C=
ENST00000704365.1:c.1528C=	ENSP00000515873.1:p.Gln510=
ENST00000704366.1:c.1426C=	ENSP00000515874.1:p.Gln476=
ENST00000704367.1:c.1249C=	ENSP00000515875.1:p.Gln417=
ENST00000704368.1:n.2021C=
ENST00000704369.1:c.1042C=	ENSP00000515876.1:p.Gln348=
ENST00000704370.1:c.1522C=	ENSP00000515877.1:p.Gln508=
ENST00000704372.1:n.1882C=
ENST00000704444.1:c.1312C=	ENSP00000515896.1:p.Gln438=
ENST00000704445.1:c.1180C=	ENSP00000515897.1:p.Gln394=
ENST00000704446.1:c.1048+938C=	ENSP00000515898.1:n.1048+938C=
ENST00000341893.8:c.1528C= MANE Select	ENSP00000342510.3:p.Gln510=
ENST00000341893.7:c.1528C=	ENSP00000342510.3:p.Gln510=
ENST00000467655.1:c.1143C=	ENSP00000418547.1:n.1143C=
ENST00000489172.5:n.1510C=
ENST00000494050.5:c.1351C=	ENSP00000418185.1:p.Gln451=
NM_001303401.1:c.1351C=	NP_001290330.1:p.Gln451=
NM_024548.3:c.1528C=	NP_078824.2:p.Gln510=
XM_006713743.2:c.1426C=	XP_006713806.1:p.Gln476=
XM_011513125.1:c.1312C=	XP_011511427.1:p.Gln438=
XM_011513126.1:c.1312C=	XP_011511428.1:p.Gln438=
XM_011513127.1:c.1180C=	XP_011511429.1:p.Gln394=
XM_006713743.4:c.1426C=	XP_006713806.1:p.Gln476=
XM_017007178.2:c.1249C=	XP_016862667.1:p.Gln417=
NM_024548.4:c.1528C= MANE Select	NP_078824.2:p.Gln510=
NM_001303401.2:c.1351C=	NP_001290330.1:p.Gln451=