Canonical Allele Identifier: CA1388867478

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757932G= , CM000665.2:g.101757932G=	GRCh38
NC_000003.11:g.101476776G= , CM000665.1:g.101476776G=	GRCh37
NC_000003.10:g.102959466G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*961G=	ENSP00000419009.1:n.*961G=
ENST00000467655.2:c.*413G=	ENSP00000418547.2:n.*413G=
ENST00000704365.1:c.1326G=	ENSP00000515873.1:p.Gly442=
ENST00000704366.1:c.1224G=	ENSP00000515874.1:p.Gly408=
ENST00000704367.1:c.1047G=	ENSP00000515875.1:p.Gly349=
ENST00000704368.1:n.1819G=
ENST00000704369.1:c.840G=	ENSP00000515876.1:p.Gly280=
ENST00000704370.1:c.1320G=	ENSP00000515877.1:p.Gly440=
ENST00000704372.1:n.1680G=
ENST00000704444.1:c.1110G=	ENSP00000515896.1:p.Gly370=
ENST00000704445.1:c.978G=	ENSP00000515897.1:p.Gly326=
ENST00000704446.1:c.1048+736G=	ENSP00000515898.1:n.1048+736G=
ENST00000341893.8:c.1326G= MANE Select	ENSP00000342510.3:p.Gly442=
ENST00000341893.7:c.1326G=	ENSP00000342510.3:p.Gly442=
ENST00000467655.1:c.941G=	ENSP00000418547.1:n.941G=
ENST00000489172.5:n.1308G=
ENST00000494050.5:c.1149G=	ENSP00000418185.1:p.Gly383=
NM_001303401.1:c.1149G=	NP_001290330.1:p.Gly383=
NM_024548.3:c.1326G=	NP_078824.2:p.Gly442=
XM_006713743.2:c.1224G=	XP_006713806.1:p.Gly408=
XM_011513125.1:c.1110G=	XP_011511427.1:p.Gly370=
XM_011513126.1:c.1110G=	XP_011511428.1:p.Gly370=
XM_011513127.1:c.978G=	XP_011511429.1:p.Gly326=
XM_006713743.4:c.1224G=	XP_006713806.1:p.Gly408=
XM_017007178.2:c.1047G=	XP_016862667.1:p.Gly349=
NM_024548.4:c.1326G= MANE Select	NP_078824.2:p.Gly442=
NM_001303401.2:c.1149G=	NP_001290330.1:p.Gly383=