Canonical Allele Identifier: CA1388867549

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758138A= , CM000665.2:g.101758138A=	GRCh38
NC_000003.11:g.101476982A= , CM000665.1:g.101476982A=	GRCh37
NC_000003.10:g.102959672A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1167A=	ENSP00000419009.1:n.*1167A=
ENST00000467655.2:c.*619A=	ENSP00000418547.2:n.*619A=
ENST00000704365.1:c.1532A=	ENSP00000515873.1:p.Lys511=
ENST00000704366.1:c.1430A=	ENSP00000515874.1:p.Lys477=
ENST00000704367.1:c.1253A=	ENSP00000515875.1:p.Lys418=
ENST00000704368.1:n.2025A=
ENST00000704369.1:c.1046A=	ENSP00000515876.1:p.Lys349=
ENST00000704370.1:c.1526A=	ENSP00000515877.1:p.Lys509=
ENST00000704372.1:n.1886A=
ENST00000704444.1:c.1316A=	ENSP00000515896.1:p.Lys439=
ENST00000704445.1:c.1184A=	ENSP00000515897.1:p.Lys395=
ENST00000704446.1:c.1048+942A=	ENSP00000515898.1:n.1048+942A=
ENST00000341893.8:c.1532A= MANE Select	ENSP00000342510.3:p.Lys511=
ENST00000341893.7:c.1532A=	ENSP00000342510.3:p.Lys511=
ENST00000467655.1:c.1147A=	ENSP00000418547.1:n.1147A=
ENST00000489172.5:n.1514A=
ENST00000494050.5:c.1355A=	ENSP00000418185.1:p.Lys452=
NM_001303401.1:c.1355A=	NP_001290330.1:p.Lys452=
NM_024548.3:c.1532A=	NP_078824.2:p.Lys511=
XM_006713743.2:c.1430A=	XP_006713806.1:p.Lys477=
XM_011513125.1:c.1316A=	XP_011511427.1:p.Lys439=
XM_011513126.1:c.1316A=	XP_011511428.1:p.Lys439=
XM_011513127.1:c.1184A=	XP_011511429.1:p.Lys395=
XM_006713743.4:c.1430A=	XP_006713806.1:p.Lys477=
XM_017007178.2:c.1253A=	XP_016862667.1:p.Lys418=
NM_024548.4:c.1532A= MANE Select	NP_078824.2:p.Lys511=
NM_001303401.2:c.1355A=	NP_001290330.1:p.Lys452=