Canonical Allele Identifier: CA1388867535

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758096A= , CM000665.2:g.101758096A=	GRCh38
NC_000003.11:g.101476940A= , CM000665.1:g.101476940A=	GRCh37
NC_000003.10:g.102959630A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1125A=	ENSP00000419009.1:n.*1125A=
ENST00000467655.2:c.*577A=	ENSP00000418547.2:n.*577A=
ENST00000704365.1:c.1490A=	ENSP00000515873.1:p.Asp497=
ENST00000704366.1:c.1388A=	ENSP00000515874.1:p.Asp463=
ENST00000704367.1:c.1211A=	ENSP00000515875.1:p.Asp404=
ENST00000704368.1:n.1983A=
ENST00000704369.1:c.1004A=	ENSP00000515876.1:p.Asp335=
ENST00000704370.1:c.1484A=	ENSP00000515877.1:p.Asp495=
ENST00000704372.1:n.1844A=
ENST00000704444.1:c.1274A=	ENSP00000515896.1:p.Asp425=
ENST00000704445.1:c.1142A=	ENSP00000515897.1:p.Asp381=
ENST00000704446.1:c.1048+900A=	ENSP00000515898.1:n.1048+900A=
ENST00000341893.8:c.1490A= MANE Select	ENSP00000342510.3:p.Asp497=
ENST00000341893.7:c.1490A=	ENSP00000342510.3:p.Asp497=
ENST00000467655.1:c.1105A=	ENSP00000418547.1:n.1105A=
ENST00000489172.5:n.1472A=
ENST00000494050.5:c.1313A=	ENSP00000418185.1:p.Asp438=
NM_001303401.1:c.1313A=	NP_001290330.1:p.Asp438=
NM_024548.3:c.1490A=	NP_078824.2:p.Asp497=
XM_006713743.2:c.1388A=	XP_006713806.1:p.Asp463=
XM_011513125.1:c.1274A=	XP_011511427.1:p.Asp425=
XM_011513126.1:c.1274A=	XP_011511428.1:p.Asp425=
XM_011513127.1:c.1142A=	XP_011511429.1:p.Asp381=
XM_006713743.4:c.1388A=	XP_006713806.1:p.Asp463=
XM_017007178.2:c.1211A=	XP_016862667.1:p.Asp404=
NM_024548.4:c.1490A= MANE Select	NP_078824.2:p.Asp497=
NM_001303401.2:c.1313A=	NP_001290330.1:p.Asp438=