Canonical Allele Identifier: CA1388867379

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757698T= , CM000665.2:g.101757698T=	GRCh38
NC_000003.11:g.101476542T= , CM000665.1:g.101476542T=	GRCh37
NC_000003.10:g.102959232T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*727T=	ENSP00000419009.1:n.*727T=
ENST00000467655.2:c.*179T=	ENSP00000418547.2:n.*179T=
ENST00000704365.1:c.1092T=	ENSP00000515873.1:p.Val364=
ENST00000704366.1:c.990T=	ENSP00000515874.1:p.Val330=
ENST00000704367.1:c.926-113T=	ENSP00000515875.1:n.926-113T=
ENST00000704368.1:n.1585T=
ENST00000704369.1:c.606T=	ENSP00000515876.1:p.Val202=
ENST00000704370.1:c.1086T=	ENSP00000515877.1:p.Val362=
ENST00000704372.1:n.1446T=
ENST00000704444.1:c.876T=	ENSP00000515896.1:p.Val292=
ENST00000704445.1:c.744T=	ENSP00000515897.1:p.Val248=
ENST00000704446.1:c.1048+502T=	ENSP00000515898.1:n.1048+502T=
ENST00000341893.8:c.1092T= MANE Select	ENSP00000342510.3:p.Val364=
ENST00000341893.7:c.1092T=	ENSP00000342510.3:p.Val364=
ENST00000467655.1:c.707T=	ENSP00000418547.1:n.707T=
ENST00000489172.5:n.1074T=
ENST00000494050.5:c.1028-113T=	ENSP00000418185.1:n.1028-113T=
NM_001303401.1:c.1028-113T=	NP_001290330.1:n.1028-113T=
NM_024548.3:c.1092T=	NP_078824.2:p.Val364=
XM_006713743.2:c.990T=	XP_006713806.1:p.Val330=
XM_011513125.1:c.876T=	XP_011511427.1:p.Val292=
XM_011513126.1:c.876T=	XP_011511428.1:p.Val292=
XM_011513127.1:c.744T=	XP_011511429.1:p.Val248=
XM_006713743.4:c.990T=	XP_006713806.1:p.Val330=
XM_017007178.2:c.926-113T=	XP_016862667.1:n.926-113T=
NM_024548.4:c.1092T= MANE Select	NP_078824.2:p.Val364=
NM_001303401.2:c.1028-113T=	NP_001290330.1:n.1028-113T=