Canonical Allele Identifier: CA434873426

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476917A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758073A>C , CM000665.2:g.101758073A>C	GRCh38
NC_000003.11:g.101476917A>C , CM000665.1:g.101476917A>C	GRCh37
NC_000003.10:g.102959607A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1102A>C	ENSP00000419009.1:n.*1102A>C
ENST00000467655.2:c.*554A>C	ENSP00000418547.2:n.*554A>C
ENST00000704365.1:c.1467A>C	ENSP00000515873.1:p.Ile489=
ENST00000704366.1:c.1365A>C	ENSP00000515874.1:p.Ile455=
ENST00000704367.1:c.1188A>C	ENSP00000515875.1:p.Ile396=
ENST00000704368.1:n.1960A>C
ENST00000704369.1:c.981A>C	ENSP00000515876.1:p.Ile327=
ENST00000704370.1:c.1461A>C	ENSP00000515877.1:p.Ile487=
ENST00000704372.1:n.1821A>C
ENST00000704444.1:c.1251A>C	ENSP00000515896.1:p.Ile417=
ENST00000704445.1:c.1119A>C	ENSP00000515897.1:p.Ile373=
ENST00000704446.1:c.1048+877A>C	ENSP00000515898.1:n.1048+877A>C
ENST00000341893.8:c.1467A>C MANE Select	ENSP00000342510.3:p.Ile489=
ENST00000341893.7:c.1467A>C	ENSP00000342510.3:p.Ile489=
ENST00000467655.1:c.1082A>C	ENSP00000418547.1:n.1082A>C
ENST00000489172.5:n.1449A>C
ENST00000494050.5:c.1290A>C	ENSP00000418185.1:p.Ile430=
NM_001303401.1:c.1290A>C	NP_001290330.1:p.Ile430=
NM_024548.3:c.1467A>C	NP_078824.2:p.Ile489=
XM_006713743.2:c.1365A>C	XP_006713806.1:p.Ile455=
XM_011513125.1:c.1251A>C	XP_011511427.1:p.Ile417=
XM_011513126.1:c.1251A>C	XP_011511428.1:p.Ile417=
XM_011513127.1:c.1119A>C	XP_011511429.1:p.Ile373=
XM_006713743.4:c.1365A>C	XP_006713806.1:p.Ile455=
XM_017007178.2:c.1188A>C	XP_016862667.1:p.Ile396=
NM_024548.4:c.1467A>C MANE Select	NP_078824.2:p.Ile489=
NM_001303401.2:c.1290A>C	NP_001290330.1:p.Ile430=