Canonical Allele Identifier: CA434873413

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476911A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758067A>C , CM000665.2:g.101758067A>C	GRCh38
NC_000003.11:g.101476911A>C , CM000665.1:g.101476911A>C	GRCh37
NC_000003.10:g.102959601A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1096A>C	ENSP00000419009.1:n.*1096A>C
ENST00000467655.2:c.*548A>C	ENSP00000418547.2:n.*548A>C
ENST00000704365.1:c.1461A>C	ENSP00000515873.1:p.Pro487=
ENST00000704366.1:c.1359A>C	ENSP00000515874.1:p.Pro453=
ENST00000704367.1:c.1182A>C	ENSP00000515875.1:p.Pro394=
ENST00000704368.1:n.1954A>C
ENST00000704369.1:c.975A>C	ENSP00000515876.1:p.Pro325=
ENST00000704370.1:c.1455A>C	ENSP00000515877.1:p.Pro485=
ENST00000704372.1:n.1815A>C
ENST00000704444.1:c.1245A>C	ENSP00000515896.1:p.Pro415=
ENST00000704445.1:c.1113A>C	ENSP00000515897.1:p.Pro371=
ENST00000704446.1:c.1048+871A>C	ENSP00000515898.1:n.1048+871A>C
ENST00000341893.8:c.1461A>C MANE Select	ENSP00000342510.3:p.Pro487=
ENST00000341893.7:c.1461A>C	ENSP00000342510.3:p.Pro487=
ENST00000467655.1:c.1076A>C	ENSP00000418547.1:n.1076A>C
ENST00000489172.5:n.1443A>C
ENST00000494050.5:c.1284A>C	ENSP00000418185.1:p.Pro428=
NM_001303401.1:c.1284A>C	NP_001290330.1:p.Pro428=
NM_024548.3:c.1461A>C	NP_078824.2:p.Pro487=
XM_006713743.2:c.1359A>C	XP_006713806.1:p.Pro453=
XM_011513125.1:c.1245A>C	XP_011511427.1:p.Pro415=
XM_011513126.1:c.1245A>C	XP_011511428.1:p.Pro415=
XM_011513127.1:c.1113A>C	XP_011511429.1:p.Pro371=
XM_006713743.4:c.1359A>C	XP_006713806.1:p.Pro453=
XM_017007178.2:c.1182A>C	XP_016862667.1:p.Pro394=
NM_024548.4:c.1461A>C MANE Select	NP_078824.2:p.Pro487=
NM_001303401.2:c.1284A>C	NP_001290330.1:p.Pro428=