Canonical Allele Identifier: CA434873064

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476974T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758130T>C , CM000665.2:g.101758130T>C	GRCh38
NC_000003.11:g.101476974T>C , CM000665.1:g.101476974T>C	GRCh37
NC_000003.10:g.102959664T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1159T>C	ENSP00000419009.1:n.*1159T>C
ENST00000467655.2:c.*611T>C	ENSP00000418547.2:n.*611T>C
ENST00000704365.1:c.1524T>C	ENSP00000515873.1:p.Thr508=
ENST00000704366.1:c.1422T>C	ENSP00000515874.1:p.Thr474=
ENST00000704367.1:c.1245T>C	ENSP00000515875.1:p.Thr415=
ENST00000704368.1:n.2017T>C
ENST00000704369.1:c.1038T>C	ENSP00000515876.1:p.Thr346=
ENST00000704370.1:c.1518T>C	ENSP00000515877.1:p.Thr506=
ENST00000704372.1:n.1878T>C
ENST00000704444.1:c.1308T>C	ENSP00000515896.1:p.Thr436=
ENST00000704445.1:c.1176T>C	ENSP00000515897.1:p.Thr392=
ENST00000704446.1:c.1048+934T>C	ENSP00000515898.1:n.1048+934T>C
ENST00000341893.8:c.1524T>C MANE Select	ENSP00000342510.3:p.Thr508=
ENST00000341893.7:c.1524T>C	ENSP00000342510.3:p.Thr508=
ENST00000467655.1:c.1139T>C	ENSP00000418547.1:n.1139T>C
ENST00000489172.5:n.1506T>C
ENST00000494050.5:c.1347T>C	ENSP00000418185.1:p.Thr449=
NM_001303401.1:c.1347T>C	NP_001290330.1:p.Thr449=
NM_024548.3:c.1524T>C	NP_078824.2:p.Thr508=
XM_006713743.2:c.1422T>C	XP_006713806.1:p.Thr474=
XM_011513125.1:c.1308T>C	XP_011511427.1:p.Thr436=
XM_011513126.1:c.1308T>C	XP_011511428.1:p.Thr436=
XM_011513127.1:c.1176T>C	XP_011511429.1:p.Thr392=
XM_006713743.4:c.1422T>C	XP_006713806.1:p.Thr474=
XM_017007178.2:c.1245T>C	XP_016862667.1:p.Thr415=
NM_024548.4:c.1524T>C MANE Select	NP_078824.2:p.Thr508=
NM_001303401.2:c.1347T>C	NP_001290330.1:p.Thr449=