Canonical Allele Identifier: CA353877832

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476996A>T (hg19) ; chr3:g.101758152A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758152A>T , CM000665.2:g.101758152A>T	GRCh38
NC_000003.11:g.101476996A>T , CM000665.1:g.101476996A>T	GRCh37
NC_000003.10:g.102959686A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1181A>T	ENSP00000419009.1:n.*1181A>T
ENST00000467655.2:c.*633A>T	ENSP00000418547.2:n.*633A>T
ENST00000704365.1:c.1546A>T	ENSP00000515873.1:p.Lys516Ter
ENST00000704366.1:c.1444A>T	ENSP00000515874.1:p.Lys482Ter
ENST00000704367.1:c.1267A>T	ENSP00000515875.1:p.Lys423Ter
ENST00000704368.1:n.2039A>T
ENST00000704369.1:c.1060A>T	ENSP00000515876.1:p.Lys354Ter
ENST00000704370.1:c.1540A>T	ENSP00000515877.1:p.Lys514Ter
ENST00000704372.1:n.1900A>T
ENST00000704444.1:c.1330A>T	ENSP00000515896.1:p.Lys444Ter
ENST00000704445.1:c.1198A>T	ENSP00000515897.1:p.Lys400Ter
ENST00000704446.1:c.1048+956A>T	ENSP00000515898.1:n.1048+956A>T
ENST00000341893.8:c.1546A>T MANE Select	ENSP00000342510.3:p.Lys516Ter
ENST00000341893.7:c.1546A>T	ENSP00000342510.3:p.Lys516Ter
ENST00000467655.1:c.1161A>T	ENSP00000418547.1:n.1161A>T
ENST00000489172.5:n.1528A>T
ENST00000494050.5:c.1369A>T	ENSP00000418185.1:p.Lys457Ter
NM_001303401.1:c.1369A>T	NP_001290330.1:p.Lys457Ter
NM_024548.3:c.1546A>T	NP_078824.2:p.Lys516Ter
XM_006713743.2:c.1444A>T	XP_006713806.1:p.Lys482Ter
XM_011513125.1:c.1330A>T	XP_011511427.1:p.Lys444Ter
XM_011513126.1:c.1330A>T	XP_011511428.1:p.Lys444Ter
XM_011513127.1:c.1198A>T	XP_011511429.1:p.Lys400Ter
XM_006713743.4:c.1444A>T	XP_006713806.1:p.Lys482Ter
XM_017007178.2:c.1267A>T	XP_016862667.1:p.Lys423Ter
NM_024548.4:c.1546A>T MANE Select	NP_078824.2:p.Lys516Ter
NM_001303401.2:c.1369A>T	NP_001290330.1:p.Lys457Ter