Canonical Allele Identifier: CA353877586

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476885G>T (hg19) ; chr3:g.101758041G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758041G>T , CM000665.2:g.101758041G>T	GRCh38
NC_000003.11:g.101476885G>T , CM000665.1:g.101476885G>T	GRCh37
NC_000003.10:g.102959575G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1070G>T	ENSP00000419009.1:n.*1070G>T
ENST00000467655.2:c.*522G>T	ENSP00000418547.2:n.*522G>T
ENST00000704365.1:c.1435G>T	ENSP00000515873.1:p.Ala479Ser
ENST00000704366.1:c.1333G>T	ENSP00000515874.1:p.Ala445Ser
ENST00000704367.1:c.1156G>T	ENSP00000515875.1:p.Ala386Ser
ENST00000704368.1:n.1928G>T
ENST00000704369.1:c.949G>T	ENSP00000515876.1:p.Ala317Ser
ENST00000704370.1:c.1429G>T	ENSP00000515877.1:p.Ala477Ser
ENST00000704372.1:n.1789G>T
ENST00000704444.1:c.1219G>T	ENSP00000515896.1:p.Ala407Ser
ENST00000704445.1:c.1087G>T	ENSP00000515897.1:p.Ala363Ser
ENST00000704446.1:c.1048+845G>T	ENSP00000515898.1:n.1048+845G>T
ENST00000341893.8:c.1435G>T MANE Select	ENSP00000342510.3:p.Ala479Ser
ENST00000341893.7:c.1435G>T	ENSP00000342510.3:p.Ala479Ser
ENST00000467655.1:c.1050G>T	ENSP00000418547.1:n.1050G>T
ENST00000489172.5:n.1417G>T
ENST00000494050.5:c.1258G>T	ENSP00000418185.1:p.Ala420Ser
NM_001303401.1:c.1258G>T	NP_001290330.1:p.Ala420Ser
NM_024548.3:c.1435G>T	NP_078824.2:p.Ala479Ser
XM_006713743.2:c.1333G>T	XP_006713806.1:p.Ala445Ser
XM_011513125.1:c.1219G>T	XP_011511427.1:p.Ala407Ser
XM_011513126.1:c.1219G>T	XP_011511428.1:p.Ala407Ser
XM_011513127.1:c.1087G>T	XP_011511429.1:p.Ala363Ser
XM_006713743.4:c.1333G>T	XP_006713806.1:p.Ala445Ser
XM_017007178.2:c.1156G>T	XP_016862667.1:p.Ala386Ser
NM_024548.4:c.1435G>T MANE Select	NP_078824.2:p.Ala479Ser
NM_001303401.2:c.1258G>T	NP_001290330.1:p.Ala420Ser