Canonical Allele Identifier: CA434873058

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476971A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758127A>G , CM000665.2:g.101758127A>G	GRCh38
NC_000003.11:g.101476971A>G , CM000665.1:g.101476971A>G	GRCh37
NC_000003.10:g.102959661A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1156A>G	ENSP00000419009.1:n.*1156A>G
ENST00000467655.2:c.*608A>G	ENSP00000418547.2:n.*608A>G
ENST00000704365.1:c.1521A>G	ENSP00000515873.1:p.Ser507=
ENST00000704366.1:c.1419A>G	ENSP00000515874.1:p.Ser473=
ENST00000704367.1:c.1242A>G	ENSP00000515875.1:p.Ser414=
ENST00000704368.1:n.2014A>G
ENST00000704369.1:c.1035A>G	ENSP00000515876.1:p.Ser345=
ENST00000704370.1:c.1515A>G	ENSP00000515877.1:p.Ser505=
ENST00000704372.1:n.1875A>G
ENST00000704444.1:c.1305A>G	ENSP00000515896.1:p.Ser435=
ENST00000704445.1:c.1173A>G	ENSP00000515897.1:p.Ser391=
ENST00000704446.1:c.1048+931A>G	ENSP00000515898.1:n.1048+931A>G
ENST00000341893.8:c.1521A>G MANE Select	ENSP00000342510.3:p.Ser507=
ENST00000341893.7:c.1521A>G	ENSP00000342510.3:p.Ser507=
ENST00000467655.1:c.1136A>G	ENSP00000418547.1:n.1136A>G
ENST00000489172.5:n.1503A>G
ENST00000494050.5:c.1344A>G	ENSP00000418185.1:p.Ser448=
NM_001303401.1:c.1344A>G	NP_001290330.1:p.Ser448=
NM_024548.3:c.1521A>G	NP_078824.2:p.Ser507=
XM_006713743.2:c.1419A>G	XP_006713806.1:p.Ser473=
XM_011513125.1:c.1305A>G	XP_011511427.1:p.Ser435=
XM_011513126.1:c.1305A>G	XP_011511428.1:p.Ser435=
XM_011513127.1:c.1173A>G	XP_011511429.1:p.Ser391=
XM_006713743.4:c.1419A>G	XP_006713806.1:p.Ser473=
XM_017007178.2:c.1242A>G	XP_016862667.1:p.Ser414=
NM_024548.4:c.1521A>G MANE Select	NP_078824.2:p.Ser507=
NM_001303401.2:c.1344A>G	NP_001290330.1:p.Ser448=