Canonical Allele Identifier: CA434873071

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476980G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758136G>A , CM000665.2:g.101758136G>A	GRCh38
NC_000003.11:g.101476980G>A , CM000665.1:g.101476980G>A	GRCh37
NC_000003.10:g.102959670G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1165G>A	ENSP00000419009.1:n.*1165G>A
ENST00000467655.2:c.*617G>A	ENSP00000418547.2:n.*617G>A
ENST00000704365.1:c.1530G>A	ENSP00000515873.1:p.Gln510=
ENST00000704366.1:c.1428G>A	ENSP00000515874.1:p.Gln476=
ENST00000704367.1:c.1251G>A	ENSP00000515875.1:p.Gln417=
ENST00000704368.1:n.2023G>A
ENST00000704369.1:c.1044G>A	ENSP00000515876.1:p.Gln348=
ENST00000704370.1:c.1524G>A	ENSP00000515877.1:p.Gln508=
ENST00000704372.1:n.1884G>A
ENST00000704444.1:c.1314G>A	ENSP00000515896.1:p.Gln438=
ENST00000704445.1:c.1182G>A	ENSP00000515897.1:p.Gln394=
ENST00000704446.1:c.1048+940G>A	ENSP00000515898.1:n.1048+940G>A
ENST00000341893.8:c.1530G>A MANE Select	ENSP00000342510.3:p.Gln510=
ENST00000341893.7:c.1530G>A	ENSP00000342510.3:p.Gln510=
ENST00000467655.1:c.1145G>A	ENSP00000418547.1:n.1145G>A
ENST00000489172.5:n.1512G>A
ENST00000494050.5:c.1353G>A	ENSP00000418185.1:p.Gln451=
NM_001303401.1:c.1353G>A	NP_001290330.1:p.Gln451=
NM_024548.3:c.1530G>A	NP_078824.2:p.Gln510=
XM_006713743.2:c.1428G>A	XP_006713806.1:p.Gln476=
XM_011513125.1:c.1314G>A	XP_011511427.1:p.Gln438=
XM_011513126.1:c.1314G>A	XP_011511428.1:p.Gln438=
XM_011513127.1:c.1182G>A	XP_011511429.1:p.Gln394=
XM_006713743.4:c.1428G>A	XP_006713806.1:p.Gln476=
XM_017007178.2:c.1251G>A	XP_016862667.1:p.Gln417=
NM_024548.4:c.1530G>A MANE Select	NP_078824.2:p.Gln510=
NM_001303401.2:c.1353G>A	NP_001290330.1:p.Gln451=