Canonical Allele Identifier: CA434873083

Gene: CEP97

Linked Data

• gnomAD v4: 3-101758142-A-G
• MyVariant Identifiers: chr3:g.101476986A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758142A>G , CM000665.2:g.101758142A>G	GRCh38
NC_000003.11:g.101476986A>G , CM000665.1:g.101476986A>G	GRCh37
NC_000003.10:g.102959676A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1171A>G	ENSP00000419009.1:n.*1171A>G
ENST00000467655.2:c.*623A>G	ENSP00000418547.2:n.*623A>G
ENST00000704365.1:c.1536A>G	ENSP00000515873.1:p.Gln512=
ENST00000704366.1:c.1434A>G	ENSP00000515874.1:p.Gln478=
ENST00000704367.1:c.1257A>G	ENSP00000515875.1:p.Gln419=
ENST00000704368.1:n.2029A>G
ENST00000704369.1:c.1050A>G	ENSP00000515876.1:p.Gln350=
ENST00000704370.1:c.1530A>G	ENSP00000515877.1:p.Gln510=
ENST00000704372.1:n.1890A>G
ENST00000704444.1:c.1320A>G	ENSP00000515896.1:p.Gln440=
ENST00000704445.1:c.1188A>G	ENSP00000515897.1:p.Gln396=
ENST00000704446.1:c.1048+946A>G	ENSP00000515898.1:n.1048+946A>G
ENST00000341893.8:c.1536A>G MANE Select	ENSP00000342510.3:p.Gln512=
ENST00000341893.7:c.1536A>G	ENSP00000342510.3:p.Gln512=
ENST00000467655.1:c.1151A>G	ENSP00000418547.1:n.1151A>G
ENST00000489172.5:n.1518A>G
ENST00000494050.5:c.1359A>G	ENSP00000418185.1:p.Gln453=
NM_001303401.1:c.1359A>G	NP_001290330.1:p.Gln453=
NM_024548.3:c.1536A>G	NP_078824.2:p.Gln512=
XM_006713743.2:c.1434A>G	XP_006713806.1:p.Gln478=
XM_011513125.1:c.1320A>G	XP_011511427.1:p.Gln440=
XM_011513126.1:c.1320A>G	XP_011511428.1:p.Gln440=
XM_011513127.1:c.1188A>G	XP_011511429.1:p.Gln396=
XM_006713743.4:c.1434A>G	XP_006713806.1:p.Gln478=
XM_017007178.2:c.1257A>G	XP_016862667.1:p.Gln419=
NM_024548.4:c.1536A>G MANE Select	NP_078824.2:p.Gln512=
NM_001303401.2:c.1359A>G	NP_001290330.1:p.Gln453=