Canonical Allele Identifier: CA353877793

Gene: CEP97

Linked Data

• gnomAD v4: 3-101758135-A-G
• MyVariant Identifiers: chr3:g.101476979A>G (hg19) ; chr3:g.101758135A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758135A>G , CM000665.2:g.101758135A>G	GRCh38
NC_000003.11:g.101476979A>G , CM000665.1:g.101476979A>G	GRCh37
NC_000003.10:g.102959669A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1164A>G	ENSP00000419009.1:n.*1164A>G
ENST00000467655.2:c.*616A>G	ENSP00000418547.2:n.*616A>G
ENST00000704365.1:c.1529A>G	ENSP00000515873.1:p.Gln510Arg
ENST00000704366.1:c.1427A>G	ENSP00000515874.1:p.Gln476Arg
ENST00000704367.1:c.1250A>G	ENSP00000515875.1:p.Gln417Arg
ENST00000704368.1:n.2022A>G
ENST00000704369.1:c.1043A>G	ENSP00000515876.1:p.Gln348Arg
ENST00000704370.1:c.1523A>G	ENSP00000515877.1:p.Gln508Arg
ENST00000704372.1:n.1883A>G
ENST00000704444.1:c.1313A>G	ENSP00000515896.1:p.Gln438Arg
ENST00000704445.1:c.1181A>G	ENSP00000515897.1:p.Gln394Arg
ENST00000704446.1:c.1048+939A>G	ENSP00000515898.1:n.1048+939A>G
ENST00000341893.8:c.1529A>G MANE Select	ENSP00000342510.3:p.Gln510Arg
ENST00000341893.7:c.1529A>G	ENSP00000342510.3:p.Gln510Arg
ENST00000467655.1:c.1144A>G	ENSP00000418547.1:n.1144A>G
ENST00000489172.5:n.1511A>G
ENST00000494050.5:c.1352A>G	ENSP00000418185.1:p.Gln451Arg
NM_001303401.1:c.1352A>G	NP_001290330.1:p.Gln451Arg
NM_024548.3:c.1529A>G	NP_078824.2:p.Gln510Arg
XM_006713743.2:c.1427A>G	XP_006713806.1:p.Gln476Arg
XM_011513125.1:c.1313A>G	XP_011511427.1:p.Gln438Arg
XM_011513126.1:c.1313A>G	XP_011511428.1:p.Gln438Arg
XM_011513127.1:c.1181A>G	XP_011511429.1:p.Gln394Arg
XM_006713743.4:c.1427A>G	XP_006713806.1:p.Gln476Arg
XM_017007178.2:c.1250A>G	XP_016862667.1:p.Gln417Arg
NM_024548.4:c.1529A>G MANE Select	NP_078824.2:p.Gln510Arg
NM_001303401.2:c.1352A>G	NP_001290330.1:p.Gln451Arg