Canonical Allele Identifier: CA79768639

Gene: CEP97

Linked Data

• dbSNP Id: rs998090865
• gnomAD v2: 3-101476582-T-G
• gnomAD v3: 3-101757738-T-G
• gnomAD v4: 3-101757738-T-G
• MyVariant Identifiers: chr3:g.101476582T>G (hg19) ; chr3:g.101757738T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757738T>G , CM000665.2:g.101757738T>G	GRCh38
NC_000003.11:g.101476582T>G , CM000665.1:g.101476582T>G	GRCh37
NC_000003.10:g.102959272T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*767T>G	ENSP00000419009.1:n.*767T>G
ENST00000467655.2:c.*219T>G	ENSP00000418547.2:n.*219T>G
ENST00000704365.1:c.1132T>G	ENSP00000515873.1:p.Ser378Ala
ENST00000704366.1:c.1030T>G	ENSP00000515874.1:p.Ser344Ala
ENST00000704367.1:c.926-73T>G	ENSP00000515875.1:n.926-73T>G
ENST00000704368.1:n.1625T>G
ENST00000704369.1:c.646T>G	ENSP00000515876.1:p.Ser216Ala
ENST00000704370.1:c.1126T>G	ENSP00000515877.1:p.Ser376Ala
ENST00000704372.1:n.1486T>G
ENST00000704444.1:c.916T>G	ENSP00000515896.1:p.Ser306Ala
ENST00000704445.1:c.784T>G	ENSP00000515897.1:p.Ser262Ala
ENST00000704446.1:c.1048+542T>G	ENSP00000515898.1:n.1048+542T>G
ENST00000341893.8:c.1132T>G MANE Select	ENSP00000342510.3:p.Ser378Ala
ENST00000341893.7:c.1132T>G	ENSP00000342510.3:p.Ser378Ala
ENST00000467655.1:c.747T>G	ENSP00000418547.1:n.747T>G
ENST00000489172.5:n.1114T>G
ENST00000494050.5:c.1028-73T>G	ENSP00000418185.1:n.1028-73T>G
NM_001303401.1:c.1028-73T>G	NP_001290330.1:n.1028-73T>G
NM_024548.3:c.1132T>G	NP_078824.2:p.Ser378Ala
XM_006713743.2:c.1030T>G	XP_006713806.1:p.Ser344Ala
XM_011513125.1:c.916T>G	XP_011511427.1:p.Ser306Ala
XM_011513126.1:c.916T>G	XP_011511428.1:p.Ser306Ala
XM_011513127.1:c.784T>G	XP_011511429.1:p.Ser262Ala
XM_006713743.4:c.1030T>G	XP_006713806.1:p.Ser344Ala
XM_017007178.2:c.926-73T>G	XP_016862667.1:n.926-73T>G
NM_024548.4:c.1132T>G MANE Select	NP_078824.2:p.Ser378Ala
NM_001303401.2:c.1028-73T>G	NP_001290330.1:n.1028-73T>G