Canonical Allele Identifier: CA353875954

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476505T>A (hg19) ; chr3:g.101757661T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757661T>A , CM000665.2:g.101757661T>A	GRCh38
NC_000003.11:g.101476505T>A , CM000665.1:g.101476505T>A	GRCh37
NC_000003.10:g.102959195T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*690T>A	ENSP00000419009.1:n.*690T>A
ENST00000467655.2:c.*142T>A	ENSP00000418547.2:n.*142T>A
ENST00000704365.1:c.1055T>A	ENSP00000515873.1:p.Val352Asp
ENST00000704366.1:c.953T>A	ENSP00000515874.1:p.Val318Asp
ENST00000704367.1:c.926-150T>A	ENSP00000515875.1:n.926-150T>A
ENST00000704368.1:n.1548T>A
ENST00000704369.1:c.569T>A	ENSP00000515876.1:p.Val190Asp
ENST00000704370.1:c.1049T>A	ENSP00000515877.1:p.Val350Asp
ENST00000704372.1:n.1409T>A
ENST00000704444.1:c.839T>A	ENSP00000515896.1:p.Val280Asp
ENST00000704445.1:c.707T>A	ENSP00000515897.1:p.Val236Asp
ENST00000704446.1:c.1048+465T>A	ENSP00000515898.1:n.1048+465T>A
ENST00000341893.8:c.1055T>A MANE Select	ENSP00000342510.3:p.Val352Asp
ENST00000341893.7:c.1055T>A	ENSP00000342510.3:p.Val352Asp
ENST00000467655.1:c.670T>A	ENSP00000418547.1:n.670T>A
ENST00000489172.5:n.1037T>A
ENST00000494050.5:c.1028-150T>A	ENSP00000418185.1:n.1028-150T>A
NM_001303401.1:c.1028-150T>A	NP_001290330.1:n.1028-150T>A
NM_024548.3:c.1055T>A	NP_078824.2:p.Val352Asp
XM_006713743.2:c.953T>A	XP_006713806.1:p.Val318Asp
XM_011513125.1:c.839T>A	XP_011511427.1:p.Val280Asp
XM_011513126.1:c.839T>A	XP_011511428.1:p.Val280Asp
XM_011513127.1:c.707T>A	XP_011511429.1:p.Val236Asp
XM_006713743.4:c.953T>A	XP_006713806.1:p.Val318Asp
XM_017007178.2:c.926-150T>A	XP_016862667.1:n.926-150T>A
NM_024548.4:c.1055T>A MANE Select	NP_078824.2:p.Val352Asp
NM_001303401.2:c.1028-150T>A	NP_001290330.1:n.1028-150T>A