Canonical Allele Identifier: CA353877821

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476991A>C (hg19) ; chr3:g.101758147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758147A>C , CM000665.2:g.101758147A>C	GRCh38
NC_000003.11:g.101476991A>C , CM000665.1:g.101476991A>C	GRCh37
NC_000003.10:g.102959681A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1176A>C	ENSP00000419009.1:n.*1176A>C
ENST00000467655.2:c.*628A>C	ENSP00000418547.2:n.*628A>C
ENST00000704365.1:c.1541A>C	ENSP00000515873.1:p.Asp514Ala
ENST00000704366.1:c.1439A>C	ENSP00000515874.1:p.Asp480Ala
ENST00000704367.1:c.1262A>C	ENSP00000515875.1:p.Asp421Ala
ENST00000704368.1:n.2034A>C
ENST00000704369.1:c.1055A>C	ENSP00000515876.1:p.Asp352Ala
ENST00000704370.1:c.1535A>C	ENSP00000515877.1:p.Asp512Ala
ENST00000704372.1:n.1895A>C
ENST00000704444.1:c.1325A>C	ENSP00000515896.1:p.Asp442Ala
ENST00000704445.1:c.1193A>C	ENSP00000515897.1:p.Asp398Ala
ENST00000704446.1:c.1048+951A>C	ENSP00000515898.1:n.1048+951A>C
ENST00000341893.8:c.1541A>C MANE Select	ENSP00000342510.3:p.Asp514Ala
ENST00000341893.7:c.1541A>C	ENSP00000342510.3:p.Asp514Ala
ENST00000467655.1:c.1156A>C	ENSP00000418547.1:n.1156A>C
ENST00000489172.5:n.1523A>C
ENST00000494050.5:c.1364A>C	ENSP00000418185.1:p.Asp455Ala
NM_001303401.1:c.1364A>C	NP_001290330.1:p.Asp455Ala
NM_024548.3:c.1541A>C	NP_078824.2:p.Asp514Ala
XM_006713743.2:c.1439A>C	XP_006713806.1:p.Asp480Ala
XM_011513125.1:c.1325A>C	XP_011511427.1:p.Asp442Ala
XM_011513126.1:c.1325A>C	XP_011511428.1:p.Asp442Ala
XM_011513127.1:c.1193A>C	XP_011511429.1:p.Asp398Ala
XM_006713743.4:c.1439A>C	XP_006713806.1:p.Asp480Ala
XM_017007178.2:c.1262A>C	XP_016862667.1:p.Asp421Ala
NM_024548.4:c.1541A>C MANE Select	NP_078824.2:p.Asp514Ala
NM_001303401.2:c.1364A>C	NP_001290330.1:p.Asp455Ala