Canonical Allele Identifier: CA1388867293
Gene: CEP97 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101757483_101757488delinsTGTTTG , CM000665.2:g.101757483_101757488delinsTGTTTG GRCh38
NC_000003.11:g.101476327_101476332delinsTGTTTG , CM000665.1:g.101476327_101476332delinsTGTTTG GRCh37
NC_000003.10:g.102959017_102959022delinsTGTTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*663-151_*663-146delinsTGTTTG ENSP00000419009.1:n.*663-151_*663-146delinsTGTTTG
ENST00000467655.2:c.*115-151_*115-146delinsTGTTTG ENSP00000418547.2:n.*115-151_*115-146delinsTGTTTG
ENST00000704365.1:c.1028-151_1028-146delinsTGTTTG ENSP00000515873.1:n.1028-151_1028-146delinsTGTTTG
ENST00000704366.1:c.926-151_926-146delinsTGTTTG ENSP00000515874.1:n.926-151_926-146delinsTGTTTG
ENST00000704367.1:c.925+287_925+292delinsTGTTTG ENSP00000515875.1:n.925+287_925+292delinsTGTTTG
ENST00000704368.1:n.1370_1375delinsTGTTTG
ENST00000704369.1:c.542-151_542-146delinsTGTTTG ENSP00000515876.1:n.542-151_542-146delinsTGTTTG
ENST00000704370.1:c.1022-151_1022-146delinsTGTTTG ENSP00000515877.1:n.1022-151_1022-146delinsTGTTTG
ENST00000704372.1:n.1382-151_1382-146delinsTGTTTG
ENST00000704444.1:c.812-151_812-146delinsTGTTTG ENSP00000515896.1:n.812-151_812-146delinsTGTTTG
ENST00000704445.1:c.680-151_680-146delinsTGTTTG ENSP00000515897.1:n.680-151_680-146delinsTGTTTG
ENST00000704446.1:c.1048+287_1048+292delinsTGTTTG ENSP00000515898.1:n.1048+287_1048+292delinsTGTTTG
ENST00000341893.8:c.1028-151_1028-146delinsTGTTTG MANE Select ENSP00000342510.3:n.1028-151_1028-146delinsTGTTTG
ENST00000341893.7:c.1028-151_1028-146delinsTGTTTG ENSP00000342510.3:n.1028-151_1028-146delinsTGTTTG
ENST00000467655.1:c.643-151_643-146delinsTGTTTG ENSP00000418547.1:n.643-151_643-146delinsTGTTTG
ENST00000489172.5:n.1010-151_1010-146delinsTGTTTG
ENST00000494050.5:c.1027+287_1027+292delinsTGTTTG ENSP00000418185.1:n.1027+287_1027+292delinsTGTTTG
NM_001303401.1:c.1027+287_1027+292delinsTGTTTG NP_001290330.1:n.1027+287_1027+292delinsTGTTTG
NM_024548.3:c.1028-151_1028-146delinsTGTTTG NP_078824.2:n.1028-151_1028-146delinsTGTTTG
XM_006713743.2:c.926-151_926-146delinsTGTTTG XP_006713806.1:n.926-151_926-146delinsTGTTTG
XM_011513125.1:c.812-151_812-146delinsTGTTTG XP_011511427.1:n.812-151_812-146delinsTGTTTG
XM_011513126.1:c.812-151_812-146delinsTGTTTG XP_011511428.1:n.812-151_812-146delinsTGTTTG
XM_011513127.1:c.680-151_680-146delinsTGTTTG XP_011511429.1:n.680-151_680-146delinsTGTTTG
XM_006713743.4:c.926-151_926-146delinsTGTTTG XP_006713806.1:n.926-151_926-146delinsTGTTTG
XM_017007178.2:c.925+287_925+292delinsTGTTTG XP_016862667.1:n.925+287_925+292delinsTGTTTG
NM_024548.4:c.1028-151_1028-146delinsTGTTTG MANE Select NP_078824.2:n.1028-151_1028-146delinsTGTTTG
NM_001303401.2:c.1027+287_1027+292delinsTGTTTG NP_001290330.1:n.1027+287_1027+292delinsTGTTTG