Canonical Allele Identifier: CA1388867366
Gene: CEP97 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101757662_101757663delinsTG , CM000665.2:g.101757662_101757663delinsTG GRCh38
NC_000003.11:g.101476506_101476507delinsTG , CM000665.1:g.101476506_101476507delinsTG GRCh37
NC_000003.10:g.102959196_102959197delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465011.2:c.*691_*692delinsTG ENSP00000419009.1:n.*691_*692delinsTG
ENST00000467655.2:c.*143_*144delinsTG ENSP00000418547.2:n.*143_*144delinsTG
ENST00000704365.1:c.1056_1057delinsTG ENSP00000515873.1:p.Val352=
ENST00000704366.1:c.954_955delinsTG ENSP00000515874.1:p.Val318=
ENST00000704367.1:c.926-149_926-148delinsTG ENSP00000515875.1:n.926-149_926-148delinsTG
ENST00000704368.1:n.1549_1550delinsTG
ENST00000704369.1:c.570_571delinsTG ENSP00000515876.1:p.Val190=
ENST00000704370.1:c.1050_1051delinsTG ENSP00000515877.1:p.Val350=
ENST00000704372.1:n.1410_1411delinsTG
ENST00000704444.1:c.840_841delinsTG ENSP00000515896.1:p.Val280=
ENST00000704445.1:c.708_709delinsTG ENSP00000515897.1:p.Val236=
ENST00000704446.1:c.1048+466_1048+467delinsTG ENSP00000515898.1:n.1048+466_1048+467delinsTG
ENST00000341893.8:c.1056_1057delinsTG MANE Select ENSP00000342510.3:p.Val352=
ENST00000341893.7:c.1056_1057delinsTG ENSP00000342510.3:p.Val352=
ENST00000467655.1:c.671_672delinsTG ENSP00000418547.1:n.671_672delinsTG
ENST00000489172.5:n.1038_1039delinsTG
ENST00000494050.5:c.1028-149_1028-148delinsTG ENSP00000418185.1:n.1028-149_1028-148delinsTG
NM_001303401.1:c.1028-149_1028-148delinsTG NP_001290330.1:n.1028-149_1028-148delinsTG
NM_024548.3:c.1056_1057delinsTG NP_078824.2:p.Val352=
XM_006713743.2:c.954_955delinsTG XP_006713806.1:p.Val318=
XM_011513125.1:c.840_841delinsTG XP_011511427.1:p.Val280=
XM_011513126.1:c.840_841delinsTG XP_011511428.1:p.Val280=
XM_011513127.1:c.708_709delinsTG XP_011511429.1:p.Val236=
XM_006713743.4:c.954_955delinsTG XP_006713806.1:p.Val318=
XM_017007178.2:c.926-149_926-148delinsTG XP_016862667.1:n.926-149_926-148delinsTG
NM_024548.4:c.1056_1057delinsTG MANE Select NP_078824.2:p.Val352=
NM_001303401.2:c.1028-149_1028-148delinsTG NP_001290330.1:n.1028-149_1028-148delinsTG