Canonical Allele Identifier: CA1388867368

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757675_101757678delinsAATG , CM000665.2:g.101757675_101757678delinsAATG	GRCh38
NC_000003.11:g.101476519_101476522delinsAATG , CM000665.1:g.101476519_101476522delinsAATG	GRCh37
NC_000003.10:g.102959209_102959212delinsAATG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000465011.2:c.*704_*707delinsAATG	ENSP00000419009.1:n.*704_*707delinsAATG
ENST00000467655.2:c.*156_*159delinsAATG	ENSP00000418547.2:n.*156_*159delinsAATG
ENST00000704365.1:c.1069_1072delinsAATG	ENSP00000515873.1:p.Asn357=
ENST00000704366.1:c.967_970delinsAATG	ENSP00000515874.1:p.Asn323=
ENST00000704367.1:c.926-136_926-133delinsAATG	ENSP00000515875.1:n.926-136_926-133delinsAATG
ENST00000704368.1:n.1562_1565delinsAATG
ENST00000704369.1:c.583_586delinsAATG	ENSP00000515876.1:p.Asn195=
ENST00000704370.1:c.1063_1066delinsAATG	ENSP00000515877.1:p.Asn355=
ENST00000704372.1:n.1423_1426delinsAATG
ENST00000704444.1:c.853_856delinsAATG	ENSP00000515896.1:p.Asn285=
ENST00000704445.1:c.721_724delinsAATG	ENSP00000515897.1:p.Asn241=
ENST00000704446.1:c.1048+479_1048+482delinsAATG	ENSP00000515898.1:n.1048+479_1048+482delinsAATG
ENST00000341893.8:c.1069_1072delinsAATG MANE Select	ENSP00000342510.3:p.Asn357=
ENST00000341893.7:c.1069_1072delinsAATG	ENSP00000342510.3:p.Asn357=
ENST00000467655.1:c.684_687delinsAATG	ENSP00000418547.1:n.684_687delinsAATG
ENST00000489172.5:n.1051_1054delinsAATG
ENST00000494050.5:c.1028-136_1028-133delinsAATG	ENSP00000418185.1:n.1028-136_1028-133delinsAATG
NM_001303401.1:c.1028-136_1028-133delinsAATG	NP_001290330.1:n.1028-136_1028-133delinsAATG
NM_024548.3:c.1069_1072delinsAATG	NP_078824.2:p.Asn357=
XM_006713743.2:c.967_970delinsAATG	XP_006713806.1:p.Asn323=
XM_011513125.1:c.853_856delinsAATG	XP_011511427.1:p.Asn285=
XM_011513126.1:c.853_856delinsAATG	XP_011511428.1:p.Asn285=
XM_011513127.1:c.721_724delinsAATG	XP_011511429.1:p.Asn241=
XM_006713743.4:c.967_970delinsAATG	XP_006713806.1:p.Asn323=
XM_017007178.2:c.926-136_926-133delinsAATG	XP_016862667.1:n.926-136_926-133delinsAATG
NM_024548.4:c.1069_1072delinsAATG MANE Select	NP_078824.2:p.Asn357=
NM_001303401.2:c.1028-136_1028-133delinsAATG	NP_001290330.1:n.1028-136_1028-133delinsAATG