Canonical Allele Identifier: CA1388867458

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757875G= , CM000665.2:g.101757875G=	GRCh38
NC_000003.11:g.101476719G= , CM000665.1:g.101476719G=	GRCh37
NC_000003.10:g.102959409G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*904G=	ENSP00000419009.1:n.*904G=
ENST00000467655.2:c.*356G=	ENSP00000418547.2:n.*356G=
ENST00000704365.1:c.1269G=	ENSP00000515873.1:p.Leu423=
ENST00000704366.1:c.1167G=	ENSP00000515874.1:p.Leu389=
ENST00000704367.1:c.990G=	ENSP00000515875.1:p.Leu330=
ENST00000704368.1:n.1762G=
ENST00000704369.1:c.783G=	ENSP00000515876.1:p.Leu261=
ENST00000704370.1:c.1263G=	ENSP00000515877.1:p.Leu421=
ENST00000704372.1:n.1623G=
ENST00000704444.1:c.1053G=	ENSP00000515896.1:p.Leu351=
ENST00000704445.1:c.921G=	ENSP00000515897.1:p.Leu307=
ENST00000704446.1:c.1048+679G=	ENSP00000515898.1:n.1048+679G=
ENST00000341893.8:c.1269G= MANE Select	ENSP00000342510.3:p.Leu423=
ENST00000341893.7:c.1269G=	ENSP00000342510.3:p.Leu423=
ENST00000467655.1:c.884G=	ENSP00000418547.1:n.884G=
ENST00000489172.5:n.1251G=
ENST00000494050.5:c.1092G=	ENSP00000418185.1:p.Leu364=
NM_001303401.1:c.1092G=	NP_001290330.1:p.Leu364=
NM_024548.3:c.1269G=	NP_078824.2:p.Leu423=
XM_006713743.2:c.1167G=	XP_006713806.1:p.Leu389=
XM_011513125.1:c.1053G=	XP_011511427.1:p.Leu351=
XM_011513126.1:c.1053G=	XP_011511428.1:p.Leu351=
XM_011513127.1:c.921G=	XP_011511429.1:p.Leu307=
XM_006713743.4:c.1167G=	XP_006713806.1:p.Leu389=
XM_017007178.2:c.990G=	XP_016862667.1:p.Leu330=
NM_024548.4:c.1269G= MANE Select	NP_078824.2:p.Leu423=
NM_001303401.2:c.1092G=	NP_001290330.1:p.Leu364=