Canonical Allele Identifier: CA1388867501

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101758007G= , CM000665.2:g.101758007G=	GRCh38
NC_000003.11:g.101476851G= , CM000665.1:g.101476851G=	GRCh37
NC_000003.10:g.102959541G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*1036G=	ENSP00000419009.1:n.*1036G=
ENST00000467655.2:c.*488G=	ENSP00000418547.2:n.*488G=
ENST00000704365.1:c.1401G=	ENSP00000515873.1:p.Met467=
ENST00000704366.1:c.1299G=	ENSP00000515874.1:p.Met433=
ENST00000704367.1:c.1122G=	ENSP00000515875.1:p.Met374=
ENST00000704368.1:n.1894G=
ENST00000704369.1:c.915G=	ENSP00000515876.1:p.Met305=
ENST00000704370.1:c.1395G=	ENSP00000515877.1:p.Met465=
ENST00000704372.1:n.1755G=
ENST00000704444.1:c.1185G=	ENSP00000515896.1:p.Met395=
ENST00000704445.1:c.1053G=	ENSP00000515897.1:p.Met351=
ENST00000704446.1:c.1048+811G=	ENSP00000515898.1:n.1048+811G=
ENST00000341893.8:c.1401G= MANE Select	ENSP00000342510.3:p.Met467=
ENST00000341893.7:c.1401G=	ENSP00000342510.3:p.Met467=
ENST00000467655.1:c.1016G=	ENSP00000418547.1:n.1016G=
ENST00000489172.5:n.1383G=
ENST00000494050.5:c.1224G=	ENSP00000418185.1:p.Met408=
NM_001303401.1:c.1224G=	NP_001290330.1:p.Met408=
NM_024548.3:c.1401G=	NP_078824.2:p.Met467=
XM_006713743.2:c.1299G=	XP_006713806.1:p.Met433=
XM_011513125.1:c.1185G=	XP_011511427.1:p.Met395=
XM_011513126.1:c.1185G=	XP_011511428.1:p.Met395=
XM_011513127.1:c.1053G=	XP_011511429.1:p.Met351=
XM_006713743.4:c.1299G=	XP_006713806.1:p.Met433=
XM_017007178.2:c.1122G=	XP_016862667.1:p.Met374=
NM_024548.4:c.1401G= MANE Select	NP_078824.2:p.Met467=
NM_001303401.2:c.1224G=	NP_001290330.1:p.Met408=