Canonical Allele Identifier: CA1388867438

Gene: CEP97

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757833A= , CM000665.2:g.101757833A=	GRCh38
NC_000003.11:g.101476677A= , CM000665.1:g.101476677A=	GRCh37
NC_000003.10:g.102959367A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*862A=	ENSP00000419009.1:n.*862A=
ENST00000467655.2:c.*314A=	ENSP00000418547.2:n.*314A=
ENST00000704365.1:c.1227A=	ENSP00000515873.1:p.Ala409=
ENST00000704366.1:c.1125A=	ENSP00000515874.1:p.Ala375=
ENST00000704367.1:c.948A=	ENSP00000515875.1:p.Ala316=
ENST00000704368.1:n.1720A=
ENST00000704369.1:c.741A=	ENSP00000515876.1:p.Ala247=
ENST00000704370.1:c.1221A=	ENSP00000515877.1:p.Ala407=
ENST00000704372.1:n.1581A=
ENST00000704444.1:c.1011A=	ENSP00000515896.1:p.Ala337=
ENST00000704445.1:c.879A=	ENSP00000515897.1:p.Ala293=
ENST00000704446.1:c.1048+637A=	ENSP00000515898.1:n.1048+637A=
ENST00000341893.8:c.1227A= MANE Select	ENSP00000342510.3:p.Ala409=
ENST00000341893.7:c.1227A=	ENSP00000342510.3:p.Ala409=
ENST00000467655.1:c.842A=	ENSP00000418547.1:n.842A=
ENST00000489172.5:n.1209A=
ENST00000494050.5:c.1050A=	ENSP00000418185.1:p.Ala350=
NM_001303401.1:c.1050A=	NP_001290330.1:p.Ala350=
NM_024548.3:c.1227A=	NP_078824.2:p.Ala409=
XM_006713743.2:c.1125A=	XP_006713806.1:p.Ala375=
XM_011513125.1:c.1011A=	XP_011511427.1:p.Ala337=
XM_011513126.1:c.1011A=	XP_011511428.1:p.Ala337=
XM_011513127.1:c.879A=	XP_011511429.1:p.Ala293=
XM_006713743.4:c.1125A=	XP_006713806.1:p.Ala375=
XM_017007178.2:c.948A=	XP_016862667.1:p.Ala316=
NM_024548.4:c.1227A= MANE Select	NP_078824.2:p.Ala409=
NM_001303401.2:c.1050A=	NP_001290330.1:p.Ala350=