Canonical Allele Identifier: CA434872951

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476674T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757830T>C , CM000665.2:g.101757830T>C	GRCh38
NC_000003.11:g.101476674T>C , CM000665.1:g.101476674T>C	GRCh37
NC_000003.10:g.102959364T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*859T>C	ENSP00000419009.1:n.*859T>C
ENST00000467655.2:c.*311T>C	ENSP00000418547.2:n.*311T>C
ENST00000704365.1:c.1224T>C	ENSP00000515873.1:p.Val408=
ENST00000704366.1:c.1122T>C	ENSP00000515874.1:p.Val374=
ENST00000704367.1:c.945T>C	ENSP00000515875.1:p.Val315=
ENST00000704368.1:n.1717T>C
ENST00000704369.1:c.738T>C	ENSP00000515876.1:p.Val246=
ENST00000704370.1:c.1218T>C	ENSP00000515877.1:p.Val406=
ENST00000704372.1:n.1578T>C
ENST00000704444.1:c.1008T>C	ENSP00000515896.1:p.Val336=
ENST00000704445.1:c.876T>C	ENSP00000515897.1:p.Val292=
ENST00000704446.1:c.1048+634T>C	ENSP00000515898.1:n.1048+634T>C
ENST00000341893.8:c.1224T>C MANE Select	ENSP00000342510.3:p.Val408=
ENST00000341893.7:c.1224T>C	ENSP00000342510.3:p.Val408=
ENST00000467655.1:c.839T>C	ENSP00000418547.1:n.839T>C
ENST00000489172.5:n.1206T>C
ENST00000494050.5:c.1047T>C	ENSP00000418185.1:p.Val349=
NM_001303401.1:c.1047T>C	NP_001290330.1:p.Val349=
NM_024548.3:c.1224T>C	NP_078824.2:p.Val408=
XM_006713743.2:c.1122T>C	XP_006713806.1:p.Val374=
XM_011513125.1:c.1008T>C	XP_011511427.1:p.Val336=
XM_011513126.1:c.1008T>C	XP_011511428.1:p.Val336=
XM_011513127.1:c.876T>C	XP_011511429.1:p.Val292=
XM_006713743.4:c.1122T>C	XP_006713806.1:p.Val374=
XM_017007178.2:c.945T>C	XP_016862667.1:p.Val315=
NM_024548.4:c.1224T>C MANE Select	NP_078824.2:p.Val408=
NM_001303401.2:c.1047T>C	NP_001290330.1:p.Val349=