Canonical Allele Identifier: CA353877372

Gene: CEP97

Linked Data

• MyVariant Identifiers: chr3:g.101476795G>A (hg19) ; chr3:g.101757951G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101757951G>A , CM000665.2:g.101757951G>A	GRCh38
NC_000003.11:g.101476795G>A , CM000665.1:g.101476795G>A	GRCh37
NC_000003.10:g.102959485G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465011.2:c.*980G>A	ENSP00000419009.1:n.*980G>A
ENST00000467655.2:c.*432G>A	ENSP00000418547.2:n.*432G>A
ENST00000704365.1:c.1345G>A	ENSP00000515873.1:p.Asp449Asn
ENST00000704366.1:c.1243G>A	ENSP00000515874.1:p.Asp415Asn
ENST00000704367.1:c.1066G>A	ENSP00000515875.1:p.Asp356Asn
ENST00000704368.1:n.1838G>A
ENST00000704369.1:c.859G>A	ENSP00000515876.1:p.Asp287Asn
ENST00000704370.1:c.1339G>A	ENSP00000515877.1:p.Asp447Asn
ENST00000704372.1:n.1699G>A
ENST00000704444.1:c.1129G>A	ENSP00000515896.1:p.Asp377Asn
ENST00000704445.1:c.997G>A	ENSP00000515897.1:p.Asp333Asn
ENST00000704446.1:c.1048+755G>A	ENSP00000515898.1:n.1048+755G>A
ENST00000341893.8:c.1345G>A MANE Select	ENSP00000342510.3:p.Asp449Asn
ENST00000341893.7:c.1345G>A	ENSP00000342510.3:p.Asp449Asn
ENST00000467655.1:c.960G>A	ENSP00000418547.1:n.960G>A
ENST00000489172.5:n.1327G>A
ENST00000494050.5:c.1168G>A	ENSP00000418185.1:p.Asp390Asn
NM_001303401.1:c.1168G>A	NP_001290330.1:p.Asp390Asn
NM_024548.3:c.1345G>A	NP_078824.2:p.Asp449Asn
XM_006713743.2:c.1243G>A	XP_006713806.1:p.Asp415Asn
XM_011513125.1:c.1129G>A	XP_011511427.1:p.Asp377Asn
XM_011513126.1:c.1129G>A	XP_011511428.1:p.Asp377Asn
XM_011513127.1:c.997G>A	XP_011511429.1:p.Asp333Asn
XM_006713743.4:c.1243G>A	XP_006713806.1:p.Asp415Asn
XM_017007178.2:c.1066G>A	XP_016862667.1:p.Asp356Asn
NM_024548.4:c.1345G>A MANE Select	NP_078824.2:p.Asp449Asn
NM_001303401.2:c.1168G>A	NP_001290330.1:p.Asp390Asn