Canonical Allele Identifier: CA6239364
Gene: CEP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 539588
dbSNP Id: rs139110744

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.95799281C>T , CM000673.2:g.95799281C>T GRCh38
NC_000011.9:g.95532445C>T , CM000673.1:g.95532445C>T GRCh37
NC_000011.8:g.95172093C>T NCBI36
NG_029829.1:g.13821C>T , LRG_526:g.13821C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325542.10:c.95C>T MANE Select ENSP00000317902.5:p.Ser32Phe
ENST00000325486.9:c.95C>T ENSP00000317487.5:p.Ser32Phe
ENST00000325542.9:c.95C>T ENSP00000317902.5:p.Ser32Phe
ENST00000535497.1:c.45+8538C>T ENSP00000442481.1:n.45+8538C>T
ENST00000537677.5:c.14C>T ENSP00000441392.1:p.Ser5Phe
ENST00000538095.1:c.*75C>T ENSP00000443866.1:n.*75C>T
ENST00000538658.5:c.95C>T ENSP00000445706.1:p.Ser32Phe
ENST00000539855.5:c.95C>T ENSP00000437422.1:p.Ser32Phe
ENST00000540830.5:c.95C>T ENSP00000440996.1:p.Ser32Phe
ENST00000541150.5:c.68C>T ENSP00000443436.1:p.Ser23Phe
ENST00000541365.5:c.14C>T ENSP00000445821.1:p.Ser5Phe
ENST00000544522.5:c.68C>T ENSP00000438065.1:p.Ser23Phe
NM_001243776.1:c.68C>T NP_001230705.1:p.Ser23Phe
NM_001243777.1:c.95C>T NP_001230706.1:p.Ser32Phe
NM_014679.4:c.95C>T NP_055494.2:p.Ser32Phe
XM_006718945.2:c.95C>T XP_006719008.1:p.Ser32Phe
XM_006718946.2:c.95C>T XP_006719009.1:p.Ser32Phe
NM_001363604.1:c.14C>T NP_001350533.1:p.Ser5Phe
XM_006718945.3:c.95C>T XP_006719008.1:p.Ser32Phe
XM_006718946.3:c.95C>T XP_006719009.1:p.Ser32Phe
XM_017018592.1:c.68C>T XP_016874081.1:p.Ser23Phe
XM_017018593.2:c.95C>T XP_016874082.1:p.Ser32Phe
XM_017018594.2:c.95C>T XP_016874083.1:p.Ser32Phe
XM_024448779.1:c.14C>T XP_024304547.1:p.Ser5Phe
XR_001748050.2:n.323C>T
NM_014679.5:c.95C>T MANE Select NP_055494.2:p.Ser32Phe
NM_001243776.2:c.68C>T NP_001230705.1:p.Ser23Phe
NM_001243777.2:c.95C>T NP_001230706.1:p.Ser32Phe
NM_001363604.2:c.14C>T NP_001350533.1:p.Ser5Phe