Canonical Allele Identifier: CA382421084
Gene: CEP57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.95813094A>C , CM000673.2:g.95813094A>C GRCh38
NC_000011.9:g.95546258A>C , CM000673.1:g.95546258A>C GRCh37
NC_000011.8:g.95185906A>C NCBI36
NG_029829.1:g.27634A>C , LRG_526:g.27634A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325542.10:c.365A>C MANE Select ENSP00000317902.5:p.Glu122Ala
ENST00000325486.9:c.365A>C ENSP00000317487.5:p.Glu122Ala
ENST00000325542.9:c.365A>C ENSP00000317902.5:p.Glu122Ala
ENST00000535497.1:c.*82A>C ENSP00000442481.1:n.*82A>C
ENST00000536587.5:n.165A>C
ENST00000537677.5:c.284A>C ENSP00000441392.1:p.Glu95Ala
ENST00000538658.5:c.365A>C ENSP00000445706.1:p.Glu122Ala
ENST00000539855.5:c.*144A>C ENSP00000437422.1:n.*144A>C
ENST00000540830.5:c.*129A>C ENSP00000440996.1:n.*129A>C
ENST00000541150.5:c.338A>C ENSP00000443436.1:p.Glu113Ala
ENST00000541365.5:c.284A>C ENSP00000445821.1:p.Glu95Ala
ENST00000541768.1:n.118A>C
ENST00000544522.5:c.338A>C ENSP00000438065.1:p.Glu113Ala
NM_001243776.1:c.338A>C NP_001230705.1:p.Glu113Ala
NM_001243777.1:c.365A>C NP_001230706.1:p.Glu122Ala
NM_014679.4:c.365A>C NP_055494.2:p.Glu122Ala
XM_006718945.2:c.365A>C XP_006719008.1:p.Glu122Ala
XM_006718946.2:c.365A>C XP_006719009.1:p.Glu122Ala
NM_001363604.1:c.284A>C NP_001350533.1:p.Glu95Ala
XM_006718945.3:c.365A>C XP_006719008.1:p.Glu122Ala
XM_006718946.3:c.365A>C XP_006719009.1:p.Glu122Ala
XM_017018592.1:c.338A>C XP_016874081.1:p.Glu113Ala
XM_017018593.2:c.365A>C XP_016874082.1:p.Glu122Ala
XM_017018594.2:c.365A>C XP_016874083.1:p.Glu122Ala
XM_024448779.1:c.284A>C XP_024304547.1:p.Glu95Ala
XR_001748050.2:n.593A>C
NM_014679.5:c.365A>C MANE Select NP_055494.2:p.Glu122Ala
NM_001243776.2:c.338A>C NP_001230705.1:p.Glu113Ala
NM_001243777.2:c.365A>C NP_001230706.1:p.Glu122Ala
NM_001363604.2:c.284A>C NP_001350533.1:p.Glu95Ala