Canonical Allele Identifier: CA382420269

Gene: CEP57

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.95812992T>C , CM000673.2:g.95812992T>C	GRCh38
NC_000011.9:g.95546156T>C , CM000673.1:g.95546156T>C	GRCh37
NC_000011.8:g.95185804T>C	NCBI36
NG_029829.1:g.27532T>C , LRG_526:g.27532T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325542.10:c.263T>C MANE Select	ENSP00000317902.5:p.Ile88Thr
ENST00000325486.9:c.263T>C	ENSP00000317487.5:p.Ile88Thr
ENST00000325542.9:c.263T>C	ENSP00000317902.5:p.Ile88Thr
ENST00000535497.1:c.106T>C	ENSP00000442481.1:p.Phe36Leu
ENST00000536587.5:n.63T>C
ENST00000537677.5:c.182T>C	ENSP00000441392.1:p.Ile61Thr
ENST00000538658.5:c.263T>C	ENSP00000445706.1:p.Ile88Thr
ENST00000539855.5:c.*42T>C	ENSP00000437422.1:n.*42T>C
ENST00000540830.5:c.*27T>C	ENSP00000440996.1:n.*27T>C
ENST00000541150.5:c.236T>C	ENSP00000443436.1:p.Ile79Thr
ENST00000541365.5:c.182T>C	ENSP00000445821.1:p.Ile61Thr
ENST00000541768.1:n.16T>C
ENST00000544522.5:c.236T>C	ENSP00000438065.1:p.Ile79Thr
NM_001243776.1:c.236T>C	NP_001230705.1:p.Ile79Thr
NM_001243777.1:c.263T>C	NP_001230706.1:p.Ile88Thr
NM_014679.4:c.263T>C	NP_055494.2:p.Ile88Thr
XM_006718945.2:c.263T>C	XP_006719008.1:p.Ile88Thr
XM_006718946.2:c.263T>C	XP_006719009.1:p.Ile88Thr
NM_001363604.1:c.182T>C	NP_001350533.1:p.Ile61Thr
XM_006718945.3:c.263T>C	XP_006719008.1:p.Ile88Thr
XM_006718946.3:c.263T>C	XP_006719009.1:p.Ile88Thr
XM_017018592.1:c.236T>C	XP_016874081.1:p.Ile79Thr
XM_017018593.2:c.263T>C	XP_016874082.1:p.Ile88Thr
XM_017018594.2:c.263T>C	XP_016874083.1:p.Ile88Thr
XM_024448779.1:c.182T>C	XP_024304547.1:p.Ile61Thr
XR_001748050.2:n.491T>C
NM_014679.5:c.263T>C MANE Select	NP_055494.2:p.Ile88Thr
NM_001243776.2:c.236T>C	NP_001230705.1:p.Ile79Thr
NM_001243777.2:c.263T>C	NP_001230706.1:p.Ile88Thr
NM_001363604.2:c.182T>C	NP_001350533.1:p.Ile61Thr