Canonical Allele Identifier: CA5608869

Gene: CEP55

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93503223C>T , CM000672.2:g.93503223C>T	GRCh38
NC_000010.10:g.95262980C>T , CM000672.1:g.95262980C>T	GRCh37
NC_000010.9:g.95252970C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371485.8:c.294C>T MANE Select	ENSP00000360540.3:p.Thr98=
ENST00000371485.7:c.294C>T	ENSP00000360540.3:p.Thr98=
NM_001127182.1:c.294C>T	NP_001120654.1:p.Thr98=
NM_018131.4:c.294C>T	NP_060601.3:p.Thr98=
XM_011539918.1:c.-214C>T	XP_011538220.1:n.-214C>T
XM_011539919.1:c.-214C>T	XP_011538221.1:n.-214C>T
XM_011539920.1:c.-214C>T	XP_011538222.1:n.-214C>T
XM_011539920.2:c.-214C>T	XP_011538222.1:n.-214C>T
XM_017016372.1:c.-214C>T	XP_016871861.1:n.-214C>T
XM_017016373.1:c.-214C>T	XP_016871862.1:n.-214C>T
NM_001127182.2:c.294C>T	NP_001120654.2:p.Thr98=
NM_018131.5:c.294C>T MANE Select	NP_060601.4:p.Thr98=