Canonical Allele Identifier: CA2573145847

Gene: CEP55

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93503223_93503224delinsTG , CM000672.2:g.93503223_93503224delinsTG	GRCh38
NC_000010.10:g.95262980_95262981delinsTG , CM000672.1:g.95262980_95262981delinsTG	GRCh37
NC_000010.9:g.95252970_95252971delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018131.5:c.294_295delinsTG MANE Select	NP_060601.4:p.Thr99Ala
ENST00000371485.8:c.294_295delinsTG MANE Select	ENSP00000360540.3:p.Thr99Ala
NM_001127182.2:c.294_295delinsTG	NP_001120654.2:p.Thr99Ala
ENST00000371485.7:c.294_295delinsTG	ENSP00000360540.3:p.Thr99Ala
XM_011539918.1:c.-214_-213delinsTG	XP_011538220.1:n.-214_-213delinsTG
XM_011539919.1:c.-214_-213delinsTG	XP_011538221.1:n.-214_-213delinsTG
XM_011539920.1:c.-214_-213delinsTG	XP_011538222.1:n.-214_-213delinsTG
XM_011539920.2:c.-214_-213delinsTG	XP_011538222.1:n.-214_-213delinsTG
XM_017016372.1:c.-214_-213delinsTG	XP_016871861.1:n.-214_-213delinsTG
XM_017016373.1:c.-214_-213delinsTG	XP_016871862.1:n.-214_-213delinsTG