Canonical Allele Identifier: CA9359298

Gene: CEP89

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32915471G>A , CM000681.2:g.32915471G>A	GRCh38
NC_000019.9:g.33406377G>A , CM000681.1:g.33406377G>A	GRCh37
NC_000019.8:g.38098217G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305768.10:c.1431C>T MANE Select	ENSP00000306105.4:p.His477=
ENST00000305768.9:c.1431C>T	ENSP00000306105.4:p.His477=
ENST00000586984.6:c.*40C>T	ENSP00000465141.1:n.*40C>T
ENST00000591698.5:c.1287C>T	ENSP00000467544.1:n.1287C>T
NM_032816.4:c.1431C>T	NP_116205.3:p.His477=
XM_005259344.2:c.1359C>T	XP_005259401.1:p.His453=
XM_005259346.2:c.*35C>T	XP_005259403.1:n.*35C>T
XM_011527425.1:c.690C>T	XP_011525727.1:p.His230=
XR_935866.1:n.1477C>T
XM_005259344.3:c.1359C>T	XP_005259401.1:p.His453=
XM_017027398.1:c.1431C>T	XP_016882887.1:p.His477=
XM_024451745.1:c.690C>T	XP_024307513.1:p.His230=
XR_002958372.1:n.1613C>T
XR_935866.2:n.1477C>T
NM_032816.5:c.1431C>T MANE Select	NP_116205.3:p.His477=