Canonical Allele Identifier: CA3111609303

Gene: CEP135

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55965785C= , CM000666.2:g.55965785C=	GRCh38
NC_000004.11:g.56831951C= , CM000666.1:g.56831951C=	GRCh37
NC_000004.10:g.56526708C=	NCBI36
NG_032806.1:g.21978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257287.5:c.970C= MANE Select	ENSP00000257287.3:p.Gln324=
ENST00000257287.4:c.970C=	ENSP00000257287.3:p.Gln324=
ENST00000506202.1:n.920C=
ENST00000515081.1:n.604C=
NM_025009.4:c.970C=	NP_079285.2:p.Gln324=
XM_005265788.2:c.-98C=	XP_005265845.1:n.-98C=
XM_006714055.2:c.970C=	XP_006714118.1:p.Gln324=
XR_941063.1:n.472-782G=
XR_941064.1:n.471+4988G=
XM_005265788.4:c.-98C=	XP_005265845.1:n.-98C=
XM_006714055.3:c.970C=	XP_006714118.1:p.Gln324=
NM_025009.5:c.970C= MANE Select	NP_079285.2:p.Gln324=