Canonical Allele Identifier: CA2175628958

Gene: CEP152

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48756265C= , CM000677.2:g.48756265C=	GRCh38
NC_000015.9:g.49048462C= , CM000677.1:g.49048462C=	GRCh37
NC_000015.8:g.46835754C=	NCBI36
NG_027518.1:g.59882G=
NG_027518.2:g.59882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380950.7:c.2983G= MANE Select	ENSP00000370337.2:p.Ala995=
ENST00000325747.9:c.2704G=	ENSP00000321000.5:p.Ala902=
ENST00000380950.6:c.2983G=	ENSP00000370337.2:p.Ala995=
ENST00000399334.7:c.2983G=	ENSP00000382271.3:p.Ala995=
NM_001194998.1:c.2983G=	NP_001181927.1:p.Ala995=
NM_014985.3:c.2983G=	NP_055800.2:p.Ala995=
XM_006720437.2:c.2983G=	XP_006720500.1:p.Ala995=
XM_011521373.1:c.2983G=	XP_011519675.1:p.Ala995=
XM_011521374.1:c.2983G=	XP_011519676.1:p.Ala995=
XM_011521375.1:c.2983G=	XP_011519677.1:p.Ala995=
XM_011521376.1:c.2983G=	XP_011519678.1:p.Ala995=
XM_011521377.1:c.2983G=	XP_011519679.1:p.Ala995=
XM_011521378.1:c.2983G=	XP_011519680.1:p.Ala995=
XM_011521379.1:c.2983G=	XP_011519681.1:p.Ala995=
XM_011521380.1:c.1024G=	XP_011519682.1:p.Ala342=
XM_011521381.1:c.1018G=	XP_011519683.1:p.Ala340=
XR_931769.1:n.3948G=
XR_931770.1:n.3948G=
XR_931771.1:n.3948G=
XR_931772.1:n.3948G=
XR_931773.1:n.3948G=
XR_931774.1:n.3948G=
XR_931775.1:n.3948G=
XM_006720437.3:c.2983G=	XP_006720500.1:p.Ala995=
XM_011521373.3:c.2983G=	XP_011519675.1:p.Ala995=
XM_011521374.3:c.2983G=	XP_011519676.1:p.Ala995=
XM_011521375.3:c.2983G=	XP_011519677.1:p.Ala995=
XM_011521378.3:c.2983G=	XP_011519680.1:p.Ala995=
XM_011521379.3:c.2983G=	XP_011519681.1:p.Ala995=
XM_011521381.2:c.1018G=	XP_011519683.1:p.Ala340=
XM_017022015.1:c.1018G=	XP_016877504.1:p.Ala340=
XM_024449875.1:c.2983G=	XP_024305643.1:p.Ala995=
XR_001751153.2:n.3934G=
XR_931769.3:n.3934G=
XR_931770.3:n.3934G=
XR_931775.3:n.3934G=
NM_001194998.2:c.2983G= MANE Select	NP_001181927.1:p.Ala995=
NM_014985.4:c.2983G=	NP_055800.2:p.Ala995=