Canonical Allele Identifier: CA2361682031

Gene: CEP250

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35509528C= , CM000682.2:g.35509528C=	GRCh38
NC_000020.10:g.34097357C= , CM000682.1:g.34097357C=	GRCh37
NC_000020.9:g.33560771C=	NCBI36
NG_051604.1:g.59391C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706827.1:c.*4804-470C=	ENSP00000516575.1:n.*4804-470C=
ENST00000706828.1:c.7180-470C=	ENSP00000516576.1:n.7180-470C=
ENST00000706829.1:c.7009-470C=	ENSP00000516577.1:n.7009-470C=
ENST00000706830.1:c.6895-470C=	ENSP00000516578.1:n.6895-470C=
ENST00000706831.1:n.4416-470C=
ENST00000706832.1:n.1569C=
ENST00000397527.6:c.7009-470C= MANE Select	ENSP00000380661.1:n.7009-470C=
ENST00000397527.5:c.7009-470C=	ENSP00000380661.1:n.7009-470C=
ENST00000422671.1:c.2370+1338C=	ENSP00000395992.1:n.2370+1338C=
NM_007186.4:c.7009-470C=	NP_009117.2:n.7009-470C=
XM_005260262.3:c.7009-470C=	XP_005260319.1:n.7009-470C=
XM_005260263.3:c.7009-470C=	XP_005260320.1:n.7009-470C=
XM_005260264.3:c.6778-470C=	XP_005260321.1:n.6778-470C=
XM_005260265.2:c.5113-470C=	XP_005260322.1:n.5113-470C=
XM_006723690.2:c.7009-470C=	XP_006723753.1:n.7009-470C=
XM_006723691.1:c.7009-470C=	XP_006723754.1:n.7009-470C=
XM_006723692.2:c.7009-470C=	XP_006723755.1:n.7009-470C=
XM_006723693.2:c.7009-470C=	XP_006723756.1:n.7009-470C=
XM_006723694.2:c.6895-470C=	XP_006723757.1:n.6895-470C=
XM_006723695.2:c.6841-470C=	XP_006723758.1:n.6841-470C=
XM_011528517.1:c.7009-470C=	XP_011526819.1:n.7009-470C=
XM_011528518.1:c.6640-470C=	XP_011526820.1:n.6640-470C=
XM_011528519.1:c.6403-470C=	XP_011526821.1:n.6403-470C=
NM_001318219.1:c.5113-470C=	NP_001305148.1:n.5113-470C=
NM_007186.5:c.7009-470C=	NP_009117.2:n.7009-470C=
XM_005260262.4:c.7009-470C=	XP_005260319.1:n.7009-470C=
XM_005260263.4:c.7009-470C=	XP_005260320.1:n.7009-470C=
XM_005260264.4:c.6778-470C=	XP_005260321.1:n.6778-470C=
XM_006723690.4:c.7009-470C=	XP_006723753.1:n.7009-470C=
XM_006723692.4:c.7009-470C=	XP_006723755.1:n.7009-470C=
XM_006723693.4:c.7009-470C=	XP_006723756.1:n.7009-470C=
XM_006723694.3:c.6895-470C=	XP_006723757.1:n.6895-470C=
XM_011528517.2:c.7009-470C=	XP_011526819.1:n.7009-470C=
XM_011528518.3:c.6640-470C=	XP_011526820.1:n.6640-470C=
XM_011528519.2:c.6403-470C=	XP_011526821.1:n.6403-470C=
XM_017027617.1:c.6895-470C=	XP_016883106.1:n.6895-470C=
XM_017027618.1:c.6277-470C=	XP_016883107.1:n.6277-470C=
XM_017027619.1:c.5611-470C=	XP_016883108.1:n.5611-470C=
NM_007186.6:c.7009-470C= MANE Select	NP_009117.2:n.7009-470C=