Canonical Allele Identifier: CA2804076584

Gene: CEP152

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48700641G>A , CM000677.2:g.48700641G>A	GRCh38
NC_000015.9:g.48992838G>A , CM000677.1:g.48992838G>A	GRCh37
NC_000015.8:g.46780130G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931770.1:n.5210+16377C>T
XR_931771.1:n.5210+16377C>T
XR_931772.1:n.5210+16377C>T
XR_931773.1:n.5210+16377C>T
XR_931775.1:n.5180+16377C>T
XR_001751153.2:n.5295+16377C>T
XR_931770.3:n.5196+16377C>T
XR_931775.3:n.5166+16377C>T