Canonical Allele Identifier: CA392343409

Gene: CEP152

Linked Data

• gnomAD v4: 15-48756454-G-C
• MyVariant Identifiers: chr15:g.49048651G>C (hg19) ; chr15:g.48756454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48756454G>C , CM000677.2:g.48756454G>C	GRCh38
NC_000015.9:g.49048651G>C , CM000677.1:g.49048651G>C	GRCh37
NC_000015.8:g.46835943G>C	NCBI36
NG_027518.1:g.59693C>G
NG_027518.2:g.59693C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380950.7:c.2794C>G MANE Select	ENSP00000370337.2:p.His932Asp
ENST00000325747.9:c.2515C>G	ENSP00000321000.5:p.His839Asp
ENST00000380950.6:c.2794C>G	ENSP00000370337.2:p.His932Asp
ENST00000399334.7:c.2794C>G	ENSP00000382271.3:p.His932Asp
NM_001194998.1:c.2794C>G	NP_001181927.1:p.His932Asp
NM_014985.3:c.2794C>G	NP_055800.2:p.His932Asp
XM_006720437.2:c.2794C>G	XP_006720500.1:p.His932Asp
XM_011521373.1:c.2794C>G	XP_011519675.1:p.His932Asp
XM_011521374.1:c.2794C>G	XP_011519676.1:p.His932Asp
XM_011521375.1:c.2794C>G	XP_011519677.1:p.His932Asp
XM_011521376.1:c.2794C>G	XP_011519678.1:p.His932Asp
XM_011521377.1:c.2794C>G	XP_011519679.1:p.His932Asp
XM_011521378.1:c.2794C>G	XP_011519680.1:p.His932Asp
XM_011521379.1:c.2794C>G	XP_011519681.1:p.His932Asp
XM_011521380.1:c.835C>G	XP_011519682.1:p.His279Asp
XM_011521381.1:c.829C>G	XP_011519683.1:p.His277Asp
XR_931769.1:n.3759C>G
XR_931770.1:n.3759C>G
XR_931771.1:n.3759C>G
XR_931772.1:n.3759C>G
XR_931773.1:n.3759C>G
XR_931774.1:n.3759C>G
XR_931775.1:n.3759C>G
XM_006720437.3:c.2794C>G	XP_006720500.1:p.His932Asp
XM_011521373.3:c.2794C>G	XP_011519675.1:p.His932Asp
XM_011521374.3:c.2794C>G	XP_011519676.1:p.His932Asp
XM_011521375.3:c.2794C>G	XP_011519677.1:p.His932Asp
XM_011521378.3:c.2794C>G	XP_011519680.1:p.His932Asp
XM_011521379.3:c.2794C>G	XP_011519681.1:p.His932Asp
XM_011521381.2:c.829C>G	XP_011519683.1:p.His277Asp
XM_017022015.1:c.829C>G	XP_016877504.1:p.His277Asp
XM_024449875.1:c.2794C>G	XP_024305643.1:p.His932Asp
XR_001751153.2:n.3745C>G
XR_931769.3:n.3745C>G
XR_931770.3:n.3745C>G
XR_931775.3:n.3745C>G
NM_001194998.2:c.2794C>G MANE Select	NP_001181927.1:p.His932Asp
NM_014985.4:c.2794C>G	NP_055800.2:p.His932Asp