Canonical Allele Identifier: CA7707399
Community Standard Title: NM_032856.5(WDR73):c.442G>A (p.Gly148Arg)
Gene: WDR73 HGNC NCBI
SCAND2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.84646259C>T , CM000677.2:g.84646259C>T GRCh38
NC_000015.9:g.85189490C>T , CM000677.1:g.85189490C>T GRCh37
NC_000015.8:g.82990494C>T NCBI36
NG_042034.1:g.13085G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032856.5:c.442G>A (WDR73) MANE Select NP_116245.2:p.Gly148Arg
ENST00000434634.7:c.442G>A (WDR73) MANE Select ENSP00000387982.3:p.Gly148Arg
NM_032856.3:c.442G>A (WDR73) NP_116245.2:p.Gly148Arg
NR_130944.1:n.948G>A (WDR73)
NR_130944.2:n.985G>A (WDR73)
NR_130945.1:n.511G>A (WDR73)
NR_130945.2:n.451G>A (WDR73)
NR_130946.1:n.518G>A (WDR73)
NR_130946.2:n.458G>A (WDR73)
NR_130947.1:n.422G>A (WDR73)
NR_130947.2:n.362G>A (WDR73)
ENST00000348993.9:n.7756C>T (SCAND2P)
ENST00000398528.7:n.518G>A (WDR73)
ENST00000434634.6:c.442G>A (WDR73) ENSP00000387982.2:p.Gly148Arg
ENST00000558521.5:c.441G>A (WDR73)
ENST00000558608.1:n.787G>A (WDR73)
ENST00000559015.5:n.1030G>A (WDR73)
ENST00000559126.5:n.948G>A (WDR73)
ENST00000559178.5:c.760G>A (WDR73)
ENST00000559224.5:c.345G>A (WDR73)
ENST00000559452.5:n.906G>A (WDR73)
ENST00000559994.5:n.455G>A (WDR73)
ENST00000560088.5:n.452G>A (WDR73)
ENST00000560835.5:n.458G>A (WDR73)
ENST00000560966.5:n.3767G>A (WDR73)
ENST00000561329.5:n.442G>A (WDR73)
XR_001751407.2:n.451G>A (WDR73)
XR_001751408.2:n.458G>A (WDR73)
XR_243214.1:n.458G>A (WDR73)
XR_243214.3:n.458G>A (WDR73)