Canonical Allele Identifier: CA7707546
Community Standard Title: NM_032856.5(WDR73):c.21G>A (p.Trp7Ter)
Gene: WDR73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.84654254C>T , CM000677.2:g.84654254C>T GRCh38
NC_000015.9:g.85197485C>T , CM000677.1:g.85197485C>T GRCh37
NC_000015.8:g.82998489C>T NCBI36
NG_042034.1:g.5090G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032856.5:c.21G>A MANE Select NP_116245.2:p.Trp7Ter
ENST00000434634.7:c.21G>A MANE Select ENSP00000387982.3:p.Trp7Ter
NM_032856.3:c.21G>A NP_116245.2:p.Trp7Ter
NR_130944.2:n.30G>A
NR_130945.1:n.90G>A
NR_130945.2:n.30G>A
NR_130946.1:n.90G>A
NR_130946.2:n.30G>A
NR_130947.1:n.90G>A
NR_130947.2:n.30G>A
ENST00000398528.7:n.90G>A
ENST00000434634.6:c.21G>A ENSP00000387982.2:p.Trp7Ter
ENST00000558019.5:n.30G>A
ENST00000558521.5:c.20G>A
ENST00000559015.5:n.27G>A
ENST00000559178.5:c.5G>A
ENST00000559224.5:c.13G>A
ENST00000559452.5:n.19G>A
ENST00000559994.5:n.27G>A
ENST00000560252.5:n.45G>A
ENST00000560835.5:n.30G>A
ENST00000561329.5:n.21G>A
ENST00000561434.1:n.37G>A
XR_001751407.2:n.30G>A
XR_001751408.2:n.37G>A
XR_243214.1:n.37G>A
XR_243214.3:n.37G>A