Canonical Allele Identifier: CA7707182

Gene: WDR73 SCAND2P

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84643655G>A , CM000677.2:g.84643655G>A	GRCh38
NC_000015.9:g.85186886G>A , CM000677.1:g.85186886G>A	GRCh37
NC_000015.8:g.82987890G>A	NCBI36
NG_042034.1:g.15689C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032856.5:c.952C>T (WDR73) MANE Select	NP_116245.2:p.Arg318Trp
ENST00000434634.7:c.952C>T (WDR73) MANE Select	ENSP00000387982.3:p.Arg318Trp
NM_032856.3:c.952C>T (WDR73)	NP_116245.2:p.Arg318Trp
NR_130944.1:n.1458C>T (WDR73)
NR_130944.2:n.1495C>T (WDR73)
NR_130945.1:n.1134C>T (WDR73)
NR_130945.2:n.1074C>T (WDR73)
NR_130946.1:n.1028C>T (WDR73)
NR_130946.2:n.968C>T (WDR73)
NR_130947.1:n.932C>T (WDR73)
NR_130947.2:n.872C>T (WDR73)
ENST00000348993.9:n.5152G>A (SCAND2P)
ENST00000398528.7:n.1028C>T (WDR73)
ENST00000434634.6:c.952C>T (WDR73)	ENSP00000387982.2:p.Arg318Trp
ENST00000558608.1:n.1644C>T (WDR73)
ENST00000559015.5:n.1540C>T (WDR73)
ENST00000559126.5:n.1458C>T (WDR73)
ENST00000559994.5:n.1176C>T (WDR73)
XR_001751407.2:n.1197C>T (WDR73)
XR_001751408.2:n.1217C>T (WDR73)
XR_243214.1:n.1179C>T (WDR73)
XR_243214.3:n.1179C>T (WDR73)