Canonical Allele Identifier: CA7707528

Gene: WDR73

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84654233C>G , CM000677.2:g.84654233C>G	GRCh38
NC_000015.9:g.85197464C>G , CM000677.1:g.85197464C>G	GRCh37
NC_000015.8:g.82998468C>G	NCBI36
NG_042034.1:g.5111G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032856.5:c.41+1G>C MANE Select	NP_116245.2:n.41+1G>C
ENST00000434634.7:c.41+1G>C MANE Select	ENSP00000387982.3:n.41+1G>C
NM_032856.3:c.41+1G>C	NP_116245.2:n.41+1G>C
NR_130944.1:n.14G>C
NR_130944.2:n.51G>C
NR_130945.1:n.110+1G>C
NR_130945.2:n.50+1G>C
NR_130946.1:n.111G>C
NR_130946.2:n.51G>C
NR_130947.1:n.110+1G>C
NR_130947.2:n.50+1G>C
ENST00000398528.7:n.111G>C
ENST00000434634.6:c.41+1G>C	ENSP00000387982.2:n.41+1G>C
ENST00000558019.5:n.51G>C
ENST00000558521.5:c.40+1G>C
ENST00000559015.5:n.47+1G>C
ENST00000559126.5:n.14G>C
ENST00000559178.5:c.25+1G>C
ENST00000559224.5:c.33+1G>C
ENST00000559452.5:n.40G>C
ENST00000559994.5:n.48G>C
ENST00000560182.5:n.9G>C
ENST00000560252.5:n.65+1G>C
ENST00000560835.5:n.51G>C
ENST00000561329.5:n.41+1G>C
ENST00000561434.1:n.58G>C
XR_001751407.2:n.50+1G>C
XR_001751408.2:n.57+1G>C
XR_243214.1:n.57+1G>C
XR_243214.3:n.57+1G>C