Canonical Allele Identifier: CA249845

Gene: WDR73

Linked Data

• ClinVar Variation Id: 208470
• ClinVar RCV Id: RCV000190493 ; RCV000657966 ; RCV001849333
• dbSNP Id: rs797044995
• gnomAD v4: 15-84648537-C-T
• MyVariant Identifiers: chr15:g.85191768C>T (hg19) ; chr15:g.84648537C>T (hg38)
• PubMed: PMID:26123727

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84648537C>T , CM000677.2:g.84648537C>T	GRCh38
NC_000015.9:g.85191768C>T , CM000677.1:g.85191768C>T	GRCh37
NC_000015.8:g.82992772C>T	NCBI36
NG_042034.1:g.10807G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434634.7:c.287G>A MANE Select	ENSP00000387982.3:p.Arg96Lys
ENST00000398528.7:n.363G>A
ENST00000434634.6:c.287G>A	ENSP00000387982.2:p.Arg96Lys
ENST00000558019.5:n.303G>A
ENST00000558487.1:n.547G>A
ENST00000558521.5:c.286G>A
ENST00000558608.1:n.50G>A
ENST00000559015.5:n.293G>A
ENST00000559126.5:n.793G>A
ENST00000559178.5:c.271G>A
ENST00000559224.5:c.191-583G>A
ENST00000559452.5:n.751G>A
ENST00000559877.5:n.479G>A
ENST00000559994.5:n.300G>A
ENST00000560088.5:n.297G>A
ENST00000560182.5:n.462G>A
ENST00000560252.5:n.311G>A
ENST00000560835.5:n.303G>A
ENST00000560966.5:n.1489G>A
ENST00000561329.5:n.287G>A
ENST00000561447.5:n.452G>A
NM_032856.3:c.287G>A	NP_116245.2:p.Arg96Lys
NR_130944.1:n.793G>A
NR_130945.1:n.356G>A
NR_130946.1:n.363G>A
NR_130947.1:n.268-583G>A
XR_243214.1:n.303G>A
XR_001751407.2:n.296G>A
XR_001751408.2:n.303G>A
XR_243214.3:n.303G>A
NM_032856.5:c.287G>A MANE Select	NP_116245.2:p.Arg96Lys
NR_130944.2:n.830G>A
NR_130945.2:n.296G>A
NR_130946.2:n.303G>A
NR_130947.2:n.208-583G>A