Canonical Allele Identifier: CA249841

Gene: WDR73

Linked Data

• ClinVar Variation Id: 208468
• ClinVar RCV Id: RCV000190491 ; RCV000414279
• dbSNP Id: rs797044993
• gnomAD v2: 15-85196904-A-T
• gnomAD v4: 15-84653673-A-T
• MyVariant Identifiers: chr15:g.85196904A>T (hg19) ; chr15:g.84653673A>T (hg38)
• PubMed: PMID:26123727

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84653673A>T , CM000677.2:g.84653673A>T	GRCh38
NC_000015.9:g.85196904A>T , CM000677.1:g.85196904A>T	GRCh37
NC_000015.8:g.82997908A>T	NCBI36
NG_042034.1:g.5671T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434634.7:c.68T>A MANE Select	ENSP00000387982.3:p.Leu23Gln
ENST00000398528.7:n.144T>A
ENST00000434634.6:c.68T>A	ENSP00000387982.2:p.Leu23Gln
ENST00000558019.5:n.84T>A
ENST00000558487.1:n.328T>A
ENST00000558521.5:c.67T>A
ENST00000559015.5:n.74T>A
ENST00000559126.5:n.574T>A
ENST00000559178.5:c.52T>A
ENST00000559224.5:c.60T>A
ENST00000559452.5:n.573+27T>A
ENST00000559877.5:n.301+27T>A
ENST00000559994.5:n.81T>A
ENST00000560088.5:n.78T>A
ENST00000560182.5:n.243T>A
ENST00000560252.5:n.92T>A
ENST00000560835.5:n.84T>A
ENST00000560966.5:n.559T>A
ENST00000561329.5:n.68T>A
ENST00000561434.1:n.91T>A
ENST00000561447.5:n.233T>A
NM_032856.3:c.68T>A	NP_116245.2:p.Leu23Gln
NR_130944.1:n.574T>A
NR_130945.1:n.137T>A
NR_130946.1:n.144T>A
NR_130947.1:n.137T>A
XR_243214.1:n.84T>A
XR_001751407.2:n.77T>A
XR_001751408.2:n.84T>A
XR_243214.3:n.84T>A
NM_032856.5:c.68T>A MANE Select	NP_116245.2:p.Leu23Gln
NR_130944.2:n.611T>A
NR_130945.2:n.77T>A
NR_130946.2:n.84T>A
NR_130947.2:n.77T>A