Canonical Allele Identifier: CA055994

Gene: WDR73

Linked Data

• ClinVar Variation Id: 242543
• ClinVar RCV Id: RCV000785981
• dbSNP Id: rs863223396
• MyVariant Identifiers: chr15:g.85191180A>G (hg19) ; chr15:g.84647949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84647949A>G , CM000677.2:g.84647949A>G	GRCh38
NC_000015.9:g.85191180A>G , CM000677.1:g.85191180A>G	GRCh37
NC_000015.8:g.82992184A>G	NCBI36
NG_042034.1:g.11395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434634.7:c.293T>C MANE Select	ENSP00000387982.3:p.Leu98Pro
ENST00000398528.7:n.369T>C
ENST00000434634.6:c.293T>C	ENSP00000387982.2:p.Leu98Pro
ENST00000558521.5:c.292T>C
ENST00000558608.1:n.638T>C
ENST00000559015.5:n.881T>C
ENST00000559126.5:n.799T>C
ENST00000559178.5:c.277T>C
ENST00000559224.5:c.196T>C
ENST00000559452.5:n.757T>C
ENST00000559994.5:n.306T>C
ENST00000560088.5:n.303T>C
ENST00000560252.5:n.317T>C
ENST00000560835.5:n.309T>C
ENST00000560966.5:n.2077T>C
ENST00000561329.5:n.293T>C
ENST00000561447.5:n.458T>C
NM_032856.3:c.293T>C	NP_116245.2:p.Leu98Pro
NR_130944.1:n.799T>C
NR_130945.1:n.362T>C
NR_130946.1:n.369T>C
NR_130947.1:n.273T>C
XR_243214.1:n.309T>C
XR_001751407.2:n.302T>C
XR_001751408.2:n.309T>C
XR_243214.3:n.309T>C
NM_032856.5:c.293T>C MANE Select	NP_116245.2:p.Leu98Pro
NR_130944.2:n.836T>C
NR_130945.2:n.302T>C
NR_130946.2:n.309T>C
NR_130947.2:n.213T>C