Canonical Allele Identifier: CA1543553

Gene: WDR35

Linked Data

• ClinVar Variation Id: 281109
• ClinVar RCV Id: RCV000280618 ; RCV000356360 ; RCV000375021 ; RCV001085930 ; RCV000767100 ; RCV004535250
• dbSNP Id: rs140308808
• ExAC: 2:20178593 G / A
• gnomAD v2: 2-20178593-G-A
• gnomAD v3: 2-19978832-G-A
• gnomAD v4: 2-19978832-G-A
• MyVariant Identifiers: chr2:g.20178593G>A (hg19) ; chr2:g.19978832G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19978832G>A , CM000664.2:g.19978832G>A	GRCh38
NC_000002.11:g.20178593G>A , CM000664.1:g.20178593G>A	GRCh37
NC_000002.10:g.20042074G>A	NCBI36
NG_021212.1:g.16292C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.355C>T MANE Select	ENSP00000281405.5:p.Arg119Cys
ENST00000345530.8:c.355C>T MANE Plus Clinical	ENSP00000314444.5:p.Arg119Cys
ENST00000281405.8:c.355C>T	ENSP00000281405.4:p.Arg119Cys
ENST00000345530.7:c.355C>T	ENSP00000314444.5:p.Arg119Cys
ENST00000414212.5:c.355C>T	ENSP00000390802.1:p.Arg119Cys
NM_001006657.1:c.355C>T	NP_001006658.1:p.Arg119Cys
NM_020779.3:c.355C>T	NP_065830.2:p.Arg119Cys
XR_426989.2:n.388C>T
XR_939699.1:n.388C>T
XR_001738862.1:n.388C>T
XR_426989.3:n.388C>T
XR_939699.3:n.388C>T
NM_001006657.2:c.355C>T MANE Plus Clinical	NP_001006658.1:p.Arg119Cys
NM_020779.4:c.355C>T MANE Select	NP_065830.2:p.Arg119Cys