Canonical Allele Identifier: CA345941633
Gene: WDR35 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19930483C>G , CM000664.2:g.19930483C>G GRCh38
NC_000002.11:g.20130244C>G , CM000664.1:g.20130244C>G GRCh37
NC_000002.10:g.19993725C>G NCBI36
NG_021212.1:g.64641G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.3034G>C MANE Select ENSP00000281405.5:p.Ala1012Pro
ENST00000345530.8:c.3067G>C MANE Plus Clinical ENSP00000314444.5:p.Ala1023Pro
ENST00000281405.8:c.3034G>C ENSP00000281405.4:p.Ala1012Pro
ENST00000345530.7:c.3067G>C ENSP00000314444.5:p.Ala1023Pro
ENST00000414212.5:c.*349G>C ENSP00000390802.1:n.*349G>C
ENST00000445063.5:c.2234G>C
NM_001006657.1:c.3067G>C NP_001006658.1:p.Ala1023Pro
NM_020779.3:c.3034G>C NP_065830.2:p.Ala1012Pro
XM_011533007.1:c.1762G>C XP_011531309.1:p.Ala588Pro
XR_426989.2:n.2967G>C
XM_011533007.2:c.1762G>C XP_011531309.1:p.Ala588Pro
XR_426989.3:n.2967G>C
NM_001006657.2:c.3067G>C MANE Plus Clinical NP_001006658.1:p.Ala1023Pro
NM_020779.4:c.3034G>C MANE Select NP_065830.2:p.Ala1012Pro