Canonical Allele Identifier: CA345948506
Gene: WDR35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19989194A>C , CM000664.2:g.19989194A>C GRCh38
NC_000002.11:g.20188955A>C , CM000664.1:g.20188955A>C GRCh37
NC_000002.10:g.20052436A>C NCBI36
NG_021212.1:g.5930T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.113T>G MANE Select ENSP00000281405.5:p.Leu38Arg
ENST00000345530.8:c.113T>G MANE Plus Clinical ENSP00000314444.5:p.Leu38Arg
ENST00000281405.8:c.113T>G ENSP00000281405.4:p.Leu38Arg
ENST00000345530.7:c.113T>G ENSP00000314444.5:p.Leu38Arg
ENST00000414212.5:c.113T>G ENSP00000390802.1:p.Leu38Arg
NM_001006657.1:c.113T>G NP_001006658.1:p.Leu38Arg
NM_020779.3:c.113T>G NP_065830.2:p.Leu38Arg
XR_426989.2:n.146T>G
XR_939699.1:n.146T>G
XR_001738862.1:n.146T>G
XR_426989.3:n.146T>G
XR_939699.3:n.146T>G
NM_001006657.2:c.113T>G MANE Plus Clinical NP_001006658.1:p.Leu38Arg
NM_020779.4:c.113T>G MANE Select NP_065830.2:p.Leu38Arg