Canonical Allele Identifier: CA1542820

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19931370G>A , CM000664.2:g.19931370G>A	GRCh38
NC_000002.11:g.20131131G>A , CM000664.1:g.20131131G>A	GRCh37
NC_000002.10:g.19994612G>A	NCBI36
NG_021212.1:g.63754C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2863C>T MANE Select	NP_065830.2:p.Arg955Cys
ENST00000281405.9:c.2863C>T MANE Select	ENSP00000281405.5:p.Arg955Cys
NM_001006657.2:c.2896C>T MANE Plus Clinical	NP_001006658.1:p.Arg966Cys
ENST00000345530.8:c.2896C>T MANE Plus Clinical	ENSP00000314444.5:p.Arg966Cys
NM_001006657.1:c.2896C>T	NP_001006658.1:p.Arg966Cys
NM_020779.3:c.2863C>T	NP_065830.2:p.Arg955Cys
ENST00000281405.8:c.2863C>T	ENSP00000281405.4:p.Arg955Cys
ENST00000345530.7:c.2896C>T	ENSP00000314444.5:p.Arg966Cys
ENST00000414212.5:c.*178C>T	ENSP00000390802.1:n.*178C>T
ENST00000445063.5:c.2063C>T
XM_011533007.1:c.1591C>T	XP_011531309.1:p.Arg531Cys
XM_011533007.2:c.1591C>T	XP_011531309.1:p.Arg531Cys
XR_426989.2:n.2796C>T
XR_426989.3:n.2796C>T