Canonical Allele Identifier: CA1543506

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19975602C>T , CM000664.2:g.19975602C>T	GRCh38
NC_000002.11:g.20175363C>T , CM000664.1:g.20175363C>T	GRCh37
NC_000002.10:g.20038844C>T	NCBI36
NG_021212.1:g.19522G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.498G>A MANE Select	NP_065830.2:p.Ala166=
ENST00000281405.9:c.498G>A MANE Select	ENSP00000281405.5:p.Ala166=
NM_001006657.2:c.498G>A MANE Plus Clinical	NP_001006658.1:p.Ala166=
ENST00000345530.8:c.498G>A MANE Plus Clinical	ENSP00000314444.5:p.Ala166=
NM_001006657.1:c.498G>A	NP_001006658.1:p.Ala166=
NM_020779.3:c.498G>A	NP_065830.2:p.Ala166=
ENST00000281405.8:c.498G>A	ENSP00000281405.4:p.Ala166=
ENST00000345530.7:c.498G>A	ENSP00000314444.5:p.Ala166=
ENST00000414212.5:c.498G>A	ENSP00000390802.1:p.Ala166=
ENST00000445063.5:c.35G>A
XR_001738862.1:n.531G>A
XR_426989.2:n.531G>A
XR_426989.3:n.531G>A
XR_939699.1:n.531G>A
XR_939699.3:n.531G>A