Canonical Allele Identifier: CA346230407

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19913576G>T , CM000664.2:g.19913576G>T	GRCh38
NC_000002.11:g.20113337G>T , CM000664.1:g.20113337G>T	GRCh37
NC_000002.10:g.19976818G>T	NCBI36
NG_021212.1:g.81548C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.3495C>A MANE Select	NP_065830.2:p.Cys1165Ter
ENST00000281405.9:c.3495C>A MANE Select	ENSP00000281405.5:p.Cys1165Ter
NM_001006657.2:c.3528C>A MANE Plus Clinical	NP_001006658.1:p.Cys1176Ter
ENST00000345530.8:c.3528C>A MANE Plus Clinical	ENSP00000314444.5:p.Cys1176Ter
NM_001006657.1:c.3528C>A	NP_001006658.1:p.Cys1176Ter
NM_020779.3:c.3495C>A	NP_065830.2:p.Cys1165Ter
ENST00000281405.8:c.3495C>A	ENSP00000281405.4:p.Cys1165Ter
ENST00000345530.7:c.3528C>A	ENSP00000314444.5:p.Cys1176Ter
ENST00000414212.5:c.*810C>A	ENSP00000390802.1:n.*810C>A
ENST00000445063.5:c.2454C>A
XM_011533007.1:c.2223C>A	XP_011531309.1:p.Cys741Ter
XM_011533007.2:c.2223C>A	XP_011531309.1:p.Cys741Ter
XR_426989.3:n.3428C>A