Canonical Allele Identifier: CA1542905

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19933486A>G , CM000664.2:g.19933486A>G	GRCh38
NC_000002.11:g.20133247A>G , CM000664.1:g.20133247A>G	GRCh37
NC_000002.10:g.19996728A>G	NCBI36
NG_021212.1:g.61638T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2573T>C MANE Select	NP_065830.2:p.Val858Ala
ENST00000281405.9:c.2573T>C MANE Select	ENSP00000281405.5:p.Val858Ala
NM_001006657.2:c.2606T>C MANE Plus Clinical	NP_001006658.1:p.Val869Ala
ENST00000345530.8:c.2606T>C MANE Plus Clinical	ENSP00000314444.5:p.Val869Ala
NM_001006657.1:c.2606T>C	NP_001006658.1:p.Val869Ala
NM_020779.3:c.2573T>C	NP_065830.2:p.Val858Ala
ENST00000281405.8:c.2573T>C	ENSP00000281405.4:p.Val858Ala
ENST00000345530.7:c.2606T>C	ENSP00000314444.5:p.Val869Ala
ENST00000414212.5:c.2610T>C	ENSP00000390802.1:p.Ser870=
ENST00000445063.5:c.2023+1985T>C
XM_011533007.1:c.1301T>C	XP_011531309.1:p.Val434Ala
XM_011533007.2:c.1301T>C	XP_011531309.1:p.Val434Ala
XR_001738862.1:n.2550T>C
XR_426989.2:n.2606T>C
XR_426989.3:n.2606T>C