Canonical Allele Identifier: CA2492981421

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19941796A= , CM000664.2:g.19941796A=	GRCh38
NC_000002.11:g.20141557A= , CM000664.1:g.20141557A=	GRCh37
NC_000002.10:g.20005038A=	NCBI36
NG_021212.1:g.53328T=

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1889T= MANE Select	NP_065830.2:p.Leu630=
ENST00000281405.9:c.1889T= MANE Select	ENSP00000281405.5:p.Leu630=
NM_001006657.2:c.1922T= MANE Plus Clinical	NP_001006658.1:p.Leu641=
ENST00000345530.8:c.1922T= MANE Plus Clinical	ENSP00000314444.5:p.Leu641=
NM_001006657.1:c.1922T=	NP_001006658.1:p.Leu641=
NM_020779.3:c.1889T=	NP_065830.2:p.Leu630=
ENST00000281405.8:c.1889T=	ENSP00000281405.4:p.Leu630=
ENST00000345530.7:c.1922T=	ENSP00000314444.5:p.Leu641=
ENST00000414212.5:c.1922T=	ENSP00000390802.1:p.Leu641=
ENST00000445063.5:c.1365T=
ENST00000453014.1:c.527T=	ENSP00000404409.1:p.Leu176=
XM_011533007.1:c.617T=	XP_011531309.1:p.Leu206=
XM_011533007.2:c.617T=	XP_011531309.1:p.Leu206=
XR_001738862.1:n.1922T=
XR_426989.2:n.1922T=
XR_426989.3:n.1922T=
XR_939699.1:n.1879-71T=
XR_939699.3:n.1879-71T=