Canonical Allele Identifier: CA345942957

Gene: WDR35

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19935529T>A , CM000664.2:g.19935529T>A	GRCh38
NC_000002.11:g.20135290T>A , CM000664.1:g.20135290T>A	GRCh37
NC_000002.10:g.19998771T>A	NCBI36
NG_021212.1:g.59595A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.2489A>T MANE Select	ENSP00000281405.5:p.Asp830Val
ENST00000345530.8:c.2522A>T MANE Plus Clinical	ENSP00000314444.5:p.Asp841Val
ENST00000281405.8:c.2489A>T	ENSP00000281405.4:p.Asp830Val
ENST00000345530.7:c.2522A>T	ENSP00000314444.5:p.Asp841Val
ENST00000414212.5:c.2522A>T	ENSP00000390802.1:p.Asp841Val
ENST00000445063.5:c.1965A>T
ENST00000453014.1:c.1127A>T	ENSP00000404409.1:p.Asp376Val
NM_001006657.1:c.2522A>T	NP_001006658.1:p.Asp841Val
NM_020779.3:c.2489A>T	NP_065830.2:p.Asp830Val
XM_011533007.1:c.1217A>T	XP_011531309.1:p.Asp406Val
XR_426989.2:n.2522A>T
XM_011533007.2:c.1217A>T	XP_011531309.1:p.Asp406Val
XR_001738862.1:n.2466A>T
XR_426989.3:n.2522A>T
NM_001006657.2:c.2522A>T MANE Plus Clinical	NP_001006658.1:p.Asp841Val
NM_020779.4:c.2489A>T MANE Select	NP_065830.2:p.Asp830Val