Canonical Allele Identifier: CA1542761

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19930491G>C , CM000664.2:g.19930491G>C	GRCh38
NC_000002.11:g.20130252G>C , CM000664.1:g.20130252G>C	GRCh37
NC_000002.10:g.19993733G>C	NCBI36
NG_021212.1:g.64633C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.3026C>G MANE Select	NP_065830.2:p.Thr1009Arg
ENST00000281405.9:c.3026C>G MANE Select	ENSP00000281405.5:p.Thr1009Arg
NM_001006657.2:c.3059C>G MANE Plus Clinical	NP_001006658.1:p.Thr1020Arg
ENST00000345530.8:c.3059C>G MANE Plus Clinical	ENSP00000314444.5:p.Thr1020Arg
NM_001006657.1:c.3059C>G	NP_001006658.1:p.Thr1020Arg
NM_020779.3:c.3026C>G	NP_065830.2:p.Thr1009Arg
ENST00000281405.8:c.3026C>G	ENSP00000281405.4:p.Thr1009Arg
ENST00000345530.7:c.3059C>G	ENSP00000314444.5:p.Thr1020Arg
ENST00000414212.5:c.*341C>G	ENSP00000390802.1:n.*341C>G
ENST00000445063.5:c.2226C>G
XM_011533007.1:c.1754C>G	XP_011531309.1:p.Thr585Arg
XM_011533007.2:c.1754C>G	XP_011531309.1:p.Thr585Arg
XR_426989.2:n.2959C>G
XR_426989.3:n.2959C>G