Canonical Allele Identifier: CA1543133

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19945941G>A , CM000664.2:g.19945941G>A	GRCh38
NC_000002.11:g.20145702G>A , CM000664.1:g.20145702G>A	GRCh37
NC_000002.10:g.20009183G>A	NCBI36
NG_021212.1:g.49183C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1690C>T MANE Select	NP_065830.2:p.Arg564Ter
ENST00000281405.9:c.1690C>T MANE Select	ENSP00000281405.5:p.Arg564Ter
NM_001006657.2:c.1723C>T MANE Plus Clinical	NP_001006658.1:p.Arg575Ter
ENST00000345530.8:c.1723C>T MANE Plus Clinical	ENSP00000314444.5:p.Arg575Ter
NM_001006657.1:c.1723C>T	NP_001006658.1:p.Arg575Ter
NM_020779.3:c.1690C>T	NP_065830.2:p.Arg564Ter
ENST00000281405.8:c.1690C>T	ENSP00000281405.4:p.Arg564Ter
ENST00000345530.7:c.1723C>T	ENSP00000314444.5:p.Arg575Ter
ENST00000414212.5:c.1723C>T	ENSP00000390802.1:p.Arg575Ter
ENST00000445063.5:c.1166C>T
ENST00000453014.1:c.328C>T	ENSP00000404409.1:p.Arg110Ter
XM_011533007.1:c.418C>T	XP_011531309.1:p.Arg140Ter
XM_011533007.2:c.418C>T	XP_011531309.1:p.Arg140Ter
XR_001738862.1:n.1723C>T
XR_426989.2:n.1723C>T
XR_426989.3:n.1723C>T
XR_939699.1:n.1723C>T
XR_939699.3:n.1723C>T