Canonical Allele Identifier: CA1542889

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19933415C>T , CM000664.2:g.19933415C>T	GRCh38
NC_000002.11:g.20133176C>T , CM000664.1:g.20133176C>T	GRCh37
NC_000002.10:g.19996657C>T	NCBI36
NG_021212.1:g.61709G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2644G>A MANE Select	NP_065830.2:p.Val882Ile
ENST00000281405.9:c.2644G>A MANE Select	ENSP00000281405.5:p.Val882Ile
NM_001006657.2:c.2677G>A MANE Plus Clinical	NP_001006658.1:p.Val893Ile
ENST00000345530.8:c.2677G>A MANE Plus Clinical	ENSP00000314444.5:p.Val893Ile
NM_001006657.1:c.2677G>A	NP_001006658.1:p.Val893Ile
NM_020779.3:c.2644G>A	NP_065830.2:p.Val882Ile
ENST00000281405.8:c.2644G>A	ENSP00000281405.4:p.Val882Ile
ENST00000345530.7:c.2677G>A	ENSP00000314444.5:p.Val893Ile
ENST00000414212.5:c.*59G>A	ENSP00000390802.1:n.*59G>A
ENST00000445063.5:c.2024-2006G>A
XM_011533007.1:c.1372G>A	XP_011531309.1:p.Val458Ile
XM_011533007.2:c.1372G>A	XP_011531309.1:p.Val458Ile
XR_001738862.1:n.2621G>A
XR_426989.2:n.2677G>A
XR_426989.3:n.2677G>A