Canonical Allele Identifier: CA345945624

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19953912C>T , CM000664.2:g.19953912C>T	GRCh38
NC_000002.11:g.20153673C>T , CM000664.1:g.20153673C>T	GRCh37
NC_000002.10:g.20017154C>T	NCBI36
NG_021212.1:g.41212G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1322G>A MANE Select	NP_065830.2:p.Trp441Ter
ENST00000281405.9:c.1322G>A MANE Select	ENSP00000281405.5:p.Trp441Ter
NM_001006657.2:c.1355G>A MANE Plus Clinical	NP_001006658.1:p.Trp452Ter
ENST00000345530.8:c.1355G>A MANE Plus Clinical	ENSP00000314444.5:p.Trp452Ter
NM_001006657.1:c.1355G>A	NP_001006658.1:p.Trp452Ter
NM_020779.3:c.1322G>A	NP_065830.2:p.Trp441Ter
ENST00000281405.8:c.1322G>A	ENSP00000281405.4:p.Trp441Ter
ENST00000345530.7:c.1355G>A	ENSP00000314444.5:p.Trp452Ter
ENST00000414212.5:c.1355G>A	ENSP00000390802.1:p.Trp452Ter
ENST00000445063.5:c.798G>A
XM_011533007.1:c.50G>A	XP_011531309.1:p.Trp17Ter
XM_011533007.2:c.50G>A	XP_011531309.1:p.Trp17Ter
XR_001738862.1:n.1355G>A
XR_426989.2:n.1355G>A
XR_426989.3:n.1355G>A
XR_939699.1:n.1355G>A
XR_939699.3:n.1355G>A