Canonical Allele Identifier: CA10611913

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19913035C>T , CM000664.2:g.19913035C>T	GRCh38
NC_000002.11:g.20112796C>T , CM000664.1:g.20112796C>T	GRCh37
NC_000002.10:g.19976277C>T	NCBI36
NG_021212.1:g.82089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.*523G>A MANE Select	ENSP00000281405.5:n.*523G>A
ENST00000345530.8:c.*523G>A MANE Plus Clinical	ENSP00000314444.5:n.*523G>A
ENST00000281405.8:c.*523G>A	ENSP00000281405.4:n.*523G>A
ENST00000345530.7:c.*523G>A	ENSP00000314444.5:n.*523G>A
NM_001006657.1:c.*523G>A	NP_001006658.1:n.*523G>A
NM_020779.3:c.*523G>A	NP_065830.2:n.*523G>A
XM_011533007.1:c.*523G>A	XP_011531309.1:n.*523G>A
XM_011533007.2:c.*523G>A	XP_011531309.1:n.*523G>A
XR_426989.3:n.3969G>A
NM_001006657.2:c.*523G>A MANE Plus Clinical	NP_001006658.1:n.*523G>A
NM_020779.4:c.*523G>A MANE Select	NP_065830.2:n.*523G>A