Canonical Allele Identifier: CA346231401

Gene: WDR35

Linked Data

• MyVariant Identifiers: chr2:g.20113881C>A (hg19) ; chr2:g.19914120C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19914120C>A , CM000664.2:g.19914120C>A	GRCh38
NC_000002.11:g.20113881C>A , CM000664.1:g.20113881C>A	GRCh37
NC_000002.10:g.19977362C>A	NCBI36
NG_021212.1:g.81004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.3279G>T MANE Select	ENSP00000281405.5:p.Gln1093His
ENST00000345530.8:c.3312G>T MANE Plus Clinical	ENSP00000314444.5:p.Gln1104His
ENST00000281405.8:c.3279G>T	ENSP00000281405.4:p.Gln1093His
ENST00000345530.7:c.3312G>T	ENSP00000314444.5:p.Gln1104His
ENST00000414212.5:c.*594G>T	ENSP00000390802.1:n.*594G>T
ENST00000445063.5:c.2322-412G>T
NM_001006657.1:c.3312G>T	NP_001006658.1:p.Gln1104His
NM_020779.3:c.3279G>T	NP_065830.2:p.Gln1093His
XM_011533007.1:c.2007G>T	XP_011531309.1:p.Gln669His
XM_011533007.2:c.2007G>T	XP_011531309.1:p.Gln669His
XR_426989.3:n.3212G>T
NM_001006657.2:c.3312G>T MANE Plus Clinical	NP_001006658.1:p.Gln1104His
NM_020779.4:c.3279G>T MANE Select	NP_065830.2:p.Gln1093His