Canonical Allele Identifier: CA1542692

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19914050T>C , CM000664.2:g.19914050T>C	GRCh38
NC_000002.11:g.20113811T>C , CM000664.1:g.20113811T>C	GRCh37
NC_000002.10:g.19977292T>C	NCBI36
NG_021212.1:g.81074A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.3349A>G MANE Select	NP_065830.2:p.Ser1117Gly
ENST00000281405.9:c.3349A>G MANE Select	ENSP00000281405.5:p.Ser1117Gly
NM_001006657.2:c.3382A>G MANE Plus Clinical	NP_001006658.1:p.Ser1128Gly
ENST00000345530.8:c.3382A>G MANE Plus Clinical	ENSP00000314444.5:p.Ser1128Gly
NM_001006657.1:c.3382A>G	NP_001006658.1:p.Ser1128Gly
NM_020779.3:c.3349A>G	NP_065830.2:p.Ser1117Gly
ENST00000281405.8:c.3349A>G	ENSP00000281405.4:p.Ser1117Gly
ENST00000345530.7:c.3382A>G	ENSP00000314444.5:p.Ser1128Gly
ENST00000414212.5:c.*664A>G	ENSP00000390802.1:n.*664A>G
ENST00000445063.5:c.2322-342A>G
XM_011533007.1:c.2077A>G	XP_011531309.1:p.Ser693Gly
XM_011533007.2:c.2077A>G	XP_011531309.1:p.Ser693Gly
XR_426989.3:n.3282A>G