Canonical Allele Identifier: CA1543244

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19953831T>C , CM000664.2:g.19953831T>C	GRCh38
NC_000002.11:g.20153592T>C , CM000664.1:g.20153592T>C	GRCh37
NC_000002.10:g.20017073T>C	NCBI36
NG_021212.1:g.41293A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.1400+3A>G MANE Select	ENSP00000281405.5:n.1400+3A>G
ENST00000345530.8:c.1433+3A>G MANE Plus Clinical	ENSP00000314444.5:n.1433+3A>G
ENST00000281405.8:c.1400+3A>G	ENSP00000281405.4:n.1400+3A>G
ENST00000345530.7:c.1433+3A>G	ENSP00000314444.5:n.1433+3A>G
ENST00000414212.5:c.1433+3A>G	ENSP00000390802.1:n.1433+3A>G
ENST00000445063.5:c.876+3A>G
ENST00000453014.1:c.38+3A>G	ENSP00000404409.1:n.38+3A>G
NM_001006657.1:c.1433+3A>G	NP_001006658.1:n.1433+3A>G
NM_020779.3:c.1400+3A>G	NP_065830.2:n.1400+3A>G
XM_011533007.1:c.128+3A>G	XP_011531309.1:n.128+3A>G
XR_426989.2:n.1433+3A>G
XR_939699.1:n.1433+3A>G
XM_011533007.2:c.128+3A>G	XP_011531309.1:n.128+3A>G
XR_001738862.1:n.1433+3A>G
XR_426989.3:n.1433+3A>G
XR_939699.3:n.1433+3A>G
NM_001006657.2:c.1433+3A>G MANE Plus Clinical	NP_001006658.1:n.1433+3A>G
NM_020779.4:c.1400+3A>G MANE Select	NP_065830.2:n.1400+3A>G