Canonical Allele Identifier: CA206270

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19951450T>C , CM000664.2:g.19951450T>C	GRCh38
NC_000002.11:g.20151211T>C , CM000664.1:g.20151211T>C	GRCh37
NC_000002.10:g.20014692T>C	NCBI36
NG_021212.1:g.43674A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1435A>G MANE Select	NP_065830.2:p.Met479Val
ENST00000281405.9:c.1435A>G MANE Select	ENSP00000281405.5:p.Met479Val
NM_001006657.2:c.1468A>G MANE Plus Clinical	NP_001006658.1:p.Met490Val
ENST00000345530.8:c.1468A>G MANE Plus Clinical	ENSP00000314444.5:p.Met490Val
NM_001006657.1:c.1468A>G	NP_001006658.1:p.Met490Val
NM_020779.3:c.1435A>G	NP_065830.2:p.Met479Val
ENST00000281405.8:c.1435A>G	ENSP00000281405.4:p.Met479Val
ENST00000345530.7:c.1468A>G	ENSP00000314444.5:p.Met490Val
ENST00000414212.5:c.1468A>G	ENSP00000390802.1:p.Met490Val
ENST00000445063.5:c.911A>G
ENST00000453014.1:c.73A>G	ENSP00000404409.1:p.Met25Val
ENST00000494964.1:n.472A>G
XM_011533007.1:c.163A>G	XP_011531309.1:p.Met55Val
XM_011533007.2:c.163A>G	XP_011531309.1:p.Met55Val
XR_001738862.1:n.1468A>G
XR_426989.2:n.1468A>G
XR_426989.3:n.1468A>G
XR_939699.1:n.1468A>G
XR_939699.3:n.1468A>G