Canonical Allele Identifier: CA345945083

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19946541G>C , CM000664.2:g.19946541G>C	GRCh38
NC_000002.11:g.20146302G>C , CM000664.1:g.20146302G>C	GRCh37
NC_000002.10:g.20009783G>C	NCBI36
NG_021212.1:g.48583C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1554C>G MANE Select	NP_065830.2:p.Tyr518Ter
ENST00000281405.9:c.1554C>G MANE Select	ENSP00000281405.5:p.Tyr518Ter
NM_001006657.2:c.1587C>G MANE Plus Clinical	NP_001006658.1:p.Tyr529Ter
ENST00000345530.8:c.1587C>G MANE Plus Clinical	ENSP00000314444.5:p.Tyr529Ter
NM_001006657.1:c.1587C>G	NP_001006658.1:p.Tyr529Ter
NM_020779.3:c.1554C>G	NP_065830.2:p.Tyr518Ter
ENST00000281405.8:c.1554C>G	ENSP00000281405.4:p.Tyr518Ter
ENST00000345530.7:c.1587C>G	ENSP00000314444.5:p.Tyr529Ter
ENST00000414212.5:c.1587C>G	ENSP00000390802.1:p.Tyr529Ter
ENST00000445063.5:c.1030C>G
ENST00000453014.1:c.192C>G	ENSP00000404409.1:p.Tyr64Ter
XM_011533007.1:c.282C>G	XP_011531309.1:p.Tyr94Ter
XM_011533007.2:c.282C>G	XP_011531309.1:p.Tyr94Ter
XR_001738862.1:n.1587C>G
XR_426989.2:n.1587C>G
XR_426989.3:n.1587C>G
XR_939699.1:n.1587C>G
XR_939699.3:n.1587C>G