Canonical Allele Identifier: CA1543135

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19945969T>A , CM000664.2:g.19945969T>A	GRCh38
NC_000002.11:g.20145730T>A , CM000664.1:g.20145730T>A	GRCh37
NC_000002.10:g.20009211T>A	NCBI36
NG_021212.1:g.49155A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1662A>T MANE Select	NP_065830.2:p.Gly554=
ENST00000281405.9:c.1662A>T MANE Select	ENSP00000281405.5:p.Gly554=
NM_001006657.2:c.1695A>T MANE Plus Clinical	NP_001006658.1:p.Gly565=
ENST00000345530.8:c.1695A>T MANE Plus Clinical	ENSP00000314444.5:p.Gly565=
NM_001006657.1:c.1695A>T	NP_001006658.1:p.Gly565=
NM_020779.3:c.1662A>T	NP_065830.2:p.Gly554=
ENST00000281405.8:c.1662A>T	ENSP00000281405.4:p.Gly554=
ENST00000345530.7:c.1695A>T	ENSP00000314444.5:p.Gly565=
ENST00000414212.5:c.1695A>T	ENSP00000390802.1:p.Gly565=
ENST00000445063.5:c.1138A>T
ENST00000453014.1:c.300A>T	ENSP00000404409.1:p.Gly100=
XM_011533007.1:c.390A>T	XP_011531309.1:p.Gly130=
XM_011533007.2:c.390A>T	XP_011531309.1:p.Gly130=
XR_001738862.1:n.1695A>T
XR_426989.2:n.1695A>T
XR_426989.3:n.1695A>T
XR_939699.1:n.1695A>T
XR_939699.3:n.1695A>T