Canonical Allele Identifier: CA1543272

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19953974T>C , CM000664.2:g.19953974T>C	GRCh38
NC_000002.11:g.20153735T>C , CM000664.1:g.20153735T>C	GRCh37
NC_000002.10:g.20017216T>C	NCBI36
NG_021212.1:g.41150A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1260A>G MANE Select	NP_065830.2:p.Pro420=
ENST00000281405.9:c.1260A>G MANE Select	ENSP00000281405.5:p.Pro420=
NM_001006657.2:c.1293A>G MANE Plus Clinical	NP_001006658.1:p.Pro431=
ENST00000345530.8:c.1293A>G MANE Plus Clinical	ENSP00000314444.5:p.Pro431=
NM_001006657.1:c.1293A>G	NP_001006658.1:p.Pro431=
NM_020779.3:c.1260A>G	NP_065830.2:p.Pro420=
ENST00000281405.8:c.1260A>G	ENSP00000281405.4:p.Pro420=
ENST00000345530.7:c.1293A>G	ENSP00000314444.5:p.Pro431=
ENST00000414212.5:c.1293A>G	ENSP00000390802.1:p.Pro431=
ENST00000445063.5:c.736A>G
XM_011533007.1:c.-13A>G	XP_011531309.1:n.-13A>G
XM_011533007.2:c.-13A>G	XP_011531309.1:n.-13A>G
XR_001738862.1:n.1293A>G
XR_426989.2:n.1293A>G
XR_426989.3:n.1293A>G
XR_939699.1:n.1293A>G
XR_939699.3:n.1293A>G