Canonical Allele Identifier: CA1542823

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19931391T>A , CM000664.2:g.19931391T>A	GRCh38
NC_000002.11:g.20131152T>A , CM000664.1:g.20131152T>A	GRCh37
NC_000002.10:g.19994633T>A	NCBI36
NG_021212.1:g.63733A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2842A>T MANE Select	NP_065830.2:p.Lys948Ter
ENST00000281405.9:c.2842A>T MANE Select	ENSP00000281405.5:p.Lys948Ter
NM_001006657.2:c.2875A>T MANE Plus Clinical	NP_001006658.1:p.Lys959Ter
ENST00000345530.8:c.2875A>T MANE Plus Clinical	ENSP00000314444.5:p.Lys959Ter
NM_001006657.1:c.2875A>T	NP_001006658.1:p.Lys959Ter
NM_020779.3:c.2842A>T	NP_065830.2:p.Lys948Ter
ENST00000281405.8:c.2842A>T	ENSP00000281405.4:p.Lys948Ter
ENST00000345530.7:c.2875A>T	ENSP00000314444.5:p.Lys959Ter
ENST00000414212.5:c.*157A>T	ENSP00000390802.1:n.*157A>T
ENST00000445063.5:c.2042A>T
XM_011533007.1:c.1570A>T	XP_011531309.1:p.Lys524Ter
XM_011533007.2:c.1570A>T	XP_011531309.1:p.Lys524Ter
XR_426989.2:n.2775A>T
XR_426989.3:n.2775A>T