Canonical Allele Identifier: CA2580064961

Gene: WDR35

Linked Data

• ClinVar Variation Id: 2177128
• ClinVar RCV Id: RCV002595122

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19931255A>T , CM000664.2:g.19931255A>T	GRCh38
NC_000002.11:g.20131016A>T , CM000664.1:g.20131016A>T	GRCh37
NC_000002.10:g.19994497A>T	NCBI36
NG_021212.1:g.63869T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.2964+14T>A MANE Select	ENSP00000281405.5:n.2964+14T>A
ENST00000345530.8:c.2997+14T>A MANE Plus Clinical	ENSP00000314444.5:n.2997+14T>A
ENST00000281405.8:c.2964+14T>A	ENSP00000281405.4:n.2964+14T>A
ENST00000345530.7:c.2997+14T>A	ENSP00000314444.5:n.2997+14T>A
ENST00000414212.5:c.*279+14T>A	ENSP00000390802.1:n.*279+14T>A
ENST00000445063.5:c.2164+14T>A
NM_001006657.1:c.2997+14T>A	NP_001006658.1:n.2997+14T>A
NM_020779.3:c.2964+14T>A	NP_065830.2:n.2964+14T>A
XM_011533007.1:c.1692+14T>A	XP_011531309.1:n.1692+14T>A
XR_426989.2:n.2897+14T>A
XM_011533007.2:c.1692+14T>A	XP_011531309.1:n.1692+14T>A
XR_426989.3:n.2897+14T>A
NM_001006657.2:c.2997+14T>A MANE Plus Clinical	NP_001006658.1:n.2997+14T>A
NM_020779.4:c.2964+14T>A MANE Select	NP_065830.2:n.2964+14T>A