Canonical Allele Identifier: CA43409423

Gene: WDR35

Linked Data

• ClinVar Variation Id: 440415
• ClinVar RCV Id: RCV000507316
• dbSNP Id: rs192330354
• gnomAD v2: 2-20151045-A-T
• gnomAD v3: 2-19951284-A-T
• gnomAD v4: 2-19951284-A-T
• MyVariant Identifiers: chr2:g.20151045A>T (hg19) ; chr2:g.19951284A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19951284A>T , CM000664.2:g.19951284A>T	GRCh38
NC_000002.11:g.20151045A>T , CM000664.1:g.20151045A>T	GRCh37
NC_000002.10:g.20014526A>T	NCBI36
NG_021212.1:g.43840T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.1470+131T>A MANE Select	ENSP00000281405.5:n.1470+131T>A
ENST00000345530.8:c.1503+131T>A MANE Plus Clinical	ENSP00000314444.5:n.1503+131T>A
ENST00000281405.8:c.1470+131T>A	ENSP00000281405.4:n.1470+131T>A
ENST00000345530.7:c.1503+131T>A	ENSP00000314444.5:n.1503+131T>A
ENST00000414212.5:c.1503+131T>A	ENSP00000390802.1:n.1503+131T>A
ENST00000445063.5:c.946+131T>A
ENST00000453014.1:c.108+131T>A	ENSP00000404409.1:n.108+131T>A
ENST00000494964.1:n.507+131T>A
NM_001006657.1:c.1503+131T>A	NP_001006658.1:n.1503+131T>A
NM_020779.3:c.1470+131T>A	NP_065830.2:n.1470+131T>A
XM_011533007.1:c.198+131T>A	XP_011531309.1:n.198+131T>A
XR_426989.2:n.1503+131T>A
XR_939699.1:n.1503+131T>A
XM_011533007.2:c.198+131T>A	XP_011531309.1:n.198+131T>A
XR_001738862.1:n.1503+131T>A
XR_426989.3:n.1503+131T>A
XR_939699.3:n.1503+131T>A
NM_001006657.2:c.1503+131T>A MANE Plus Clinical	NP_001006658.1:n.1503+131T>A
NM_020779.4:c.1470+131T>A MANE Select	NP_065830.2:n.1470+131T>A