Canonical Allele Identifier: CA2499215560

Gene: WDR35

Linked Data

• ClinVar Variation Id: 1072199
• ClinVar RCV Id: RCV001384852
• dbSNP Id: rs2103399754

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19933421dup , CM000664.2:g.19933421dup	GRCh38
NC_000002.11:g.20133182dup , CM000664.1:g.20133182dup	GRCh37
NC_000002.10:g.19996663dup	NCBI36
NG_021212.1:g.61703dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.2638dup MANE Select	ENSP00000281405.5:p.Thr880AsnfsTer13
ENST00000345530.8:c.2671dup MANE Plus Clinical	ENSP00000314444.5:p.Thr891AsnfsTer13
ENST00000281405.8:c.2638dup	ENSP00000281405.4:p.Thr880AsnfsTer13
ENST00000345530.7:c.2671dup	ENSP00000314444.5:p.Thr891AsnfsTer13
ENST00000414212.5:c.*53dup	ENSP00000390802.1:n.*53dup
ENST00000445063.5:c.2024-2012dup
NM_001006657.1:c.2671dup	NP_001006658.1:p.Thr891AsnfsTer13
NM_020779.3:c.2638dup	NP_065830.2:p.Thr880AsnfsTer13
XM_011533007.1:c.1366dup	XP_011531309.1:p.Thr456AsnfsTer13
XR_426989.2:n.2671dup
XM_011533007.2:c.1366dup	XP_011531309.1:p.Thr456AsnfsTer13
XR_001738862.1:n.2615dup
XR_426989.3:n.2671dup
NM_001006657.2:c.2671dup MANE Plus Clinical	NP_001006658.1:p.Thr891AsnfsTer13
NM_020779.4:c.2638dup MANE Select	NP_065830.2:p.Thr880AsnfsTer13