Canonical Allele Identifier: CA763233592

Gene: WDR35

Linked Data

• dbSNP Id: rs1473263220
• gnomAD v3: 2-19989332-GAAGT-G
• gnomAD v4: 2-19989332-GAAGT-G
• MyVariant Identifiers: chr2:g.20189094_20189097del (hg19) ; chr2:g.19989333_19989336del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989337_19989340del , CM000664.2:g.19989337_19989340del	GRCh38
NC_000002.11:g.20189098_20189101del , CM000664.1:g.20189098_20189101del	GRCh37
NC_000002.10:g.20052579_20052582del	NCBI36
NG_021212.1:g.5788_5791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.25-54_25-51del MANE Select	ENSP00000281405.5:n.25-54_25-51del
ENST00000345530.8:c.25-54_25-51del MANE Plus Clinical	ENSP00000314444.5:n.25-54_25-51del
ENST00000281405.8:c.25-54_25-51del	ENSP00000281405.4:n.25-54_25-51del
ENST00000345530.7:c.25-54_25-51del	ENSP00000314444.5:n.25-54_25-51del
ENST00000414212.5:c.25-54_25-51del	ENSP00000390802.1:n.25-54_25-51del
NM_001006657.1:c.25-54_25-51del	NP_001006658.1:n.25-54_25-51del
NM_020779.3:c.25-54_25-51del	NP_065830.2:n.25-54_25-51del
XR_426989.2:n.58-54_58-51del
XR_939699.1:n.58-54_58-51del
XR_001738862.1:n.58-54_58-51del
XR_426989.3:n.58-54_58-51del
XR_939699.3:n.58-54_58-51del
NM_001006657.2:c.25-54_25-51del MANE Plus Clinical	NP_001006658.1:n.25-54_25-51del
NM_020779.4:c.25-54_25-51del MANE Select	NP_065830.2:n.25-54_25-51del