Canonical Allele Identifier: CA2749073856

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989361_19989362insACAG , CM000664.2:g.19989361_19989362insACAG	GRCh38
NC_000002.11:g.20189122_20189123insACAG , CM000664.1:g.20189122_20189123insACAG	GRCh37
NC_000002.10:g.20052603_20052604insACAG	NCBI36
NG_021212.1:g.5762_5763insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.25-80_25-79insCTGT MANE Select	ENSP00000281405.5:n.25-80_25-79insCTGT
ENST00000345530.8:c.25-80_25-79insCTGT MANE Plus Clinical	ENSP00000314444.5:n.25-80_25-79insCTGT
ENST00000281405.8:c.25-80_25-79insCTGT	ENSP00000281405.4:n.25-80_25-79insCTGT
ENST00000345530.7:c.25-80_25-79insCTGT	ENSP00000314444.5:n.25-80_25-79insCTGT
ENST00000414212.5:c.25-80_25-79insCTGT	ENSP00000390802.1:n.25-80_25-79insCTGT
NM_001006657.1:c.25-80_25-79insCTGT	NP_001006658.1:n.25-80_25-79insCTGT
NM_020779.3:c.25-80_25-79insCTGT	NP_065830.2:n.25-80_25-79insCTGT
XR_426989.2:n.58-80_58-79insCTGT
XR_939699.1:n.58-80_58-79insCTGT
XR_001738862.1:n.58-80_58-79insCTGT
XR_426989.3:n.58-80_58-79insCTGT
XR_939699.3:n.58-80_58-79insCTGT
NM_001006657.2:c.25-80_25-79insCTGT MANE Plus Clinical	NP_001006658.1:n.25-80_25-79insCTGT
NM_020779.4:c.25-80_25-79insCTGT MANE Select	NP_065830.2:n.25-80_25-79insCTGT