Canonical Allele Identifier: CA2749073862

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989367_19989368insAGA , CM000664.2:g.19989367_19989368insAGA	GRCh38
NC_000002.11:g.20189128_20189129insAGA , CM000664.1:g.20189128_20189129insAGA	GRCh37
NC_000002.10:g.20052609_20052610insAGA	NCBI36
NG_021212.1:g.5756_5757insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.25-86_25-85insTCT MANE Select	ENSP00000281405.5:n.25-86_25-85insTCT
ENST00000345530.8:c.25-86_25-85insTCT MANE Plus Clinical	ENSP00000314444.5:n.25-86_25-85insTCT
ENST00000281405.8:c.25-86_25-85insTCT	ENSP00000281405.4:n.25-86_25-85insTCT
ENST00000345530.7:c.25-86_25-85insTCT	ENSP00000314444.5:n.25-86_25-85insTCT
ENST00000414212.5:c.25-86_25-85insTCT	ENSP00000390802.1:n.25-86_25-85insTCT
NM_001006657.1:c.25-86_25-85insTCT	NP_001006658.1:n.25-86_25-85insTCT
NM_020779.3:c.25-86_25-85insTCT	NP_065830.2:n.25-86_25-85insTCT
XR_426989.2:n.58-86_58-85insTCT
XR_939699.1:n.58-86_58-85insTCT
XR_001738862.1:n.58-86_58-85insTCT
XR_426989.3:n.58-86_58-85insTCT
XR_939699.3:n.58-86_58-85insTCT
NM_001006657.2:c.25-86_25-85insTCT MANE Plus Clinical	NP_001006658.1:n.25-86_25-85insTCT
NM_020779.4:c.25-86_25-85insTCT MANE Select	NP_065830.2:n.25-86_25-85insTCT