Canonical Allele Identifier: CA2749073793

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989005_19989113del , CM000664.2:g.19989005_19989113del	GRCh38
NC_000002.11:g.20188766_20188874del , CM000664.1:g.20188766_20188874del	GRCh37
NC_000002.10:g.20052247_20052355del	NCBI36
NG_021212.1:g.6017_6125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.142+58_142+166del MANE Select	ENSP00000281405.5:n.142+58_142+166del
ENST00000345530.8:c.142+58_142+166del MANE Plus Clinical	ENSP00000314444.5:n.142+58_142+166del
ENST00000281405.8:c.142+58_142+166del	ENSP00000281405.4:n.142+58_142+166del
ENST00000345530.7:c.142+58_142+166del	ENSP00000314444.5:n.142+58_142+166del
ENST00000414212.5:c.142+58_142+166del	ENSP00000390802.1:n.142+58_142+166del
NM_001006657.1:c.142+58_142+166del	NP_001006658.1:n.142+58_142+166del
NM_020779.3:c.142+58_142+166del	NP_065830.2:n.142+58_142+166del
XR_426989.2:n.175+58_175+166del
XR_939699.1:n.175+58_175+166del
XR_001738862.1:n.175+58_175+166del
XR_426989.3:n.175+58_175+166del
XR_939699.3:n.175+58_175+166del
NM_001006657.2:c.142+58_142+166del MANE Plus Clinical	NP_001006658.1:n.142+58_142+166del
NM_020779.4:c.142+58_142+166del MANE Select	NP_065830.2:n.142+58_142+166del