Canonical Allele Identifier: CA2576684483

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989227_19989230dup , CM000664.2:g.19989227_19989230dup	GRCh38
NC_000002.11:g.20188988_20188991dup , CM000664.1:g.20188988_20188991dup	GRCh37
NC_000002.10:g.20052469_20052472dup	NCBI36
NG_021212.1:g.5894_5897dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.77_80dup MANE Select	ENSP00000281405.5:p.Phe28ArgfsTer8
ENST00000345530.8:c.77_80dup MANE Plus Clinical	ENSP00000314444.5:p.Phe28ArgfsTer8
ENST00000281405.8:c.77_80dup	ENSP00000281405.4:p.Phe28ArgfsTer8
ENST00000345530.7:c.77_80dup	ENSP00000314444.5:p.Phe28ArgfsTer8
ENST00000414212.5:c.77_80dup	ENSP00000390802.1:p.Phe28ArgfsTer8
NM_001006657.1:c.77_80dup	NP_001006658.1:p.Phe28ArgfsTer8
NM_020779.3:c.77_80dup	NP_065830.2:p.Phe28ArgfsTer8
XR_426989.2:n.110_113dup
XR_939699.1:n.110_113dup
XR_001738862.1:n.110_113dup
XR_426989.3:n.110_113dup
XR_939699.3:n.110_113dup
NM_001006657.2:c.77_80dup MANE Plus Clinical	NP_001006658.1:p.Phe28ArgfsTer8
NM_020779.4:c.77_80dup MANE Select	NP_065830.2:p.Phe28ArgfsTer8