Canonical Allele Identifier: CA2576684486
Gene: WDR35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19989342T>A , CM000664.2:g.19989342T>A GRCh38
NC_000002.11:g.20189103T>A , CM000664.1:g.20189103T>A GRCh37
NC_000002.10:g.20052584T>A NCBI36
NG_021212.1:g.5782A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.25-60A>T MANE Select ENSP00000281405.5:n.25-60A>T
ENST00000345530.8:c.25-60A>T MANE Plus Clinical ENSP00000314444.5:n.25-60A>T
ENST00000281405.8:c.25-60A>T ENSP00000281405.4:n.25-60A>T
ENST00000345530.7:c.25-60A>T ENSP00000314444.5:n.25-60A>T
ENST00000414212.5:c.25-60A>T ENSP00000390802.1:n.25-60A>T
NM_001006657.1:c.25-60A>T NP_001006658.1:n.25-60A>T
NM_020779.3:c.25-60A>T NP_065830.2:n.25-60A>T
XR_426989.2:n.58-60A>T
XR_939699.1:n.58-60A>T
XR_001738862.1:n.58-60A>T
XR_426989.3:n.58-60A>T
XR_939699.3:n.58-60A>T
NM_001006657.2:c.25-60A>T MANE Plus Clinical NP_001006658.1:n.25-60A>T
NM_020779.4:c.25-60A>T MANE Select NP_065830.2:n.25-60A>T