Canonical Allele Identifier: CA1543311
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 288323
dbSNP Id: rs142103808
gnomAD v2: 2-20162080-G-A
gnomAD v3: 2-19962319-G-A
gnomAD v4: 2-19962319-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19962319G>A , CM000664.2:g.19962319G>A GRCh38
NC_000002.11:g.20162080G>A , CM000664.1:g.20162080G>A GRCh37
NC_000002.10:g.20025561G>A NCBI36
NG_021212.1:g.32805C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.1195-1705C>T MANE Select ENSP00000281405.5:n.1195-1705C>T
ENST00000345530.8:c.1203C>T MANE Plus Clinical ENSP00000314444.5:p.Asn401=
ENST00000281405.8:c.1195-1705C>T ENSP00000281405.4:n.1195-1705C>T
ENST00000345530.7:c.1203C>T ENSP00000314444.5:p.Asn401=
ENST00000414212.5:c.1203C>T ENSP00000390802.1:p.Asn401=
ENST00000445063.5:c.731+4405C>T
NM_001006657.1:c.1203C>T NP_001006658.1:p.Asn401=
NM_020779.3:c.1195-1705C>T NP_065830.2:n.1195-1705C>T
XM_011533007.1:c.-18+4405C>T XP_011531309.1:n.-18+4405C>T
XR_426989.2:n.1228-1705C>T
XR_939699.1:n.1228-1705C>T
XM_011533007.2:c.-18+4405C>T XP_011531309.1:n.-18+4405C>T
XR_001738862.1:n.1228-1705C>T
XR_426989.3:n.1228-1705C>T
XR_939699.3:n.1228-1705C>T
NM_001006657.2:c.1203C>T MANE Plus Clinical NP_001006658.1:p.Asn401=
NM_020779.4:c.1195-1705C>T MANE Select NP_065830.2:n.1195-1705C>T