Canonical Allele Identifier: CA10045809
Gene: WDR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044965
ClinVar RCV Id: RCV002917820
dbSNP Id: rs766918418

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42850243C>T , CM000683.2:g.42850243C>T GRCh38
NC_000021.8:g.44270353C>T , CM000683.1:g.44270353C>T GRCh37
NC_000021.7:g.43143422C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398208.3:c.1046-1G>A MANE Select ENSP00000381266.2:n.1046-1G>A
ENST00000330317.6:c.1046-1G>A ENSP00000328671.2:n.1046-1G>A
ENST00000398208.2:c.1046-1G>A ENSP00000381266.2:n.1046-1G>A
ENST00000476326.5:n.961-1G>A
ENST00000492742.5:n.1189-1G>A
NM_001260474.1:c.1043-1G>A NP_001247403.1:n.1043-1G>A
NM_001260475.1:c.608-1G>A NP_001247404.1:n.608-1G>A
NM_001260476.1:c.608-1G>A NP_001247405.1:n.608-1G>A
NM_001260477.1:c.608-1G>A NP_001247406.1:n.608-1G>A
NM_018669.5:c.1046-1G>A NP_061139.2:n.1046-1G>A
NM_033661.4:c.1046-1G>A NP_387510.1:n.1046-1G>A
NR_048535.1:n.1026-1G>A
XM_011529433.1:c.1034-1G>A XP_011527735.1:n.1034-1G>A
XR_937429.1:n.1120-1G>A
XR_937430.1:n.1120-1G>A
XR_937431.1:n.1120-1G>A
XM_017028262.1:c.941-1G>A XP_016883751.1:n.941-1G>A
XM_017028263.1:c.776-1G>A XP_016883752.1:n.776-1G>A
XM_017028264.1:c.776-1G>A XP_016883753.1:n.776-1G>A
XM_024452047.1:c.608-1G>A XP_024307815.1:n.608-1G>A
XM_024452048.1:c.608-1G>A XP_024307816.1:n.608-1G>A
XM_024452049.1:c.608-1G>A XP_024307817.1:n.608-1G>A
XM_024452050.1:c.608-1G>A XP_024307818.1:n.608-1G>A
NM_018669.6:c.1046-1G>A MANE Select NP_061139.2:n.1046-1G>A
NM_001260474.2:c.1043-1G>A NP_001247403.1:n.1043-1G>A
NM_001260475.2:c.608-1G>A NP_001247404.1:n.608-1G>A
NM_001260476.2:c.608-1G>A NP_001247405.1:n.608-1G>A
NM_001260477.2:c.608-1G>A NP_001247406.1:n.608-1G>A
NM_033661.5:c.1046-1G>A NP_387510.1:n.1046-1G>A