Canonical Allele Identifier: CA10045814

Gene: WDR4

Linked Data

• ClinVar Variation Id: 2051888
• ClinVar RCV Id: RCV002927598
• dbSNP Id: rs773296163
• ExAC: 21:44270370 G / A
• gnomAD v2: 21-44270370-G-A
• gnomAD v3: 21-42850260-G-A
• gnomAD v4: 21-42850260-G-A
• MyVariant Identifiers: chr21:g.44270370G>A (hg19) ; chr21:g.42850260G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42850260G>A , CM000683.2:g.42850260G>A	GRCh38
NC_000021.8:g.44270370G>A , CM000683.1:g.44270370G>A	GRCh37
NC_000021.7:g.43143439G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398208.3:c.1046-18C>T MANE Select	ENSP00000381266.2:n.1046-18C>T
ENST00000330317.6:c.1046-18C>T	ENSP00000328671.2:n.1046-18C>T
ENST00000398208.2:c.1046-18C>T	ENSP00000381266.2:n.1046-18C>T
ENST00000476326.5:n.961-18C>T
ENST00000492742.5:n.1189-18C>T
NM_001260474.1:c.1043-18C>T	NP_001247403.1:n.1043-18C>T
NM_001260475.1:c.608-18C>T	NP_001247404.1:n.608-18C>T
NM_001260476.1:c.608-18C>T	NP_001247405.1:n.608-18C>T
NM_001260477.1:c.608-18C>T	NP_001247406.1:n.608-18C>T
NM_018669.5:c.1046-18C>T	NP_061139.2:n.1046-18C>T
NM_033661.4:c.1046-18C>T	NP_387510.1:n.1046-18C>T
NR_048535.1:n.1026-18C>T
XM_011529433.1:c.1034-18C>T	XP_011527735.1:n.1034-18C>T
XR_937429.1:n.1120-18C>T
XR_937430.1:n.1120-18C>T
XR_937431.1:n.1120-18C>T
XM_017028262.1:c.941-18C>T	XP_016883751.1:n.941-18C>T
XM_017028263.1:c.776-18C>T	XP_016883752.1:n.776-18C>T
XM_017028264.1:c.776-18C>T	XP_016883753.1:n.776-18C>T
XM_024452047.1:c.608-18C>T	XP_024307815.1:n.608-18C>T
XM_024452048.1:c.608-18C>T	XP_024307816.1:n.608-18C>T
XM_024452049.1:c.608-18C>T	XP_024307817.1:n.608-18C>T
XM_024452050.1:c.608-18C>T	XP_024307818.1:n.608-18C>T
NM_018669.6:c.1046-18C>T MANE Select	NP_061139.2:n.1046-18C>T
NM_001260474.2:c.1043-18C>T	NP_001247403.1:n.1043-18C>T
NM_001260475.2:c.608-18C>T	NP_001247404.1:n.608-18C>T
NM_001260476.2:c.608-18C>T	NP_001247405.1:n.608-18C>T
NM_001260477.2:c.608-18C>T	NP_001247406.1:n.608-18C>T
NM_033661.5:c.1046-18C>T	NP_387510.1:n.1046-18C>T