Canonical Allele Identifier: CA10046209

Gene: WDR4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42873581C>T , CM000683.2:g.42873581C>T	GRCh38
NC_000021.8:g.44293691C>T , CM000683.1:g.44293691C>T	GRCh37
NC_000021.7:g.43166760C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018669.6:c.266G>A MANE Select	NP_061139.2:p.Arg89His
ENST00000398208.3:c.266G>A MANE Select	ENSP00000381266.2:p.Arg89His
NM_001260474.1:c.266G>A	NP_001247403.1:p.Arg89His
NM_001260474.2:c.266G>A	NP_001247403.1:p.Arg89His
NM_001260475.1:c.-143+22G>A	NP_001247404.1:n.-143+22G>A
NM_001260475.2:c.-143+22G>A	NP_001247404.1:n.-143+22G>A
NM_001260476.1:c.-143+22G>A	NP_001247405.1:n.-143+22G>A
NM_001260476.2:c.-143+22G>A	NP_001247405.1:n.-143+22G>A
NM_001260477.1:c.-143+22G>A	NP_001247406.1:n.-143+22G>A
NM_001260477.2:c.-143+22G>A	NP_001247406.1:n.-143+22G>A
NM_018669.5:c.266G>A	NP_061139.2:p.Arg89His
NM_033661.4:c.266G>A	NP_387510.1:p.Arg89His
NM_033661.5:c.266G>A	NP_387510.1:p.Arg89His
NR_048535.1:n.246G>A
ENST00000330317.6:c.266G>A	ENSP00000328671.2:p.Arg89His
ENST00000398208.2:c.266G>A	ENSP00000381266.2:p.Arg89His
ENST00000463902.5:n.181+22G>A
ENST00000470658.1:n.601G>A
ENST00000476326.5:n.211+22G>A
ENST00000479429.5:n.264+22G>A
ENST00000492742.5:n.439+22G>A
XM_011529433.1:c.254G>A	XP_011527735.1:p.Arg85His
XM_017028262.1:c.431G>A	XP_016883751.1:p.Arg144His
XM_017028263.1:c.266G>A	XP_016883752.1:p.Arg89His
XM_017028264.1:c.266G>A	XP_016883753.1:p.Arg89His
XM_024452047.1:c.-173G>A	XP_024307815.1:n.-173G>A
XM_024452048.1:c.-173G>A	XP_024307816.1:n.-173G>A
XM_024452049.1:c.-143+22G>A	XP_024307817.1:n.-143+22G>A
XM_024452050.1:c.-173G>A	XP_024307818.1:n.-173G>A
XR_937429.1:n.340G>A
XR_937430.1:n.340G>A
XR_937431.1:n.340G>A