Canonical Allele Identifier: CA410392508

Gene: WDR4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42862339C>T , CM000683.2:g.42862339C>T	GRCh38
NC_000021.8:g.44282449C>T , CM000683.1:g.44282449C>T	GRCh37
NC_000021.7:g.43155518C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018669.6:c.509G>A MANE Select	NP_061139.2:p.Arg170Gln
ENST00000398208.3:c.509G>A MANE Select	ENSP00000381266.2:p.Arg170Gln
NM_001260474.1:c.509G>A	NP_001247403.1:p.Arg170Gln
NM_001260474.2:c.509G>A	NP_001247403.1:p.Arg170Gln
NM_001260475.1:c.71G>A	NP_001247404.1:p.Arg24Gln
NM_001260475.2:c.71G>A	NP_001247404.1:p.Arg24Gln
NM_001260476.1:c.71G>A	NP_001247405.1:p.Arg24Gln
NM_001260476.2:c.71G>A	NP_001247405.1:p.Arg24Gln
NM_001260477.1:c.71G>A	NP_001247406.1:p.Arg24Gln
NM_001260477.2:c.71G>A	NP_001247406.1:p.Arg24Gln
NM_018669.5:c.509G>A	NP_061139.2:p.Arg170Gln
NM_033661.4:c.509G>A	NP_387510.1:p.Arg170Gln
NM_033661.5:c.509G>A	NP_387510.1:p.Arg170Gln
NR_048535.1:n.489G>A
ENST00000330317.6:c.509G>A	ENSP00000328671.2:p.Arg170Gln
ENST00000398208.2:c.509G>A	ENSP00000381266.2:p.Arg170Gln
ENST00000463902.5:n.394G>A
ENST00000470658.1:n.844G>A
ENST00000476326.5:n.424G>A
ENST00000479429.5:n.477G>A
ENST00000492742.5:n.652G>A
XM_011529433.1:c.497G>A	XP_011527735.1:p.Arg166Gln
XM_017028262.1:c.462-2617G>A	XP_016883751.1:n.462-2617G>A
XM_017028263.1:c.297-2617G>A	XP_016883752.1:n.297-2617G>A
XM_017028264.1:c.297-2617G>A	XP_016883753.1:n.297-2617G>A
XM_024452047.1:c.71G>A	XP_024307815.1:p.Arg24Gln
XM_024452048.1:c.71G>A	XP_024307816.1:p.Arg24Gln
XM_024452049.1:c.71G>A	XP_024307817.1:p.Arg24Gln
XM_024452050.1:c.71G>A	XP_024307818.1:p.Arg24Gln
XR_937429.1:n.583G>A
XR_937430.1:n.583G>A
XR_937431.1:n.583G>A