Canonical Allele Identifier: CA410393329

Gene: WDR4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42862396T>G , CM000683.2:g.42862396T>G	GRCh38
NC_000021.8:g.44282506T>G , CM000683.1:g.44282506T>G	GRCh37
NC_000021.7:g.43155575T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018669.6:c.454-2A>C MANE Select	NP_061139.2:n.454-2A>C
ENST00000398208.3:c.454-2A>C MANE Select	ENSP00000381266.2:n.454-2A>C
NM_001260474.1:c.454-2A>C	NP_001247403.1:n.454-2A>C
NM_001260474.2:c.454-2A>C	NP_001247403.1:n.454-2A>C
NM_001260475.1:c.16-2A>C	NP_001247404.1:n.16-2A>C
NM_001260475.2:c.16-2A>C	NP_001247404.1:n.16-2A>C
NM_001260476.1:c.16-2A>C	NP_001247405.1:n.16-2A>C
NM_001260476.2:c.16-2A>C	NP_001247405.1:n.16-2A>C
NM_001260477.1:c.16-2A>C	NP_001247406.1:n.16-2A>C
NM_001260477.2:c.16-2A>C	NP_001247406.1:n.16-2A>C
NM_018669.5:c.454-2A>C	NP_061139.2:n.454-2A>C
NM_033661.4:c.454-2A>C	NP_387510.1:n.454-2A>C
NM_033661.5:c.454-2A>C	NP_387510.1:n.454-2A>C
NR_048535.1:n.434-2A>C
ENST00000330317.6:c.454-2A>C	ENSP00000328671.2:n.454-2A>C
ENST00000398208.2:c.454-2A>C	ENSP00000381266.2:n.454-2A>C
ENST00000463902.5:n.339-2A>C
ENST00000470658.1:n.789-2A>C
ENST00000476326.5:n.369-2A>C
ENST00000479429.5:n.422-2A>C
ENST00000492742.5:n.597-2A>C
XM_011529433.1:c.442-2A>C	XP_011527735.1:n.442-2A>C
XM_017028262.1:c.462-2674A>C	XP_016883751.1:n.462-2674A>C
XM_017028263.1:c.297-2674A>C	XP_016883752.1:n.297-2674A>C
XM_017028264.1:c.297-2674A>C	XP_016883753.1:n.297-2674A>C
XM_024452047.1:c.16-2A>C	XP_024307815.1:n.16-2A>C
XM_024452048.1:c.16-2A>C	XP_024307816.1:n.16-2A>C
XM_024452049.1:c.16-2A>C	XP_024307817.1:n.16-2A>C
XM_024452050.1:c.16-2A>C	XP_024307818.1:n.16-2A>C
XR_937429.1:n.528-2A>C
XR_937430.1:n.528-2A>C
XR_937431.1:n.528-2A>C