Canonical Allele Identifier: CA1557012052

Gene: WDR41

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.77447656A= , CM000667.2:g.77447656A=	GRCh38
NC_000005.9:g.76743481A= , CM000667.1:g.76743481A=	GRCh37
NC_000005.8:g.76779237A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018268.4:c.697+2104T= MANE Select	NP_060738.2:n.697+2104T=
ENST00000296679.9:c.697+2104T= MANE Select	ENSP00000296679.4:n.697+2104T=
NM_018268.2:c.697+2104T=	NP_060738.2:n.697+2104T=
NM_018268.3:c.697+2104T=	NP_060738.2:n.697+2104T=
ENST00000296679.8:c.697+2104T=	ENSP00000296679.4:n.697+2104T=
ENST00000414719.6:c.*111+2104T=	ENSP00000392931.3:n.*111+2104T=
ENST00000502528.5:n.1694+2104T=
ENST00000505129.5:c.*111+2104T=	ENSP00000425249.1:n.*111+2104T=
ENST00000506307.5:c.*56+2104T=	ENSP00000424327.1:n.*56+2104T=
ENST00000507029.5:c.532+2104T=	ENSP00000424287.1:n.532+2104T=
ENST00000507654.5:c.11-6659T=	ENSP00000427291.1:n.11-6659T=
ENST00000509701.5:c.624+2104T=	ENSP00000427652.1:n.624+2104T=
ENST00000511630.6:c.174+2104T=
ENST00000511791.1:c.74-6659T=	ENSP00000423540.1:n.74-6659T=
ENST00000515253.5:c.502+6161T=	ENSP00000426499.1:n.502+6161T=
XM_005248551.3:c.523+6161T=	XP_005248608.1:n.523+6161T=
XM_005248551.4:c.523+6161T=	XP_005248608.1:n.523+6161T=
XM_005248552.2:c.697+2104T=	XP_005248609.1:n.697+2104T=
XM_005248552.3:c.697+2104T=	XP_005248609.1:n.697+2104T=
XM_006714656.2:c.697+2104T=	XP_006714719.1:n.697+2104T=
XM_011543505.1:c.688+2104T=	XP_011541807.1:n.688+2104T=
XM_011543505.2:c.688+2104T=	XP_011541807.1:n.688+2104T=
XM_011543506.1:c.541+2104T=	XP_011541808.1:n.541+2104T=
XM_011543507.1:c.697+2104T=	XP_011541809.1:n.697+2104T=
XM_011543507.2:c.697+2104T=	XP_011541809.1:n.697+2104T=
XM_017009606.1:c.685+2104T=	XP_016865095.1:n.685+2104T=
XR_001742140.1:n.984+2104T=
XR_001742141.1:n.984+2104T=