Canonical Allele Identifier: CA2243010627

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1731098C= , CM000679.2:g.1731098C=	GRCh38
NC_000017.10:g.1634392C= , CM000679.1:g.1634392C=	GRCh37
NC_000017.9:g.1581142C=	NCBI36
NG_032811.1:g.19576C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001163809.2:c.3997C= MANE Select	NP_001157281.1:p.Arg1333=
ENST00000409644.6:c.3997C= MANE Select	ENSP00000386609.1:p.Arg1333=
NM_001163673.1:c.388C=	NP_001157145.1:p.Arg130=
NM_001163673.2:c.388C=	NP_001157145.1:p.Arg130=
NM_001163809.1:c.3997C=	NP_001157281.1:p.Arg1333=
NM_001163811.1:c.316C=	NP_001157283.1:p.Arg106=
NM_001163811.2:c.316C=	NP_001157283.1:p.Arg106=
NM_152348.3:c.844C=	NP_689561.2:p.Arg282=
NM_152348.4:c.844C=	NP_689561.2:p.Arg282=
ENST00000309182.9:c.844C=	ENSP00000312074.5:p.Arg282=
ENST00000409644.5:c.3997C=	ENSP00000386609.1:p.Arg1333=
ENST00000418841.5:c.-88-1227C=	ENSP00000395198.1:n.-88-1227C=
ENST00000419248.5:c.316C=	ENSP00000407845.1:p.Arg106=
ENST00000437219.6:c.388C=	ENSP00000391074.2:p.Arg130=
ENST00000446363.5:c.-87C=	ENSP00000401560.1:n.-87C=
ENST00000455636.5:c.388C=	ENSP00000395226.1:p.Arg130=
ENST00000464528.5:n.1383C=
ENST00000468539.5:c.63-1227C=	ENSP00000460742.1:n.63-1227C=
ENST00000474958.2:c.218+153C=
ENST00000479966.1:n.506C=
XM_005256454.2:c.3997C=	XP_005256511.1:p.Arg1333=
XM_011523650.1:c.3997C=	XP_011521952.1:p.Arg1333=
XM_011523651.1:c.844C=	XP_011521953.1:p.Arg282=
XM_011523651.2:c.844C=	XP_011521953.1:p.Arg282=
XM_017024184.1:c.3997C=	XP_016879673.1:p.Arg1333=
XR_001752427.1:n.4149C=
XR_933973.1:n.4141C=
XR_933973.2:n.4149C=