Canonical Allele Identifier: CA2243000555

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728589T= , CM000679.2:g.1728589T=	GRCh38
NC_000017.10:g.1631883T= , CM000679.1:g.1631883T=	GRCh37
NC_000017.9:g.1578633T=	NCBI36
NG_032811.1:g.17067T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3630T= MANE Select	ENSP00000386609.1:p.Pro1210=
ENST00000309182.9:c.477T=	ENSP00000312074.5:p.Pro159=
ENST00000409644.5:c.3630T=	ENSP00000386609.1:p.Pro1210=
ENST00000418841.5:c.-88-3736T=	ENSP00000395198.1:n.-88-3736T=
ENST00000419248.5:c.-14-1791T=	ENSP00000407845.1:n.-14-1791T=
ENST00000437219.6:c.59-1791T=	ENSP00000391074.2:n.59-1791T=
ENST00000446363.5:c.-308-2166T=	ENSP00000401560.1:n.-308-2166T=
ENST00000455636.5:c.59-1791T=	ENSP00000395226.1:n.59-1791T=
ENST00000464528.5:n.1016T=
ENST00000468539.5:c.63-3736T=	ENSP00000460742.1:n.63-3736T=
ENST00000492901.1:n.88-1791T=
ENST00000575206.1:c.380T=
NM_001163673.1:c.59-1791T=	NP_001157145.1:n.59-1791T=
NM_001163809.1:c.3630T=	NP_001157281.1:p.Pro1210=
NM_001163811.1:c.-14-1791T=	NP_001157283.1:n.-14-1791T=
NM_152348.3:c.477T=	NP_689561.2:p.Pro159=
XM_005256454.2:c.3630T=	XP_005256511.1:p.Pro1210=
XM_011523650.1:c.3630T=	XP_011521952.1:p.Pro1210=
XM_011523651.1:c.477T=	XP_011521953.1:p.Pro159=
XR_933973.1:n.3774T=
XM_011523651.2:c.477T=	XP_011521953.1:p.Pro159=
XM_017024184.1:c.3630T=	XP_016879673.1:p.Pro1210=
XR_001752427.1:n.3782T=
XR_933973.2:n.3782T=
NM_001163809.2:c.3630T= MANE Select	NP_001157281.1:p.Pro1210=
NM_001163811.2:c.-14-1791T=	NP_001157283.1:n.-14-1791T=
NM_152348.4:c.477T=	NP_689561.2:p.Pro159=
NM_001163673.2:c.59-1791T=	NP_001157145.1:n.59-1791T=