Canonical Allele Identifier: CA2242999969

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728323G= , CM000679.2:g.1728323G=	GRCh38
NC_000017.10:g.1631617G= , CM000679.1:g.1631617G=	GRCh37
NC_000017.9:g.1578367G=	NCBI36
NG_032811.1:g.16801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3364G= MANE Select	ENSP00000386609.1:p.Glu1122=
ENST00000309182.9:c.211G=	ENSP00000312074.5:p.Glu71=
ENST00000409644.5:c.3364G=	ENSP00000386609.1:p.Glu1122=
ENST00000418841.5:c.-89+3537G=	ENSP00000395198.1:n.-89+3537G=
ENST00000419248.5:c.-14-2057G=	ENSP00000407845.1:n.-14-2057G=
ENST00000437219.6:c.59-2057G=	ENSP00000391074.2:n.59-2057G=
ENST00000446363.5:c.-308-2432G=	ENSP00000401560.1:n.-308-2432G=
ENST00000455636.5:c.59-2057G=	ENSP00000395226.1:n.59-2057G=
ENST00000464528.5:n.750G=
ENST00000468539.5:c.63-4002G=	ENSP00000460742.1:n.63-4002G=
ENST00000492901.1:n.88-2057G=
ENST00000575206.1:c.114G=
NM_001163673.1:c.59-2057G=	NP_001157145.1:n.59-2057G=
NM_001163809.1:c.3364G=	NP_001157281.1:p.Glu1122=
NM_001163811.1:c.-14-2057G=	NP_001157283.1:n.-14-2057G=
NM_152348.3:c.211G=	NP_689561.2:p.Glu71=
XM_005256454.2:c.3364G=	XP_005256511.1:p.Glu1122=
XM_011523650.1:c.3364G=	XP_011521952.1:p.Glu1122=
XM_011523651.1:c.211G=	XP_011521953.1:p.Glu71=
XR_933973.1:n.3508G=
XM_011523651.2:c.211G=	XP_011521953.1:p.Glu71=
XM_017024184.1:c.3364G=	XP_016879673.1:p.Glu1122=
XR_001752427.1:n.3516G=
XR_933973.2:n.3516G=
NM_001163809.2:c.3364G= MANE Select	NP_001157281.1:p.Glu1122=
NM_001163811.2:c.-14-2057G=	NP_001157283.1:n.-14-2057G=
NM_152348.4:c.211G=	NP_689561.2:p.Glu71=
NM_001163673.2:c.59-2057G=	NP_001157145.1:n.59-2057G=