Canonical Allele Identifier: CA2242999682

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728170G= , CM000679.2:g.1728170G=	GRCh38
NC_000017.10:g.1631464G= , CM000679.1:g.1631464G=	GRCh37
NC_000017.9:g.1578214G=	NCBI36
NG_032811.1:g.16648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3211G= MANE Select	ENSP00000386609.1:p.Val1071=
ENST00000309182.9:c.58G=	ENSP00000312074.5:p.Val20=
ENST00000409644.5:c.3211G=	ENSP00000386609.1:p.Val1071=
ENST00000418841.5:c.-89+3384G=	ENSP00000395198.1:n.-89+3384G=
ENST00000419248.5:c.-14-2210G=	ENSP00000407845.1:n.-14-2210G=
ENST00000437219.6:c.59-2210G=	ENSP00000391074.2:n.59-2210G=
ENST00000446363.5:c.-308-2585G=	ENSP00000401560.1:n.-308-2585G=
ENST00000455636.5:c.59-2210G=	ENSP00000395226.1:n.59-2210G=
ENST00000464528.5:n.597G=
ENST00000468539.5:c.63-4155G=	ENSP00000460742.1:n.63-4155G=
ENST00000492901.1:n.88-2210G=
NM_001163673.1:c.59-2210G=	NP_001157145.1:n.59-2210G=
NM_001163809.1:c.3211G=	NP_001157281.1:p.Val1071=
NM_001163811.1:c.-14-2210G=	NP_001157283.1:n.-14-2210G=
NM_152348.3:c.58G=	NP_689561.2:p.Val20=
XM_005256454.2:c.3211G=	XP_005256511.1:p.Val1071=
XM_011523650.1:c.3211G=	XP_011521952.1:p.Val1071=
XM_011523651.1:c.58G=	XP_011521953.1:p.Val20=
XR_933973.1:n.3355G=
XM_011523651.2:c.58G=	XP_011521953.1:p.Val20=
XM_017024184.1:c.3211G=	XP_016879673.1:p.Val1071=
XR_001752427.1:n.3363G=
XR_933973.2:n.3363G=
NM_001163809.2:c.3211G= MANE Select	NP_001157281.1:p.Val1071=
NM_001163811.2:c.-14-2210G=	NP_001157283.1:n.-14-2210G=
NM_152348.4:c.58G=	NP_689561.2:p.Val20=
NM_001163673.2:c.59-2210G=	NP_001157145.1:n.59-2210G=