Canonical Allele Identifier: CA2333968533

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36097074C= , CM000681.2:g.36097074C=	GRCh38
NC_000019.9:g.36587976C= , CM000681.1:g.36587976C=	GRCh37
NC_000019.8:g.41279816C=	NCBI36
NG_028101.1:g.47194C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001083961.2:c.2515C= MANE Select	NP_001077430.1:p.Arg839=
ENST00000401500.7:c.2515C= MANE Select	ENSP00000384792.1:p.Arg839=
NM_001083961.1:c.2515C=	NP_001077430.1:p.Arg839=
NM_173636.4:c.2515C=	NP_775907.4:p.Arg839=
NM_173636.5:c.2515C=	NP_775907.4:p.Arg839=
ENST00000270301.11:c.2515C=	ENSP00000270301.6:p.Arg839=
ENST00000270301.12:c.2515C=	ENSP00000270301.6:p.Arg839=
ENST00000401500.6:c.2515C=	ENSP00000384792.1:p.Arg839=
ENST00000587391.5:c.*1205C=	ENSP00000465525.1:n.*1205C=
ENST00000587391.6:c.*1205C=	ENSP00000465525.1:n.*1205C=
ENST00000679357.1:c.305C=
ENST00000679422.1:c.305C=
ENST00000679682.1:c.2500C=	ENSP00000506226.1:p.Arg834=
ENST00000679714.1:c.2509C=	ENSP00000506627.1:p.Arg837=
ENST00000679757.1:c.2164C=	ENSP00000505158.1:p.Arg722=
ENST00000679858.1:c.*1312C=	ENSP00000505655.1:n.*1312C=
ENST00000680349.1:n.498C=
ENST00000680377.1:c.789C=
ENST00000680403.1:c.2515C=	ENSP00000505677.1:p.Arg839=
ENST00000680564.1:c.2515C=	ENSP00000505582.1:p.Arg839=
ENST00000680590.1:c.*914C=	ENSP00000505350.1:n.*914C=
ENST00000680806.1:c.*1344C=	ENSP00000506418.1:n.*1344C=
ENST00000680858.1:c.713C=
ENST00000681088.1:c.305C=
ENST00000681302.1:c.901C=
ENST00000681625.1:c.2500C=	ENSP00000505555.1:p.Arg834=
XM_005258809.2:c.2515C=	XP_005258866.1:p.Arg839=
XM_011526837.1:c.2500C=	XP_011525139.1:p.Arg834=
XM_011526838.1:c.2515C=	XP_011525140.1:p.Arg839=
XM_011526839.1:c.2164C=	XP_011525141.1:p.Arg722=
XM_011526840.1:c.1507C=	XP_011525142.1:p.Arg503=
XM_011526840.2:c.1507C=	XP_011525142.1:p.Arg503=
XM_011526841.1:c.1093C=	XP_011525143.1:p.Arg365=
XM_011526841.2:c.1093C=	XP_011525143.1:p.Arg365=
XM_011526842.1:c.946C=	XP_011525144.1:p.Arg316=
XM_011526843.1:c.262C=	XP_011525145.1:p.Arg88=
XM_011526844.1:c.262C=	XP_011525146.1:p.Arg88=
XM_011526844.2:c.262C=	XP_011525146.1:p.Arg88=
XM_017026665.1:c.2515C=	XP_016882154.1:p.Arg839=