Canonical Allele Identifier: CA2333971389

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102972G= , CM000681.2:g.36102972G=	GRCh38
NC_000019.9:g.36593874G= , CM000681.1:g.36593874G=	GRCh37
NC_000019.8:g.41285714G=	NCBI36
NG_028101.1:g.53092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3345G=	ENSP00000270301.6:p.Arg1115=
ENST00000401500.7:c.3360G= MANE Select	ENSP00000384792.1:p.Arg1120=
ENST00000587391.6:c.*3220G=	ENSP00000465525.1:n.*3220G=
ENST00000679357.1:c.1440G=
ENST00000679598.1:c.125G=
ENST00000679682.1:c.3345G=	ENSP00000506226.1:p.Arg1115=
ENST00000679714.1:c.3354G=	ENSP00000506627.1:p.Arg1118=
ENST00000679757.1:c.3009G=	ENSP00000505158.1:p.Arg1003=
ENST00000679858.1:c.*2742G=	ENSP00000505655.1:n.*2742G=
ENST00000680211.1:c.-40G=	ENSP00000506102.1:n.-40G=
ENST00000680280.1:n.647G=
ENST00000680349.1:n.1928G=
ENST00000680403.1:c.3345G=	ENSP00000505677.1:p.Arg1115=
ENST00000680564.1:c.3111G=	ENSP00000505582.1:p.Arg1037=
ENST00000680590.1:c.*1740G=	ENSP00000505350.1:n.*1740G=
ENST00000680597.1:c.125G=
ENST00000680739.1:c.375G=
ENST00000680773.1:n.1861G=
ENST00000680806.1:c.*2663G=	ENSP00000506418.1:n.*2663G=
ENST00000680997.1:n.1292G=
ENST00000681608.1:n.989G=
ENST00000681625.1:c.*692G=	ENSP00000505555.1:n.*692G=
ENST00000681648.1:n.659G=
ENST00000270301.11:c.3345G=	ENSP00000270301.6:p.Arg1115=
ENST00000401500.6:c.3360G=	ENSP00000384792.1:p.Arg1120=
ENST00000587391.5:c.*3220G=	ENSP00000465525.1:n.*3220G=
NM_001083961.1:c.3360G=	NP_001077430.1:p.Arg1120=
NM_173636.4:c.3345G=	NP_775907.4:p.Arg1115=
XM_005258809.2:c.3249G=	XP_005258866.1:p.Arg1083=
XM_011526837.1:c.3345G=	XP_011525139.1:p.Arg1115=
XM_011526838.1:c.3111G=	XP_011525140.1:p.Arg1037=
XM_011526839.1:c.3009G=	XP_011525141.1:p.Arg1003=
XM_011526840.1:c.2352G=	XP_011525142.1:p.Arg784=
XM_011526841.1:c.1938G=	XP_011525143.1:p.Arg646=
XM_011526842.1:c.1791G=	XP_011525144.1:p.Arg597=
XM_011526843.1:c.1107G=	XP_011525145.1:p.Arg369=
XM_011526844.1:c.1107G=	XP_011525146.1:p.Arg369=
XM_011526840.2:c.2352G=	XP_011525142.1:p.Arg784=
XM_011526841.2:c.1938G=	XP_011525143.1:p.Arg646=
XM_011526844.2:c.1107G=	XP_011525146.1:p.Arg369=
XM_017026665.1:c.3360G=	XP_016882154.1:p.Arg1120=
NM_001083961.2:c.3360G= MANE Select	NP_001077430.1:p.Arg1120=
NM_173636.5:c.3345G=	NP_775907.4:p.Arg1115=