Canonical Allele Identifier: CA2333970772

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101774G= , CM000681.2:g.36101774G=	GRCh38
NC_000019.9:g.36592676G= , CM000681.1:g.36592676G=	GRCh37
NC_000019.8:g.41284516G=	NCBI36
NG_028101.1:g.51894G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3082G=	ENSP00000270301.6:p.Gly1028=
ENST00000401500.7:c.3082G= MANE Select	ENSP00000384792.1:p.Gly1028=
ENST00000587391.6:c.*2118G=	ENSP00000465525.1:n.*2118G=
ENST00000679357.1:c.872G=
ENST00000679422.1:c.762-240G=
ENST00000679682.1:c.3067G=	ENSP00000506226.1:p.Gly1023=
ENST00000679714.1:c.3076G=	ENSP00000506627.1:p.Gly1026=
ENST00000679757.1:c.2731G=	ENSP00000505158.1:p.Gly911=
ENST00000679858.1:c.*2225G=	ENSP00000505655.1:n.*2225G=
ENST00000680211.1:c.-318G=	ENSP00000506102.1:n.-318G=
ENST00000680349.1:n.1065G=
ENST00000680403.1:c.3082G=	ENSP00000505677.1:p.Gly1028=
ENST00000680564.1:c.2971+457G=	ENSP00000505582.1:n.2971+457G=
ENST00000680590.1:c.*1477G=	ENSP00000505350.1:n.*1477G=
ENST00000680773.1:n.759G=
ENST00000680806.1:c.*1801-240G=	ENSP00000506418.1:n.*1801-240G=
ENST00000680997.1:n.429G=
ENST00000681088.1:c.744G=
ENST00000681608.1:n.30G=
ENST00000681625.1:c.*414G=	ENSP00000505555.1:n.*414G=
ENST00000270301.11:c.3082G=	ENSP00000270301.6:p.Gly1028=
ENST00000401500.6:c.3082G=	ENSP00000384792.1:p.Gly1028=
ENST00000587391.5:c.*2118G=	ENSP00000465525.1:n.*2118G=
NM_001083961.1:c.3082G=	NP_001077430.1:p.Gly1028=
NM_173636.4:c.3082G=	NP_775907.4:p.Gly1028=
XM_005258809.2:c.2972-240G=	XP_005258866.1:n.2972-240G=
XM_011526837.1:c.3067G=	XP_011525139.1:p.Gly1023=
XM_011526838.1:c.2971+457G=	XP_011525140.1:n.2971+457G=
XM_011526839.1:c.2731G=	XP_011525141.1:p.Gly911=
XM_011526840.1:c.2074G=	XP_011525142.1:p.Gly692=
XM_011526841.1:c.1660G=	XP_011525143.1:p.Gly554=
XM_011526842.1:c.1513G=	XP_011525144.1:p.Gly505=
XM_011526843.1:c.829G=	XP_011525145.1:p.Gly277=
XM_011526844.1:c.829G=	XP_011525146.1:p.Gly277=
XM_011526840.2:c.2074G=	XP_011525142.1:p.Gly692=
XM_011526841.2:c.1660G=	XP_011525143.1:p.Gly554=
XM_011526844.2:c.829G=	XP_011525146.1:p.Gly277=
XM_017026665.1:c.3082G=	XP_016882154.1:p.Gly1028=
NM_001083961.2:c.3082G= MANE Select	NP_001077430.1:p.Gly1028=
NM_173636.5:c.3082G=	NP_775907.4:p.Gly1028=