Canonical Allele Identifier: CA2333970713

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101669G= , CM000681.2:g.36101669G=	GRCh38
NC_000019.9:g.36592571G= , CM000681.1:g.36592571G=	GRCh37
NC_000019.8:g.41284411G=	NCBI36
NG_028101.1:g.51789G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.2977G=	ENSP00000270301.6:p.Gly993=
ENST00000401500.7:c.2977G= MANE Select	ENSP00000384792.1:p.Gly993=
ENST00000587391.6:c.*2013G=	ENSP00000465525.1:n.*2013G=
ENST00000679357.1:c.767G=
ENST00000679422.1:c.762-345G=
ENST00000679682.1:c.2962G=	ENSP00000506226.1:p.Gly988=
ENST00000679714.1:c.2971G=	ENSP00000506627.1:p.Gly991=
ENST00000679757.1:c.2626G=	ENSP00000505158.1:p.Gly876=
ENST00000679858.1:c.*2120G=	ENSP00000505655.1:n.*2120G=
ENST00000680211.1:c.-423G=	ENSP00000506102.1:n.-423G=
ENST00000680349.1:n.960G=
ENST00000680403.1:c.2977G=	ENSP00000505677.1:p.Gly993=
ENST00000680564.1:c.2971+352G=	ENSP00000505582.1:n.2971+352G=
ENST00000680590.1:c.*1372G=	ENSP00000505350.1:n.*1372G=
ENST00000680773.1:n.654G=
ENST00000680806.1:c.*1801-345G=	ENSP00000506418.1:n.*1801-345G=
ENST00000680997.1:n.324G=
ENST00000681088.1:c.639G=
ENST00000681625.1:c.*309G=	ENSP00000505555.1:n.*309G=
ENST00000270301.11:c.2977G=	ENSP00000270301.6:p.Gly993=
ENST00000401500.6:c.2977G=	ENSP00000384792.1:p.Gly993=
ENST00000587391.5:c.*2013G=	ENSP00000465525.1:n.*2013G=
NM_001083961.1:c.2977G=	NP_001077430.1:p.Gly993=
NM_173636.4:c.2977G=	NP_775907.4:p.Gly993=
XM_005258809.2:c.2972-345G=	XP_005258866.1:n.2972-345G=
XM_011526837.1:c.2962G=	XP_011525139.1:p.Gly988=
XM_011526838.1:c.2971+352G=	XP_011525140.1:n.2971+352G=
XM_011526839.1:c.2626G=	XP_011525141.1:p.Gly876=
XM_011526840.1:c.1969G=	XP_011525142.1:p.Gly657=
XM_011526841.1:c.1555G=	XP_011525143.1:p.Gly519=
XM_011526842.1:c.1408G=	XP_011525144.1:p.Gly470=
XM_011526843.1:c.724G=	XP_011525145.1:p.Gly242=
XM_011526844.1:c.724G=	XP_011525146.1:p.Gly242=
XM_011526840.2:c.1969G=	XP_011525142.1:p.Gly657=
XM_011526841.2:c.1555G=	XP_011525143.1:p.Gly519=
XM_011526844.2:c.724G=	XP_011525146.1:p.Gly242=
XM_017026665.1:c.2977G=	XP_016882154.1:p.Gly993=
NM_001083961.2:c.2977G= MANE Select	NP_001077430.1:p.Gly993=
NM_173636.5:c.2977G=	NP_775907.4:p.Gly993=