Canonical Allele Identifier: CA2333970903

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102023G= , CM000681.2:g.36102023G=	GRCh38
NC_000019.9:g.36592925G= , CM000681.1:g.36592925G=	GRCh37
NC_000019.8:g.41284765G=	NCBI36
NG_028101.1:g.52143G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3092G=	ENSP00000270301.6:p.Gly1031=
ENST00000401500.7:c.3092G= MANE Select	ENSP00000384792.1:p.Gly1031=
ENST00000587391.6:c.*2367G=	ENSP00000465525.1:n.*2367G=
ENST00000679357.1:c.882G=
ENST00000679422.1:c.771G=
ENST00000679682.1:c.3077G=	ENSP00000506226.1:p.Gly1026=
ENST00000679714.1:c.3086G=	ENSP00000506627.1:p.Gly1029=
ENST00000679757.1:c.2741G=	ENSP00000505158.1:p.Gly914=
ENST00000679858.1:c.*2474G=	ENSP00000505655.1:n.*2474G=
ENST00000680211.1:c.-308G=	ENSP00000506102.1:n.-308G=
ENST00000680349.1:n.1075G=
ENST00000680403.1:c.3092G=	ENSP00000505677.1:p.Gly1031=
ENST00000680564.1:c.2971+706G=	ENSP00000505582.1:n.2971+706G=
ENST00000680590.1:c.*1487G=	ENSP00000505350.1:n.*1487G=
ENST00000680739.1:c.10G=
ENST00000680773.1:n.1008G=
ENST00000680806.1:c.*1810G=	ENSP00000506418.1:n.*1810G=
ENST00000680997.1:n.439G=
ENST00000681088.1:c.754G=
ENST00000681608.1:n.40G=
ENST00000681625.1:c.*424G=	ENSP00000505555.1:n.*424G=
ENST00000270301.11:c.3092G=	ENSP00000270301.6:p.Gly1031=
ENST00000401500.6:c.3092G=	ENSP00000384792.1:p.Gly1031=
ENST00000587391.5:c.*2367G=	ENSP00000465525.1:n.*2367G=
NM_001083961.1:c.3092G=	NP_001077430.1:p.Gly1031=
NM_173636.4:c.3092G=	NP_775907.4:p.Gly1031=
XM_005258809.2:c.2981G=	XP_005258866.1:p.Gly994=
XM_011526837.1:c.3077G=	XP_011525139.1:p.Gly1026=
XM_011526838.1:c.2971+706G=	XP_011525140.1:n.2971+706G=
XM_011526839.1:c.2741G=	XP_011525141.1:p.Gly914=
XM_011526840.1:c.2084G=	XP_011525142.1:p.Gly695=
XM_011526841.1:c.1670G=	XP_011525143.1:p.Gly557=
XM_011526842.1:c.1523G=	XP_011525144.1:p.Gly508=
XM_011526843.1:c.839G=	XP_011525145.1:p.Gly280=
XM_011526844.1:c.839G=	XP_011525146.1:p.Gly280=
XM_011526840.2:c.2084G=	XP_011525142.1:p.Gly695=
XM_011526841.2:c.1670G=	XP_011525143.1:p.Gly557=
XM_011526844.2:c.839G=	XP_011525146.1:p.Gly280=
XM_017026665.1:c.3092G=	XP_016882154.1:p.Gly1031=
NM_001083961.2:c.3092G= MANE Select	NP_001077430.1:p.Gly1031=
NM_173636.5:c.3092G=	NP_775907.4:p.Gly1031=