Canonical Allele Identifier: CA2333970920

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102063C= , CM000681.2:g.36102063C=	GRCh38
NC_000019.9:g.36592965C= , CM000681.1:g.36592965C=	GRCh37
NC_000019.8:g.41284805C=	NCBI36
NG_028101.1:g.52183C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3132C=	ENSP00000270301.6:p.Ser1044=
ENST00000401500.7:c.3132C= MANE Select	ENSP00000384792.1:p.Ser1044=
ENST00000587391.6:c.*2407C=	ENSP00000465525.1:n.*2407C=
ENST00000679357.1:c.922C=
ENST00000679422.1:c.811C=
ENST00000679682.1:c.3117C=	ENSP00000506226.1:p.Ser1039=
ENST00000679714.1:c.3126C=	ENSP00000506627.1:p.Ser1042=
ENST00000679757.1:c.2781C=	ENSP00000505158.1:p.Ser927=
ENST00000679858.1:c.*2514C=	ENSP00000505655.1:n.*2514C=
ENST00000680211.1:c.-268C=	ENSP00000506102.1:n.-268C=
ENST00000680349.1:n.1115C=
ENST00000680403.1:c.3132C=	ENSP00000505677.1:p.Ser1044=
ENST00000680564.1:c.2972-674C=	ENSP00000505582.1:n.2972-674C=
ENST00000680590.1:c.*1527C=	ENSP00000505350.1:n.*1527C=
ENST00000680739.1:c.50C=
ENST00000680773.1:n.1048C=
ENST00000680806.1:c.*1850C=	ENSP00000506418.1:n.*1850C=
ENST00000680997.1:n.479C=
ENST00000681088.1:c.794C=
ENST00000681608.1:n.80C=
ENST00000681625.1:c.*464C=	ENSP00000505555.1:n.*464C=
ENST00000270301.11:c.3132C=	ENSP00000270301.6:p.Ser1044=
ENST00000401500.6:c.3132C=	ENSP00000384792.1:p.Ser1044=
ENST00000587391.5:c.*2407C=	ENSP00000465525.1:n.*2407C=
NM_001083961.1:c.3132C=	NP_001077430.1:p.Ser1044=
NM_173636.4:c.3132C=	NP_775907.4:p.Ser1044=
XM_005258809.2:c.3021C=	XP_005258866.1:p.Ser1007=
XM_011526837.1:c.3117C=	XP_011525139.1:p.Ser1039=
XM_011526838.1:c.2972-674C=	XP_011525140.1:n.2972-674C=
XM_011526839.1:c.2781C=	XP_011525141.1:p.Ser927=
XM_011526840.1:c.2124C=	XP_011525142.1:p.Ser708=
XM_011526841.1:c.1710C=	XP_011525143.1:p.Ser570=
XM_011526842.1:c.1563C=	XP_011525144.1:p.Ser521=
XM_011526843.1:c.879C=	XP_011525145.1:p.Ser293=
XM_011526844.1:c.879C=	XP_011525146.1:p.Ser293=
XM_011526840.2:c.2124C=	XP_011525142.1:p.Ser708=
XM_011526841.2:c.1710C=	XP_011525143.1:p.Ser570=
XM_011526844.2:c.879C=	XP_011525146.1:p.Ser293=
XM_017026665.1:c.3132C=	XP_016882154.1:p.Ser1044=
NM_001083961.2:c.3132C= MANE Select	NP_001077430.1:p.Ser1044=
NM_173636.5:c.3132C=	NP_775907.4:p.Ser1044=