Canonical Allele Identifier: CA2333966467

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36092741C= , CM000681.2:g.36092741C=	GRCh38
NC_000019.9:g.36583643C= , CM000681.1:g.36583643C=	GRCh37
NC_000019.8:g.41275483C=	NCBI36
NG_028101.1:g.42861C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001083961.2:c.2263C= MANE Select	NP_001077430.1:p.His755=
ENST00000401500.7:c.2263C= MANE Select	ENSP00000384792.1:p.His755=
NM_001083961.1:c.2263C=	NP_001077430.1:p.His755=
NM_173636.4:c.2263C=	NP_775907.4:p.His755=
NM_173636.5:c.2263C=	NP_775907.4:p.His755=
ENST00000270301.11:c.2263C=	ENSP00000270301.6:p.His755=
ENST00000270301.12:c.2263C=	ENSP00000270301.6:p.His755=
ENST00000401500.6:c.2263C=	ENSP00000384792.1:p.His755=
ENST00000587391.5:c.*953C=	ENSP00000465525.1:n.*953C=
ENST00000587391.6:c.*953C=	ENSP00000465525.1:n.*953C=
ENST00000679357.1:c.53C=
ENST00000679422.1:c.53C=
ENST00000679682.1:c.2248C=	ENSP00000506226.1:p.His750=
ENST00000679714.1:c.2257C=	ENSP00000506627.1:p.His753=
ENST00000679757.1:c.1912C=	ENSP00000505158.1:p.His638=
ENST00000679858.1:c.*1060C=	ENSP00000505655.1:n.*1060C=
ENST00000680349.1:n.246C=
ENST00000680377.1:c.537C=
ENST00000680403.1:c.2263C=	ENSP00000505677.1:p.His755=
ENST00000680489.1:n.2586C=
ENST00000680564.1:c.2263C=	ENSP00000505582.1:p.His755=
ENST00000680590.1:c.*662C=	ENSP00000505350.1:n.*662C=
ENST00000680806.1:c.*1092C=	ENSP00000506418.1:n.*1092C=
ENST00000680858.1:c.461C=
ENST00000681088.1:c.53C=
ENST00000681302.1:c.649C=
ENST00000681625.1:c.2248C=	ENSP00000505555.1:p.His750=
XM_005258809.2:c.2263C=	XP_005258866.1:p.His755=
XM_011526837.1:c.2248C=	XP_011525139.1:p.His750=
XM_011526838.1:c.2263C=	XP_011525140.1:p.His755=
XM_011526839.1:c.1912C=	XP_011525141.1:p.His638=
XM_011526840.1:c.1255C=	XP_011525142.1:p.His419=
XM_011526840.2:c.1255C=	XP_011525142.1:p.His419=
XM_011526841.1:c.841C=	XP_011525143.1:p.His281=
XM_011526841.2:c.841C=	XP_011525143.1:p.His281=
XM_011526842.1:c.694C=	XP_011525144.1:p.His232=
XM_011526843.1:c.10C=	XP_011525145.1:p.His4=
XM_011526844.1:c.10C=	XP_011525146.1:p.His4=
XM_011526844.2:c.10C=	XP_011525146.1:p.His4=
XM_017026665.1:c.2263C=	XP_016882154.1:p.His755=
XR_001753671.1:n.2290C=
XR_001753672.1:n.2178C=