Canonical Allele Identifier: CA2333970957

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102135T= , CM000681.2:g.36102135T=	GRCh38
NC_000019.9:g.36593037T= , CM000681.1:g.36593037T=	GRCh37
NC_000019.8:g.41284877T=	NCBI36
NG_028101.1:g.52255T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3204T=	ENSP00000270301.6:p.Thr1068=
ENST00000401500.7:c.3204T= MANE Select	ENSP00000384792.1:p.Thr1068=
ENST00000587391.6:c.*2479T=	ENSP00000465525.1:n.*2479T=
ENST00000679357.1:c.994T=
ENST00000679422.1:c.883T=
ENST00000679682.1:c.3189T=	ENSP00000506226.1:p.Thr1063=
ENST00000679714.1:c.3198T=	ENSP00000506627.1:p.Thr1066=
ENST00000679757.1:c.2853T=	ENSP00000505158.1:p.Thr951=
ENST00000679858.1:c.*2586T=	ENSP00000505655.1:n.*2586T=
ENST00000680211.1:c.-196T=	ENSP00000506102.1:n.-196T=
ENST00000680349.1:n.1187T=
ENST00000680403.1:c.3204T=	ENSP00000505677.1:p.Thr1068=
ENST00000680564.1:c.2972-602T=	ENSP00000505582.1:n.2972-602T=
ENST00000680590.1:c.*1599T=	ENSP00000505350.1:n.*1599T=
ENST00000680739.1:c.122T=
ENST00000680773.1:n.1120T=
ENST00000680806.1:c.*1922T=	ENSP00000506418.1:n.*1922T=
ENST00000680997.1:n.551T=
ENST00000681088.1:c.866T=
ENST00000681608.1:n.152T=
ENST00000681625.1:c.*536T=	ENSP00000505555.1:n.*536T=
ENST00000270301.11:c.3204T=	ENSP00000270301.6:p.Thr1068=
ENST00000401500.6:c.3204T=	ENSP00000384792.1:p.Thr1068=
ENST00000587391.5:c.*2479T=	ENSP00000465525.1:n.*2479T=
NM_001083961.1:c.3204T=	NP_001077430.1:p.Thr1068=
NM_173636.4:c.3204T=	NP_775907.4:p.Thr1068=
XM_005258809.2:c.3093T=	XP_005258866.1:p.Thr1031=
XM_011526837.1:c.3189T=	XP_011525139.1:p.Thr1063=
XM_011526838.1:c.2972-602T=	XP_011525140.1:n.2972-602T=
XM_011526839.1:c.2853T=	XP_011525141.1:p.Thr951=
XM_011526840.1:c.2196T=	XP_011525142.1:p.Thr732=
XM_011526841.1:c.1782T=	XP_011525143.1:p.Thr594=
XM_011526842.1:c.1635T=	XP_011525144.1:p.Thr545=
XM_011526843.1:c.951T=	XP_011525145.1:p.Thr317=
XM_011526844.1:c.951T=	XP_011525146.1:p.Thr317=
XM_011526840.2:c.2196T=	XP_011525142.1:p.Thr732=
XM_011526841.2:c.1782T=	XP_011525143.1:p.Thr594=
XM_011526844.2:c.951T=	XP_011525146.1:p.Thr317=
XM_017026665.1:c.3204T=	XP_016882154.1:p.Thr1068=
NM_001083961.2:c.3204T= MANE Select	NP_001077430.1:p.Thr1068=
NM_173636.5:c.3204T=	NP_775907.4:p.Thr1068=