Canonical Allele Identifier: CA2333970736

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101710C= , CM000681.2:g.36101710C=	GRCh38
NC_000019.9:g.36592612C= , CM000681.1:g.36592612C=	GRCh37
NC_000019.8:g.41284452C=	NCBI36
NG_028101.1:g.51830C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3018C=	ENSP00000270301.6:p.Ile1006=
ENST00000401500.7:c.3018C= MANE Select	ENSP00000384792.1:p.Ile1006=
ENST00000587391.6:c.*2054C=	ENSP00000465525.1:n.*2054C=
ENST00000679357.1:c.808C=
ENST00000679422.1:c.762-304C=
ENST00000679682.1:c.3003C=	ENSP00000506226.1:p.Ile1001=
ENST00000679714.1:c.3012C=	ENSP00000506627.1:p.Ile1004=
ENST00000679757.1:c.2667C=	ENSP00000505158.1:p.Ile889=
ENST00000679858.1:c.*2161C=	ENSP00000505655.1:n.*2161C=
ENST00000680211.1:c.-382C=	ENSP00000506102.1:n.-382C=
ENST00000680349.1:n.1001C=
ENST00000680403.1:c.3018C=	ENSP00000505677.1:p.Ile1006=
ENST00000680564.1:c.2971+393C=	ENSP00000505582.1:n.2971+393C=
ENST00000680590.1:c.*1413C=	ENSP00000505350.1:n.*1413C=
ENST00000680773.1:n.695C=
ENST00000680806.1:c.*1801-304C=	ENSP00000506418.1:n.*1801-304C=
ENST00000680997.1:n.365C=
ENST00000681088.1:c.680C=
ENST00000681625.1:c.*350C=	ENSP00000505555.1:n.*350C=
ENST00000270301.11:c.3018C=	ENSP00000270301.6:p.Ile1006=
ENST00000401500.6:c.3018C=	ENSP00000384792.1:p.Ile1006=
ENST00000587391.5:c.*2054C=	ENSP00000465525.1:n.*2054C=
NM_001083961.1:c.3018C=	NP_001077430.1:p.Ile1006=
NM_173636.4:c.3018C=	NP_775907.4:p.Ile1006=
XM_005258809.2:c.2972-304C=	XP_005258866.1:n.2972-304C=
XM_011526837.1:c.3003C=	XP_011525139.1:p.Ile1001=
XM_011526838.1:c.2971+393C=	XP_011525140.1:n.2971+393C=
XM_011526839.1:c.2667C=	XP_011525141.1:p.Ile889=
XM_011526840.1:c.2010C=	XP_011525142.1:p.Ile670=
XM_011526841.1:c.1596C=	XP_011525143.1:p.Ile532=
XM_011526842.1:c.1449C=	XP_011525144.1:p.Ile483=
XM_011526843.1:c.765C=	XP_011525145.1:p.Ile255=
XM_011526844.1:c.765C=	XP_011525146.1:p.Ile255=
XM_011526840.2:c.2010C=	XP_011525142.1:p.Ile670=
XM_011526841.2:c.1596C=	XP_011525143.1:p.Ile532=
XM_011526844.2:c.765C=	XP_011525146.1:p.Ile255=
XM_017026665.1:c.3018C=	XP_016882154.1:p.Ile1006=
NM_001083961.2:c.3018C= MANE Select	NP_001077430.1:p.Ile1006=
NM_173636.5:c.3018C=	NP_775907.4:p.Ile1006=