Canonical Allele Identifier: CA2333972177

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104523C= , CM000681.2:g.36104523C=	GRCh38
NC_000019.9:g.36595425C= , CM000681.1:g.36595425C=	GRCh37
NC_000019.8:g.41287265C=	NCBI36
NG_028101.1:g.54643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4144C=	ENSP00000270301.6:p.Leu1382=
ENST00000401500.7:c.4159C= MANE Select	ENSP00000384792.1:p.Leu1387=
ENST00000587391.6:c.*4019C=	ENSP00000465525.1:n.*4019C=
ENST00000679357.1:c.2239C=
ENST00000679598.1:c.919-15C=
ENST00000679682.1:c.4144C=	ENSP00000506226.1:p.Leu1382=
ENST00000679714.1:c.4153C=	ENSP00000506627.1:p.Leu1385=
ENST00000679757.1:c.3808C=	ENSP00000505158.1:p.Leu1270=
ENST00000679858.1:c.*3541C=	ENSP00000505655.1:n.*3541C=
ENST00000680211.1:c.760C=	ENSP00000506102.1:p.Leu254=
ENST00000680280.1:n.1662C=
ENST00000680349.1:n.2808C=
ENST00000680403.1:c.4144C=	ENSP00000505677.1:p.Leu1382=
ENST00000680564.1:c.3910C=	ENSP00000505582.1:p.Leu1304=
ENST00000680590.1:c.*2539C=	ENSP00000505350.1:n.*2539C=
ENST00000680597.1:c.892C=
ENST00000680739.1:c.1174C=
ENST00000680773.1:n.2660C=
ENST00000680806.1:c.*3462C=	ENSP00000506418.1:n.*3462C=
ENST00000680997.1:n.2091C=
ENST00000681608.1:n.2004C=
ENST00000681625.1:c.*1491C=	ENSP00000505555.1:n.*1491C=
ENST00000681648.1:n.2210C=
ENST00000270301.11:c.4144C=	ENSP00000270301.6:p.Leu1382=
ENST00000401500.6:c.4159C=	ENSP00000384792.1:p.Leu1387=
ENST00000587391.5:c.*4019C=	ENSP00000465525.1:n.*4019C=
NM_001083961.1:c.4159C=	NP_001077430.1:p.Leu1387=
NM_173636.4:c.4144C=	NP_775907.4:p.Leu1382=
XM_005258809.2:c.4048C=	XP_005258866.1:p.Leu1350=
XM_011526837.1:c.4144C=	XP_011525139.1:p.Leu1382=
XM_011526838.1:c.3910C=	XP_011525140.1:p.Leu1304=
XM_011526839.1:c.3808C=	XP_011525141.1:p.Leu1270=
XM_011526840.1:c.3151C=	XP_011525142.1:p.Leu1051=
XM_011526841.1:c.2737C=	XP_011525143.1:p.Leu913=
XM_011526842.1:c.2590C=	XP_011525144.1:p.Leu864=
XM_011526843.1:c.1906C=	XP_011525145.1:p.Leu636=
XM_011526844.1:c.1906C=	XP_011525146.1:p.Leu636=
XM_011526840.2:c.3151C=	XP_011525142.1:p.Leu1051=
XM_011526841.2:c.2737C=	XP_011525143.1:p.Leu913=
XM_011526844.2:c.1906C=	XP_011525146.1:p.Leu636=
XM_017026665.1:c.4159C=	XP_016882154.1:p.Leu1387=
NM_001083961.2:c.4159C= MANE Select	NP_001077430.1:p.Leu1387=
NM_173636.5:c.4144C=	NP_775907.4:p.Leu1382=