Canonical Allele Identifier: CA405460501

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595462A>T (hg19) ; chr19:g.36104560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104560A>T , CM000681.2:g.36104560A>T	GRCh38
NC_000019.9:g.36595462A>T , CM000681.1:g.36595462A>T	GRCh37
NC_000019.8:g.41287302A>T	NCBI36
NG_028101.1:g.54680A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4181A>T	ENSP00000270301.6:p.Glu1394Val
ENST00000401500.7:c.4196A>T MANE Select	ENSP00000384792.1:p.Glu1399Val
ENST00000587391.6:c.*4056A>T	ENSP00000465525.1:n.*4056A>T
ENST00000679357.1:c.2276A>T
ENST00000679598.1:c.941A>T
ENST00000679682.1:c.4181A>T	ENSP00000506226.1:p.Glu1394Val
ENST00000679714.1:c.4190A>T	ENSP00000506627.1:p.Glu1397Val
ENST00000679757.1:c.3845A>T	ENSP00000505158.1:p.Glu1282Val
ENST00000679858.1:c.*3578A>T	ENSP00000505655.1:n.*3578A>T
ENST00000680211.1:c.797A>T	ENSP00000506102.1:p.Glu266Val
ENST00000680280.1:n.1699A>T
ENST00000680349.1:n.2845A>T
ENST00000680403.1:c.4181A>T	ENSP00000505677.1:p.Glu1394Val
ENST00000680564.1:c.3947A>T	ENSP00000505582.1:p.Glu1316Val
ENST00000680590.1:c.*2576A>T	ENSP00000505350.1:n.*2576A>T
ENST00000680597.1:c.929A>T
ENST00000680739.1:c.1211A>T
ENST00000680773.1:n.2697A>T
ENST00000680806.1:c.*3499A>T	ENSP00000506418.1:n.*3499A>T
ENST00000680997.1:n.2128A>T
ENST00000681608.1:n.2041A>T
ENST00000681625.1:c.*1528A>T	ENSP00000505555.1:n.*1528A>T
ENST00000681648.1:n.2247A>T
ENST00000270301.11:c.4181A>T	ENSP00000270301.6:p.Glu1394Val
ENST00000401500.6:c.4196A>T	ENSP00000384792.1:p.Glu1399Val
ENST00000587391.5:c.*4056A>T	ENSP00000465525.1:n.*4056A>T
NM_001083961.1:c.4196A>T	NP_001077430.1:p.Glu1399Val
NM_173636.4:c.4181A>T	NP_775907.4:p.Glu1394Val
XM_005258809.2:c.4085A>T	XP_005258866.1:p.Glu1362Val
XM_011526837.1:c.4181A>T	XP_011525139.1:p.Glu1394Val
XM_011526838.1:c.3947A>T	XP_011525140.1:p.Glu1316Val
XM_011526839.1:c.3845A>T	XP_011525141.1:p.Glu1282Val
XM_011526840.1:c.3188A>T	XP_011525142.1:p.Glu1063Val
XM_011526841.1:c.2774A>T	XP_011525143.1:p.Glu925Val
XM_011526842.1:c.2627A>T	XP_011525144.1:p.Glu876Val
XM_011526843.1:c.1943A>T	XP_011525145.1:p.Glu648Val
XM_011526844.1:c.1943A>T	XP_011525146.1:p.Glu648Val
XM_011526840.2:c.3188A>T	XP_011525142.1:p.Glu1063Val
XM_011526841.2:c.2774A>T	XP_011525143.1:p.Glu925Val
XM_011526844.2:c.1943A>T	XP_011525146.1:p.Glu648Val
XM_017026665.1:c.4196A>T	XP_016882154.1:p.Glu1399Val
NM_001083961.2:c.4196A>T MANE Select	NP_001077430.1:p.Glu1399Val
NM_173636.5:c.4181A>T	NP_775907.4:p.Glu1394Val