Canonical Allele Identifier: CA507318585

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595481A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104579A>G , CM000681.2:g.36104579A>G	GRCh38
NC_000019.9:g.36595481A>G , CM000681.1:g.36595481A>G	GRCh37
NC_000019.8:g.41287321A>G	NCBI36
NG_028101.1:g.54699A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4200A>G	ENSP00000270301.6:p.Glu1400=
ENST00000401500.7:c.4215A>G MANE Select	ENSP00000384792.1:p.Glu1405=
ENST00000587391.6:c.*4075A>G	ENSP00000465525.1:n.*4075A>G
ENST00000679357.1:c.2295A>G
ENST00000679598.1:c.960A>G
ENST00000679682.1:c.4200A>G	ENSP00000506226.1:p.Glu1400=
ENST00000679714.1:c.4209A>G	ENSP00000506627.1:p.Glu1403=
ENST00000679757.1:c.3864A>G	ENSP00000505158.1:p.Glu1288=
ENST00000679858.1:c.*3597A>G	ENSP00000505655.1:n.*3597A>G
ENST00000680211.1:c.816A>G	ENSP00000506102.1:p.Glu272=
ENST00000680280.1:n.1718A>G
ENST00000680349.1:n.2864A>G
ENST00000680403.1:c.4200A>G	ENSP00000505677.1:p.Glu1400=
ENST00000680564.1:c.3966A>G	ENSP00000505582.1:p.Glu1322=
ENST00000680590.1:c.*2595A>G	ENSP00000505350.1:n.*2595A>G
ENST00000680597.1:c.948A>G
ENST00000680739.1:c.1230A>G
ENST00000680773.1:n.2716A>G
ENST00000680806.1:c.*3518A>G	ENSP00000506418.1:n.*3518A>G
ENST00000680997.1:n.2147A>G
ENST00000681608.1:n.2060A>G
ENST00000681625.1:c.*1547A>G	ENSP00000505555.1:n.*1547A>G
ENST00000681648.1:n.2266A>G
ENST00000270301.11:c.4200A>G	ENSP00000270301.6:p.Glu1400=
ENST00000401500.6:c.4215A>G	ENSP00000384792.1:p.Glu1405=
ENST00000587391.5:c.*4075A>G	ENSP00000465525.1:n.*4075A>G
NM_001083961.1:c.4215A>G	NP_001077430.1:p.Glu1405=
NM_173636.4:c.4200A>G	NP_775907.4:p.Glu1400=
XM_005258809.2:c.4104A>G	XP_005258866.1:p.Glu1368=
XM_011526837.1:c.4200A>G	XP_011525139.1:p.Glu1400=
XM_011526838.1:c.3966A>G	XP_011525140.1:p.Glu1322=
XM_011526839.1:c.3864A>G	XP_011525141.1:p.Glu1288=
XM_011526840.1:c.3207A>G	XP_011525142.1:p.Glu1069=
XM_011526841.1:c.2793A>G	XP_011525143.1:p.Glu931=
XM_011526842.1:c.2646A>G	XP_011525144.1:p.Glu882=
XM_011526843.1:c.1962A>G	XP_011525145.1:p.Glu654=
XM_011526844.1:c.1962A>G	XP_011525146.1:p.Glu654=
XM_011526840.2:c.3207A>G	XP_011525142.1:p.Glu1069=
XM_011526841.2:c.2793A>G	XP_011525143.1:p.Glu931=
XM_011526844.2:c.1962A>G	XP_011525146.1:p.Glu654=
XM_017026665.1:c.4215A>G	XP_016882154.1:p.Glu1405=
NM_001083961.2:c.4215A>G MANE Select	NP_001077430.1:p.Glu1405=
NM_173636.5:c.4200A>G	NP_775907.4:p.Glu1400=