Canonical Allele Identifier: CA405448955

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592574G>A (hg19) ; chr19:g.36101672G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101672G>A , CM000681.2:g.36101672G>A	GRCh38
NC_000019.9:g.36592574G>A , CM000681.1:g.36592574G>A	GRCh37
NC_000019.8:g.41284414G>A	NCBI36
NG_028101.1:g.51792G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.2980G>A	ENSP00000270301.6:p.Glu994Lys
ENST00000401500.7:c.2980G>A MANE Select	ENSP00000384792.1:p.Glu994Lys
ENST00000587391.6:c.*2016G>A	ENSP00000465525.1:n.*2016G>A
ENST00000679357.1:c.770G>A
ENST00000679422.1:c.762-342G>A
ENST00000679682.1:c.2965G>A	ENSP00000506226.1:p.Glu989Lys
ENST00000679714.1:c.2974G>A	ENSP00000506627.1:p.Glu992Lys
ENST00000679757.1:c.2629G>A	ENSP00000505158.1:p.Glu877Lys
ENST00000679858.1:c.*2123G>A	ENSP00000505655.1:n.*2123G>A
ENST00000680211.1:c.-420G>A	ENSP00000506102.1:n.-420G>A
ENST00000680349.1:n.963G>A
ENST00000680403.1:c.2980G>A	ENSP00000505677.1:p.Glu994Lys
ENST00000680564.1:c.2971+355G>A	ENSP00000505582.1:n.2971+355G>A
ENST00000680590.1:c.*1375G>A	ENSP00000505350.1:n.*1375G>A
ENST00000680773.1:n.657G>A
ENST00000680806.1:c.*1801-342G>A	ENSP00000506418.1:n.*1801-342G>A
ENST00000680997.1:n.327G>A
ENST00000681088.1:c.642G>A
ENST00000681625.1:c.*312G>A	ENSP00000505555.1:n.*312G>A
ENST00000270301.11:c.2980G>A	ENSP00000270301.6:p.Glu994Lys
ENST00000401500.6:c.2980G>A	ENSP00000384792.1:p.Glu994Lys
ENST00000587391.5:c.*2016G>A	ENSP00000465525.1:n.*2016G>A
NM_001083961.1:c.2980G>A	NP_001077430.1:p.Glu994Lys
NM_173636.4:c.2980G>A	NP_775907.4:p.Glu994Lys
XM_005258809.2:c.2972-342G>A	XP_005258866.1:n.2972-342G>A
XM_011526837.1:c.2965G>A	XP_011525139.1:p.Glu989Lys
XM_011526838.1:c.2971+355G>A	XP_011525140.1:n.2971+355G>A
XM_011526839.1:c.2629G>A	XP_011525141.1:p.Glu877Lys
XM_011526840.1:c.1972G>A	XP_011525142.1:p.Glu658Lys
XM_011526841.1:c.1558G>A	XP_011525143.1:p.Glu520Lys
XM_011526842.1:c.1411G>A	XP_011525144.1:p.Glu471Lys
XM_011526843.1:c.727G>A	XP_011525145.1:p.Glu243Lys
XM_011526844.1:c.727G>A	XP_011525146.1:p.Glu243Lys
XM_011526840.2:c.1972G>A	XP_011525142.1:p.Glu658Lys
XM_011526841.2:c.1558G>A	XP_011525143.1:p.Glu520Lys
XM_011526844.2:c.727G>A	XP_011525146.1:p.Glu243Lys
XM_017026665.1:c.2980G>A	XP_016882154.1:p.Glu994Lys
NM_001083961.2:c.2980G>A MANE Select	NP_001077430.1:p.Glu994Lys
NM_173636.5:c.2980G>A	NP_775907.4:p.Glu994Lys