Canonical Allele Identifier: CA405460885

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104601-G-A
• MyVariant Identifiers: chr19:g.36595503G>A (hg19) ; chr19:g.36104601G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104601G>A , CM000681.2:g.36104601G>A	GRCh38
NC_000019.9:g.36595503G>A , CM000681.1:g.36595503G>A	GRCh37
NC_000019.8:g.41287343G>A	NCBI36
NG_028101.1:g.54721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4222G>A	ENSP00000270301.6:p.Glu1408Lys
ENST00000401500.7:c.4237G>A MANE Select	ENSP00000384792.1:p.Glu1413Lys
ENST00000587391.6:c.*4097G>A	ENSP00000465525.1:n.*4097G>A
ENST00000679357.1:c.2317G>A
ENST00000679598.1:c.982G>A
ENST00000679682.1:c.4222G>A	ENSP00000506226.1:p.Glu1408Lys
ENST00000679714.1:c.4231G>A	ENSP00000506627.1:p.Glu1411Lys
ENST00000679757.1:c.3886G>A	ENSP00000505158.1:p.Glu1296Lys
ENST00000679858.1:c.*3619G>A	ENSP00000505655.1:n.*3619G>A
ENST00000680211.1:c.838G>A	ENSP00000506102.1:p.Glu280Lys
ENST00000680280.1:n.1740G>A
ENST00000680349.1:n.2886G>A
ENST00000680403.1:c.4222G>A	ENSP00000505677.1:p.Glu1408Lys
ENST00000680564.1:c.3988G>A	ENSP00000505582.1:p.Glu1330Lys
ENST00000680590.1:c.*2617G>A	ENSP00000505350.1:n.*2617G>A
ENST00000680597.1:c.970G>A
ENST00000680739.1:c.1252G>A
ENST00000680773.1:n.2738G>A
ENST00000680806.1:c.*3540G>A	ENSP00000506418.1:n.*3540G>A
ENST00000680997.1:n.2169G>A
ENST00000681608.1:n.2082G>A
ENST00000681625.1:c.*1569G>A	ENSP00000505555.1:n.*1569G>A
ENST00000681648.1:n.2288G>A
ENST00000270301.11:c.4222G>A	ENSP00000270301.6:p.Glu1408Lys
ENST00000401500.6:c.4237G>A	ENSP00000384792.1:p.Glu1413Lys
ENST00000587391.5:c.*4097G>A	ENSP00000465525.1:n.*4097G>A
NM_001083961.1:c.4237G>A	NP_001077430.1:p.Glu1413Lys
NM_173636.4:c.4222G>A	NP_775907.4:p.Glu1408Lys
XM_005258809.2:c.4126G>A	XP_005258866.1:p.Glu1376Lys
XM_011526837.1:c.4222G>A	XP_011525139.1:p.Glu1408Lys
XM_011526838.1:c.3988G>A	XP_011525140.1:p.Glu1330Lys
XM_011526839.1:c.3886G>A	XP_011525141.1:p.Glu1296Lys
XM_011526840.1:c.3229G>A	XP_011525142.1:p.Glu1077Lys
XM_011526841.1:c.2815G>A	XP_011525143.1:p.Glu939Lys
XM_011526842.1:c.2668G>A	XP_011525144.1:p.Glu890Lys
XM_011526843.1:c.1984G>A	XP_011525145.1:p.Glu662Lys
XM_011526844.1:c.1984G>A	XP_011525146.1:p.Glu662Lys
XM_011526840.2:c.3229G>A	XP_011525142.1:p.Glu1077Lys
XM_011526841.2:c.2815G>A	XP_011525143.1:p.Glu939Lys
XM_011526844.2:c.1984G>A	XP_011525146.1:p.Glu662Lys
XM_017026665.1:c.4237G>A	XP_016882154.1:p.Glu1413Lys
NM_001083961.2:c.4237G>A MANE Select	NP_001077430.1:p.Glu1413Lys
NM_173636.5:c.4222G>A	NP_775907.4:p.Glu1408Lys