Canonical Allele Identifier: CA405460995

Gene: WDR62

Linked Data

• dbSNP Id: rs1317480309
• gnomAD v2: 19-36595515-G-A
• gnomAD v4: 19-36104613-G-A
• MyVariant Identifiers: chr19:g.36595515G>A (hg19) ; chr19:g.36104613G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104613G>A , CM000681.2:g.36104613G>A	GRCh38
NC_000019.9:g.36595515G>A , CM000681.1:g.36595515G>A	GRCh37
NC_000019.8:g.41287355G>A	NCBI36
NG_028101.1:g.54733G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4234G>A	ENSP00000270301.6:p.Val1412Met
ENST00000401500.7:c.4249G>A MANE Select	ENSP00000384792.1:p.Val1417Met
ENST00000587391.6:c.*4109G>A	ENSP00000465525.1:n.*4109G>A
ENST00000679357.1:c.2329G>A
ENST00000679598.1:c.994G>A
ENST00000679682.1:c.4234G>A	ENSP00000506226.1:p.Val1412Met
ENST00000679714.1:c.4243G>A	ENSP00000506627.1:p.Val1415Met
ENST00000679757.1:c.3898G>A	ENSP00000505158.1:p.Val1300Met
ENST00000679858.1:c.*3631G>A	ENSP00000505655.1:n.*3631G>A
ENST00000680211.1:c.850G>A	ENSP00000506102.1:p.Val284Met
ENST00000680280.1:n.1752G>A
ENST00000680349.1:n.2898G>A
ENST00000680403.1:c.4234G>A	ENSP00000505677.1:p.Val1412Met
ENST00000680564.1:c.4000G>A	ENSP00000505582.1:p.Val1334Met
ENST00000680590.1:c.*2629G>A	ENSP00000505350.1:n.*2629G>A
ENST00000680597.1:c.982G>A
ENST00000680739.1:c.1264G>A
ENST00000680773.1:n.2750G>A
ENST00000680806.1:c.*3552G>A	ENSP00000506418.1:n.*3552G>A
ENST00000680997.1:n.2181G>A
ENST00000681608.1:n.2094G>A
ENST00000681625.1:c.*1581G>A	ENSP00000505555.1:n.*1581G>A
ENST00000681648.1:n.2300G>A
ENST00000270301.11:c.4234G>A	ENSP00000270301.6:p.Val1412Met
ENST00000401500.6:c.4249G>A	ENSP00000384792.1:p.Val1417Met
ENST00000587391.5:c.*4109G>A	ENSP00000465525.1:n.*4109G>A
NM_001083961.1:c.4249G>A	NP_001077430.1:p.Val1417Met
NM_173636.4:c.4234G>A	NP_775907.4:p.Val1412Met
XM_005258809.2:c.4138G>A	XP_005258866.1:p.Val1380Met
XM_011526837.1:c.4234G>A	XP_011525139.1:p.Val1412Met
XM_011526838.1:c.4000G>A	XP_011525140.1:p.Val1334Met
XM_011526839.1:c.3898G>A	XP_011525141.1:p.Val1300Met
XM_011526840.1:c.3241G>A	XP_011525142.1:p.Val1081Met
XM_011526841.1:c.2827G>A	XP_011525143.1:p.Val943Met
XM_011526842.1:c.2680G>A	XP_011525144.1:p.Val894Met
XM_011526843.1:c.1996G>A	XP_011525145.1:p.Val666Met
XM_011526844.1:c.1996G>A	XP_011525146.1:p.Val666Met
XM_011526840.2:c.3241G>A	XP_011525142.1:p.Val1081Met
XM_011526841.2:c.2827G>A	XP_011525143.1:p.Val943Met
XM_011526844.2:c.1996G>A	XP_011525146.1:p.Val666Met
XM_017026665.1:c.4249G>A	XP_016882154.1:p.Val1417Met
NM_001083961.2:c.4249G>A MANE Select	NP_001077430.1:p.Val1417Met
NM_173636.5:c.4234G>A	NP_775907.4:p.Val1412Met