Canonical Allele Identifier: CA405450698

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102119-A-G
• MyVariant Identifiers: chr19:g.36593021A>G (hg19) ; chr19:g.36102119A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102119A>G , CM000681.2:g.36102119A>G	GRCh38
NC_000019.9:g.36593021A>G , CM000681.1:g.36593021A>G	GRCh37
NC_000019.8:g.41284861A>G	NCBI36
NG_028101.1:g.52239A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3188A>G	ENSP00000270301.6:p.His1063Arg
ENST00000401500.7:c.3188A>G MANE Select	ENSP00000384792.1:p.His1063Arg
ENST00000587391.6:c.*2463A>G	ENSP00000465525.1:n.*2463A>G
ENST00000679357.1:c.978A>G
ENST00000679422.1:c.867A>G
ENST00000679682.1:c.3173A>G	ENSP00000506226.1:p.His1058Arg
ENST00000679714.1:c.3182A>G	ENSP00000506627.1:p.His1061Arg
ENST00000679757.1:c.2837A>G	ENSP00000505158.1:p.His946Arg
ENST00000679858.1:c.*2570A>G	ENSP00000505655.1:n.*2570A>G
ENST00000680211.1:c.-212A>G	ENSP00000506102.1:n.-212A>G
ENST00000680349.1:n.1171A>G
ENST00000680403.1:c.3188A>G	ENSP00000505677.1:p.His1063Arg
ENST00000680564.1:c.2972-618A>G	ENSP00000505582.1:n.2972-618A>G
ENST00000680590.1:c.*1583A>G	ENSP00000505350.1:n.*1583A>G
ENST00000680739.1:c.106A>G
ENST00000680773.1:n.1104A>G
ENST00000680806.1:c.*1906A>G	ENSP00000506418.1:n.*1906A>G
ENST00000680997.1:n.535A>G
ENST00000681088.1:c.850A>G
ENST00000681608.1:n.136A>G
ENST00000681625.1:c.*520A>G	ENSP00000505555.1:n.*520A>G
ENST00000270301.11:c.3188A>G	ENSP00000270301.6:p.His1063Arg
ENST00000401500.6:c.3188A>G	ENSP00000384792.1:p.His1063Arg
ENST00000587391.5:c.*2463A>G	ENSP00000465525.1:n.*2463A>G
NM_001083961.1:c.3188A>G	NP_001077430.1:p.His1063Arg
NM_173636.4:c.3188A>G	NP_775907.4:p.His1063Arg
XM_005258809.2:c.3077A>G	XP_005258866.1:p.His1026Arg
XM_011526837.1:c.3173A>G	XP_011525139.1:p.His1058Arg
XM_011526838.1:c.2972-618A>G	XP_011525140.1:n.2972-618A>G
XM_011526839.1:c.2837A>G	XP_011525141.1:p.His946Arg
XM_011526840.1:c.2180A>G	XP_011525142.1:p.His727Arg
XM_011526841.1:c.1766A>G	XP_011525143.1:p.His589Arg
XM_011526842.1:c.1619A>G	XP_011525144.1:p.His540Arg
XM_011526843.1:c.935A>G	XP_011525145.1:p.His312Arg
XM_011526844.1:c.935A>G	XP_011525146.1:p.His312Arg
XM_011526840.2:c.2180A>G	XP_011525142.1:p.His727Arg
XM_011526841.2:c.1766A>G	XP_011525143.1:p.His589Arg
XM_011526844.2:c.935A>G	XP_011525146.1:p.His312Arg
XM_017026665.1:c.3188A>G	XP_016882154.1:p.His1063Arg
NM_001083961.2:c.3188A>G MANE Select	NP_001077430.1:p.His1063Arg
NM_173636.5:c.3188A>G	NP_775907.4:p.His1063Arg