Canonical Allele Identifier: CA507318416

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104519-T-G
• MyVariant Identifiers: chr19:g.36595421T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104519T>G , CM000681.2:g.36104519T>G	GRCh38
NC_000019.9:g.36595421T>G , CM000681.1:g.36595421T>G	GRCh37
NC_000019.8:g.41287261T>G	NCBI36
NG_028101.1:g.54639T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4140T>G	ENSP00000270301.6:p.Gly1380=
ENST00000401500.7:c.4155T>G MANE Select	ENSP00000384792.1:p.Gly1385=
ENST00000587391.6:c.*4015T>G	ENSP00000465525.1:n.*4015T>G
ENST00000679357.1:c.2235T>G
ENST00000679598.1:c.919-19T>G
ENST00000679682.1:c.4140T>G	ENSP00000506226.1:p.Gly1380=
ENST00000679714.1:c.4149T>G	ENSP00000506627.1:p.Gly1383=
ENST00000679757.1:c.3804T>G	ENSP00000505158.1:p.Gly1268=
ENST00000679858.1:c.*3537T>G	ENSP00000505655.1:n.*3537T>G
ENST00000680211.1:c.756T>G	ENSP00000506102.1:p.Gly252=
ENST00000680280.1:n.1658T>G
ENST00000680349.1:n.2804T>G
ENST00000680403.1:c.4140T>G	ENSP00000505677.1:p.Gly1380=
ENST00000680564.1:c.3906T>G	ENSP00000505582.1:p.Gly1302=
ENST00000680590.1:c.*2535T>G	ENSP00000505350.1:n.*2535T>G
ENST00000680597.1:c.888T>G
ENST00000680739.1:c.1170T>G
ENST00000680773.1:n.2656T>G
ENST00000680806.1:c.*3458T>G	ENSP00000506418.1:n.*3458T>G
ENST00000680997.1:n.2087T>G
ENST00000681608.1:n.2000T>G
ENST00000681625.1:c.*1487T>G	ENSP00000505555.1:n.*1487T>G
ENST00000681648.1:n.2206T>G
ENST00000270301.11:c.4140T>G	ENSP00000270301.6:p.Gly1380=
ENST00000401500.6:c.4155T>G	ENSP00000384792.1:p.Gly1385=
ENST00000587391.5:c.*4015T>G	ENSP00000465525.1:n.*4015T>G
NM_001083961.1:c.4155T>G	NP_001077430.1:p.Gly1385=
NM_173636.4:c.4140T>G	NP_775907.4:p.Gly1380=
XM_005258809.2:c.4044T>G	XP_005258866.1:p.Gly1348=
XM_011526837.1:c.4140T>G	XP_011525139.1:p.Gly1380=
XM_011526838.1:c.3906T>G	XP_011525140.1:p.Gly1302=
XM_011526839.1:c.3804T>G	XP_011525141.1:p.Gly1268=
XM_011526840.1:c.3147T>G	XP_011525142.1:p.Gly1049=
XM_011526841.1:c.2733T>G	XP_011525143.1:p.Gly911=
XM_011526842.1:c.2586T>G	XP_011525144.1:p.Gly862=
XM_011526843.1:c.1902T>G	XP_011525145.1:p.Gly634=
XM_011526844.1:c.1902T>G	XP_011525146.1:p.Gly634=
XM_011526840.2:c.3147T>G	XP_011525142.1:p.Gly1049=
XM_011526841.2:c.2733T>G	XP_011525143.1:p.Gly911=
XM_011526844.2:c.1902T>G	XP_011525146.1:p.Gly634=
XM_017026665.1:c.4155T>G	XP_016882154.1:p.Gly1385=
NM_001083961.2:c.4155T>G MANE Select	NP_001077430.1:p.Gly1385=
NM_173636.5:c.4140T>G	NP_775907.4:p.Gly1380=