Canonical Allele Identifier: CA405460285

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595423C>G (hg19) ; chr19:g.36104521C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104521C>G , CM000681.2:g.36104521C>G	GRCh38
NC_000019.9:g.36595423C>G , CM000681.1:g.36595423C>G	GRCh37
NC_000019.8:g.41287263C>G	NCBI36
NG_028101.1:g.54641C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4142C>G	ENSP00000270301.6:p.Ala1381Gly
ENST00000401500.7:c.4157C>G MANE Select	ENSP00000384792.1:p.Ala1386Gly
ENST00000587391.6:c.*4017C>G	ENSP00000465525.1:n.*4017C>G
ENST00000679357.1:c.2237C>G
ENST00000679598.1:c.919-17C>G
ENST00000679682.1:c.4142C>G	ENSP00000506226.1:p.Ala1381Gly
ENST00000679714.1:c.4151C>G	ENSP00000506627.1:p.Ala1384Gly
ENST00000679757.1:c.3806C>G	ENSP00000505158.1:p.Ala1269Gly
ENST00000679858.1:c.*3539C>G	ENSP00000505655.1:n.*3539C>G
ENST00000680211.1:c.758C>G	ENSP00000506102.1:p.Ala253Gly
ENST00000680280.1:n.1660C>G
ENST00000680349.1:n.2806C>G
ENST00000680403.1:c.4142C>G	ENSP00000505677.1:p.Ala1381Gly
ENST00000680564.1:c.3908C>G	ENSP00000505582.1:p.Ala1303Gly
ENST00000680590.1:c.*2537C>G	ENSP00000505350.1:n.*2537C>G
ENST00000680597.1:c.890C>G
ENST00000680739.1:c.1172C>G
ENST00000680773.1:n.2658C>G
ENST00000680806.1:c.*3460C>G	ENSP00000506418.1:n.*3460C>G
ENST00000680997.1:n.2089C>G
ENST00000681608.1:n.2002C>G
ENST00000681625.1:c.*1489C>G	ENSP00000505555.1:n.*1489C>G
ENST00000681648.1:n.2208C>G
ENST00000270301.11:c.4142C>G	ENSP00000270301.6:p.Ala1381Gly
ENST00000401500.6:c.4157C>G	ENSP00000384792.1:p.Ala1386Gly
ENST00000587391.5:c.*4017C>G	ENSP00000465525.1:n.*4017C>G
NM_001083961.1:c.4157C>G	NP_001077430.1:p.Ala1386Gly
NM_173636.4:c.4142C>G	NP_775907.4:p.Ala1381Gly
XM_005258809.2:c.4046C>G	XP_005258866.1:p.Ala1349Gly
XM_011526837.1:c.4142C>G	XP_011525139.1:p.Ala1381Gly
XM_011526838.1:c.3908C>G	XP_011525140.1:p.Ala1303Gly
XM_011526839.1:c.3806C>G	XP_011525141.1:p.Ala1269Gly
XM_011526840.1:c.3149C>G	XP_011525142.1:p.Ala1050Gly
XM_011526841.1:c.2735C>G	XP_011525143.1:p.Ala912Gly
XM_011526842.1:c.2588C>G	XP_011525144.1:p.Ala863Gly
XM_011526843.1:c.1904C>G	XP_011525145.1:p.Ala635Gly
XM_011526844.1:c.1904C>G	XP_011525146.1:p.Ala635Gly
XM_011526840.2:c.3149C>G	XP_011525142.1:p.Ala1050Gly
XM_011526841.2:c.2735C>G	XP_011525143.1:p.Ala912Gly
XM_011526844.2:c.1904C>G	XP_011525146.1:p.Ala635Gly
XM_017026665.1:c.4157C>G	XP_016882154.1:p.Ala1386Gly
NM_001083961.2:c.4157C>G MANE Select	NP_001077430.1:p.Ala1386Gly
NM_173636.5:c.4142C>G	NP_775907.4:p.Ala1381Gly