Canonical Allele Identifier: CA405460311

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595428G>T (hg19) ; chr19:g.36104526G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104526G>T , CM000681.2:g.36104526G>T	GRCh38
NC_000019.9:g.36595428G>T , CM000681.1:g.36595428G>T	GRCh37
NC_000019.8:g.41287268G>T	NCBI36
NG_028101.1:g.54646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4147G>T	ENSP00000270301.6:p.Gly1383Cys
ENST00000401500.7:c.4162G>T MANE Select	ENSP00000384792.1:p.Gly1388Cys
ENST00000587391.6:c.*4022G>T	ENSP00000465525.1:n.*4022G>T
ENST00000679357.1:c.2242G>T
ENST00000679598.1:c.919-12G>T
ENST00000679682.1:c.4147G>T	ENSP00000506226.1:p.Gly1383Cys
ENST00000679714.1:c.4156G>T	ENSP00000506627.1:p.Gly1386Cys
ENST00000679757.1:c.3811G>T	ENSP00000505158.1:p.Gly1271Cys
ENST00000679858.1:c.*3544G>T	ENSP00000505655.1:n.*3544G>T
ENST00000680211.1:c.763G>T	ENSP00000506102.1:p.Gly255Cys
ENST00000680280.1:n.1665G>T
ENST00000680349.1:n.2811G>T
ENST00000680403.1:c.4147G>T	ENSP00000505677.1:p.Gly1383Cys
ENST00000680564.1:c.3913G>T	ENSP00000505582.1:p.Gly1305Cys
ENST00000680590.1:c.*2542G>T	ENSP00000505350.1:n.*2542G>T
ENST00000680597.1:c.895G>T
ENST00000680739.1:c.1177G>T
ENST00000680773.1:n.2663G>T
ENST00000680806.1:c.*3465G>T	ENSP00000506418.1:n.*3465G>T
ENST00000680997.1:n.2094G>T
ENST00000681608.1:n.2007G>T
ENST00000681625.1:c.*1494G>T	ENSP00000505555.1:n.*1494G>T
ENST00000681648.1:n.2213G>T
ENST00000270301.11:c.4147G>T	ENSP00000270301.6:p.Gly1383Cys
ENST00000401500.6:c.4162G>T	ENSP00000384792.1:p.Gly1388Cys
ENST00000587391.5:c.*4022G>T	ENSP00000465525.1:n.*4022G>T
NM_001083961.1:c.4162G>T	NP_001077430.1:p.Gly1388Cys
NM_173636.4:c.4147G>T	NP_775907.4:p.Gly1383Cys
XM_005258809.2:c.4051G>T	XP_005258866.1:p.Gly1351Cys
XM_011526837.1:c.4147G>T	XP_011525139.1:p.Gly1383Cys
XM_011526838.1:c.3913G>T	XP_011525140.1:p.Gly1305Cys
XM_011526839.1:c.3811G>T	XP_011525141.1:p.Gly1271Cys
XM_011526840.1:c.3154G>T	XP_011525142.1:p.Gly1052Cys
XM_011526841.1:c.2740G>T	XP_011525143.1:p.Gly914Cys
XM_011526842.1:c.2593G>T	XP_011525144.1:p.Gly865Cys
XM_011526843.1:c.1909G>T	XP_011525145.1:p.Gly637Cys
XM_011526844.1:c.1909G>T	XP_011525146.1:p.Gly637Cys
XM_011526840.2:c.3154G>T	XP_011525142.1:p.Gly1052Cys
XM_011526841.2:c.2740G>T	XP_011525143.1:p.Gly914Cys
XM_011526844.2:c.1909G>T	XP_011525146.1:p.Gly637Cys
XM_017026665.1:c.4162G>T	XP_016882154.1:p.Gly1388Cys
NM_001083961.2:c.4162G>T MANE Select	NP_001077430.1:p.Gly1388Cys
NM_173636.5:c.4147G>T	NP_775907.4:p.Gly1383Cys