Canonical Allele Identifier: CA405460315

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595429G>A (hg19) ; chr19:g.36104527G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104527G>A , CM000681.2:g.36104527G>A	GRCh38
NC_000019.9:g.36595429G>A , CM000681.1:g.36595429G>A	GRCh37
NC_000019.8:g.41287269G>A	NCBI36
NG_028101.1:g.54647G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4148G>A	ENSP00000270301.6:p.Gly1383Asp
ENST00000401500.7:c.4163G>A MANE Select	ENSP00000384792.1:p.Gly1388Asp
ENST00000587391.6:c.*4023G>A	ENSP00000465525.1:n.*4023G>A
ENST00000679357.1:c.2243G>A
ENST00000679598.1:c.919-11G>A
ENST00000679682.1:c.4148G>A	ENSP00000506226.1:p.Gly1383Asp
ENST00000679714.1:c.4157G>A	ENSP00000506627.1:p.Gly1386Asp
ENST00000679757.1:c.3812G>A	ENSP00000505158.1:p.Gly1271Asp
ENST00000679858.1:c.*3545G>A	ENSP00000505655.1:n.*3545G>A
ENST00000680211.1:c.764G>A	ENSP00000506102.1:p.Gly255Asp
ENST00000680280.1:n.1666G>A
ENST00000680349.1:n.2812G>A
ENST00000680403.1:c.4148G>A	ENSP00000505677.1:p.Gly1383Asp
ENST00000680564.1:c.3914G>A	ENSP00000505582.1:p.Gly1305Asp
ENST00000680590.1:c.*2543G>A	ENSP00000505350.1:n.*2543G>A
ENST00000680597.1:c.896G>A
ENST00000680739.1:c.1178G>A
ENST00000680773.1:n.2664G>A
ENST00000680806.1:c.*3466G>A	ENSP00000506418.1:n.*3466G>A
ENST00000680997.1:n.2095G>A
ENST00000681608.1:n.2008G>A
ENST00000681625.1:c.*1495G>A	ENSP00000505555.1:n.*1495G>A
ENST00000681648.1:n.2214G>A
ENST00000270301.11:c.4148G>A	ENSP00000270301.6:p.Gly1383Asp
ENST00000401500.6:c.4163G>A	ENSP00000384792.1:p.Gly1388Asp
ENST00000587391.5:c.*4023G>A	ENSP00000465525.1:n.*4023G>A
NM_001083961.1:c.4163G>A	NP_001077430.1:p.Gly1388Asp
NM_173636.4:c.4148G>A	NP_775907.4:p.Gly1383Asp
XM_005258809.2:c.4052G>A	XP_005258866.1:p.Gly1351Asp
XM_011526837.1:c.4148G>A	XP_011525139.1:p.Gly1383Asp
XM_011526838.1:c.3914G>A	XP_011525140.1:p.Gly1305Asp
XM_011526839.1:c.3812G>A	XP_011525141.1:p.Gly1271Asp
XM_011526840.1:c.3155G>A	XP_011525142.1:p.Gly1052Asp
XM_011526841.1:c.2741G>A	XP_011525143.1:p.Gly914Asp
XM_011526842.1:c.2594G>A	XP_011525144.1:p.Gly865Asp
XM_011526843.1:c.1910G>A	XP_011525145.1:p.Gly637Asp
XM_011526844.1:c.1910G>A	XP_011525146.1:p.Gly637Asp
XM_011526840.2:c.3155G>A	XP_011525142.1:p.Gly1052Asp
XM_011526841.2:c.2741G>A	XP_011525143.1:p.Gly914Asp
XM_011526844.2:c.1910G>A	XP_011525146.1:p.Gly637Asp
XM_017026665.1:c.4163G>A	XP_016882154.1:p.Gly1388Asp
NM_001083961.2:c.4163G>A MANE Select	NP_001077430.1:p.Gly1388Asp
NM_173636.5:c.4148G>A	NP_775907.4:p.Gly1383Asp