Canonical Allele Identifier: CA405460505

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595463G>C (hg19) ; chr19:g.36104561G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104561G>C , CM000681.2:g.36104561G>C	GRCh38
NC_000019.9:g.36595463G>C , CM000681.1:g.36595463G>C	GRCh37
NC_000019.8:g.41287303G>C	NCBI36
NG_028101.1:g.54681G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4182G>C	ENSP00000270301.6:p.Glu1394Asp
ENST00000401500.7:c.4197G>C MANE Select	ENSP00000384792.1:p.Glu1399Asp
ENST00000587391.6:c.*4057G>C	ENSP00000465525.1:n.*4057G>C
ENST00000679357.1:c.2277G>C
ENST00000679598.1:c.942G>C
ENST00000679682.1:c.4182G>C	ENSP00000506226.1:p.Glu1394Asp
ENST00000679714.1:c.4191G>C	ENSP00000506627.1:p.Glu1397Asp
ENST00000679757.1:c.3846G>C	ENSP00000505158.1:p.Glu1282Asp
ENST00000679858.1:c.*3579G>C	ENSP00000505655.1:n.*3579G>C
ENST00000680211.1:c.798G>C	ENSP00000506102.1:p.Glu266Asp
ENST00000680280.1:n.1700G>C
ENST00000680349.1:n.2846G>C
ENST00000680403.1:c.4182G>C	ENSP00000505677.1:p.Glu1394Asp
ENST00000680564.1:c.3948G>C	ENSP00000505582.1:p.Glu1316Asp
ENST00000680590.1:c.*2577G>C	ENSP00000505350.1:n.*2577G>C
ENST00000680597.1:c.930G>C
ENST00000680739.1:c.1212G>C
ENST00000680773.1:n.2698G>C
ENST00000680806.1:c.*3500G>C	ENSP00000506418.1:n.*3500G>C
ENST00000680997.1:n.2129G>C
ENST00000681608.1:n.2042G>C
ENST00000681625.1:c.*1529G>C	ENSP00000505555.1:n.*1529G>C
ENST00000681648.1:n.2248G>C
ENST00000270301.11:c.4182G>C	ENSP00000270301.6:p.Glu1394Asp
ENST00000401500.6:c.4197G>C	ENSP00000384792.1:p.Glu1399Asp
ENST00000587391.5:c.*4057G>C	ENSP00000465525.1:n.*4057G>C
NM_001083961.1:c.4197G>C	NP_001077430.1:p.Glu1399Asp
NM_173636.4:c.4182G>C	NP_775907.4:p.Glu1394Asp
XM_005258809.2:c.4086G>C	XP_005258866.1:p.Glu1362Asp
XM_011526837.1:c.4182G>C	XP_011525139.1:p.Glu1394Asp
XM_011526838.1:c.3948G>C	XP_011525140.1:p.Glu1316Asp
XM_011526839.1:c.3846G>C	XP_011525141.1:p.Glu1282Asp
XM_011526840.1:c.3189G>C	XP_011525142.1:p.Glu1063Asp
XM_011526841.1:c.2775G>C	XP_011525143.1:p.Glu925Asp
XM_011526842.1:c.2628G>C	XP_011525144.1:p.Glu876Asp
XM_011526843.1:c.1944G>C	XP_011525145.1:p.Glu648Asp
XM_011526844.1:c.1944G>C	XP_011525146.1:p.Glu648Asp
XM_011526840.2:c.3189G>C	XP_011525142.1:p.Glu1063Asp
XM_011526841.2:c.2775G>C	XP_011525143.1:p.Glu925Asp
XM_011526844.2:c.1944G>C	XP_011525146.1:p.Glu648Asp
XM_017026665.1:c.4197G>C	XP_016882154.1:p.Glu1399Asp
NM_001083961.2:c.4197G>C MANE Select	NP_001077430.1:p.Glu1399Asp
NM_173636.5:c.4182G>C	NP_775907.4:p.Glu1394Asp