Canonical Allele Identifier: CA405450531

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593003A>C (hg19) ; chr19:g.36102101A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102101A>C , CM000681.2:g.36102101A>C	GRCh38
NC_000019.9:g.36593003A>C , CM000681.1:g.36593003A>C	GRCh37
NC_000019.8:g.41284843A>C	NCBI36
NG_028101.1:g.52221A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3170A>C	ENSP00000270301.6:p.Glu1057Ala
ENST00000401500.7:c.3170A>C MANE Select	ENSP00000384792.1:p.Glu1057Ala
ENST00000587391.6:c.*2445A>C	ENSP00000465525.1:n.*2445A>C
ENST00000679357.1:c.960A>C
ENST00000679422.1:c.849A>C
ENST00000679682.1:c.3155A>C	ENSP00000506226.1:p.Glu1052Ala
ENST00000679714.1:c.3164A>C	ENSP00000506627.1:p.Glu1055Ala
ENST00000679757.1:c.2819A>C	ENSP00000505158.1:p.Glu940Ala
ENST00000679858.1:c.*2552A>C	ENSP00000505655.1:n.*2552A>C
ENST00000680211.1:c.-230A>C	ENSP00000506102.1:n.-230A>C
ENST00000680349.1:n.1153A>C
ENST00000680403.1:c.3170A>C	ENSP00000505677.1:p.Glu1057Ala
ENST00000680564.1:c.2972-636A>C	ENSP00000505582.1:n.2972-636A>C
ENST00000680590.1:c.*1565A>C	ENSP00000505350.1:n.*1565A>C
ENST00000680739.1:c.88A>C
ENST00000680773.1:n.1086A>C
ENST00000680806.1:c.*1888A>C	ENSP00000506418.1:n.*1888A>C
ENST00000680997.1:n.517A>C
ENST00000681088.1:c.832A>C
ENST00000681608.1:n.118A>C
ENST00000681625.1:c.*502A>C	ENSP00000505555.1:n.*502A>C
ENST00000270301.11:c.3170A>C	ENSP00000270301.6:p.Glu1057Ala
ENST00000401500.6:c.3170A>C	ENSP00000384792.1:p.Glu1057Ala
ENST00000587391.5:c.*2445A>C	ENSP00000465525.1:n.*2445A>C
NM_001083961.1:c.3170A>C	NP_001077430.1:p.Glu1057Ala
NM_173636.4:c.3170A>C	NP_775907.4:p.Glu1057Ala
XM_005258809.2:c.3059A>C	XP_005258866.1:p.Glu1020Ala
XM_011526837.1:c.3155A>C	XP_011525139.1:p.Glu1052Ala
XM_011526838.1:c.2972-636A>C	XP_011525140.1:n.2972-636A>C
XM_011526839.1:c.2819A>C	XP_011525141.1:p.Glu940Ala
XM_011526840.1:c.2162A>C	XP_011525142.1:p.Glu721Ala
XM_011526841.1:c.1748A>C	XP_011525143.1:p.Glu583Ala
XM_011526842.1:c.1601A>C	XP_011525144.1:p.Glu534Ala
XM_011526843.1:c.917A>C	XP_011525145.1:p.Glu306Ala
XM_011526844.1:c.917A>C	XP_011525146.1:p.Glu306Ala
XM_011526840.2:c.2162A>C	XP_011525142.1:p.Glu721Ala
XM_011526841.2:c.1748A>C	XP_011525143.1:p.Glu583Ala
XM_011526844.2:c.917A>C	XP_011525146.1:p.Glu306Ala
XM_017026665.1:c.3170A>C	XP_016882154.1:p.Glu1057Ala
NM_001083961.2:c.3170A>C MANE Select	NP_001077430.1:p.Glu1057Ala
NM_173636.5:c.3170A>C	NP_775907.4:p.Glu1057Ala