Canonical Allele Identifier: CA405450848

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593040G>C (hg19) ; chr19:g.36102138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102138G>C , CM000681.2:g.36102138G>C	GRCh38
NC_000019.9:g.36593040G>C , CM000681.1:g.36593040G>C	GRCh37
NC_000019.8:g.41284880G>C	NCBI36
NG_028101.1:g.52258G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3207G>C	ENSP00000270301.6:p.Glu1069Asp
ENST00000401500.7:c.3207G>C MANE Select	ENSP00000384792.1:p.Glu1069Asp
ENST00000587391.6:c.*2482G>C	ENSP00000465525.1:n.*2482G>C
ENST00000679357.1:c.997G>C
ENST00000679422.1:c.886G>C
ENST00000679682.1:c.3192G>C	ENSP00000506226.1:p.Glu1064Asp
ENST00000679714.1:c.3201G>C	ENSP00000506627.1:p.Glu1067Asp
ENST00000679757.1:c.2856G>C	ENSP00000505158.1:p.Glu952Asp
ENST00000679858.1:c.*2589G>C	ENSP00000505655.1:n.*2589G>C
ENST00000680211.1:c.-193G>C	ENSP00000506102.1:n.-193G>C
ENST00000680349.1:n.1190G>C
ENST00000680403.1:c.3207G>C	ENSP00000505677.1:p.Glu1069Asp
ENST00000680564.1:c.2972-599G>C	ENSP00000505582.1:n.2972-599G>C
ENST00000680590.1:c.*1602G>C	ENSP00000505350.1:n.*1602G>C
ENST00000680739.1:c.125G>C
ENST00000680773.1:n.1123G>C
ENST00000680806.1:c.*1925G>C	ENSP00000506418.1:n.*1925G>C
ENST00000680997.1:n.554G>C
ENST00000681088.1:c.869G>C
ENST00000681608.1:n.155G>C
ENST00000681625.1:c.*539G>C	ENSP00000505555.1:n.*539G>C
ENST00000270301.11:c.3207G>C	ENSP00000270301.6:p.Glu1069Asp
ENST00000401500.6:c.3207G>C	ENSP00000384792.1:p.Glu1069Asp
ENST00000587391.5:c.*2482G>C	ENSP00000465525.1:n.*2482G>C
NM_001083961.1:c.3207G>C	NP_001077430.1:p.Glu1069Asp
NM_173636.4:c.3207G>C	NP_775907.4:p.Glu1069Asp
XM_005258809.2:c.3096G>C	XP_005258866.1:p.Glu1032Asp
XM_011526837.1:c.3192G>C	XP_011525139.1:p.Glu1064Asp
XM_011526838.1:c.2972-599G>C	XP_011525140.1:n.2972-599G>C
XM_011526839.1:c.2856G>C	XP_011525141.1:p.Glu952Asp
XM_011526840.1:c.2199G>C	XP_011525142.1:p.Glu733Asp
XM_011526841.1:c.1785G>C	XP_011525143.1:p.Glu595Asp
XM_011526842.1:c.1638G>C	XP_011525144.1:p.Glu546Asp
XM_011526843.1:c.954G>C	XP_011525145.1:p.Glu318Asp
XM_011526844.1:c.954G>C	XP_011525146.1:p.Glu318Asp
XM_011526840.2:c.2199G>C	XP_011525142.1:p.Glu733Asp
XM_011526841.2:c.1785G>C	XP_011525143.1:p.Glu595Asp
XM_011526844.2:c.954G>C	XP_011525146.1:p.Glu318Asp
XM_017026665.1:c.3207G>C	XP_016882154.1:p.Glu1069Asp
NM_001083961.2:c.3207G>C MANE Select	NP_001077430.1:p.Glu1069Asp
NM_173636.5:c.3207G>C	NP_775907.4:p.Glu1069Asp