Canonical Allele Identifier: CA405450396

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592987C>G (hg19) ; chr19:g.36102085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102085C>G , CM000681.2:g.36102085C>G	GRCh38
NC_000019.9:g.36592987C>G , CM000681.1:g.36592987C>G	GRCh37
NC_000019.8:g.41284827C>G	NCBI36
NG_028101.1:g.52205C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3154C>G	ENSP00000270301.6:p.Gln1052Glu
ENST00000401500.7:c.3154C>G MANE Select	ENSP00000384792.1:p.Gln1052Glu
ENST00000587391.6:c.*2429C>G	ENSP00000465525.1:n.*2429C>G
ENST00000679357.1:c.944C>G
ENST00000679422.1:c.833C>G
ENST00000679682.1:c.3139C>G	ENSP00000506226.1:p.Gln1047Glu
ENST00000679714.1:c.3148C>G	ENSP00000506627.1:p.Gln1050Glu
ENST00000679757.1:c.2803C>G	ENSP00000505158.1:p.Gln935Glu
ENST00000679858.1:c.*2536C>G	ENSP00000505655.1:n.*2536C>G
ENST00000680211.1:c.-246C>G	ENSP00000506102.1:n.-246C>G
ENST00000680349.1:n.1137C>G
ENST00000680403.1:c.3154C>G	ENSP00000505677.1:p.Gln1052Glu
ENST00000680564.1:c.2972-652C>G	ENSP00000505582.1:n.2972-652C>G
ENST00000680590.1:c.*1549C>G	ENSP00000505350.1:n.*1549C>G
ENST00000680739.1:c.72C>G
ENST00000680773.1:n.1070C>G
ENST00000680806.1:c.*1872C>G	ENSP00000506418.1:n.*1872C>G
ENST00000680997.1:n.501C>G
ENST00000681088.1:c.816C>G
ENST00000681608.1:n.102C>G
ENST00000681625.1:c.*486C>G	ENSP00000505555.1:n.*486C>G
ENST00000270301.11:c.3154C>G	ENSP00000270301.6:p.Gln1052Glu
ENST00000401500.6:c.3154C>G	ENSP00000384792.1:p.Gln1052Glu
ENST00000587391.5:c.*2429C>G	ENSP00000465525.1:n.*2429C>G
NM_001083961.1:c.3154C>G	NP_001077430.1:p.Gln1052Glu
NM_173636.4:c.3154C>G	NP_775907.4:p.Gln1052Glu
XM_005258809.2:c.3043C>G	XP_005258866.1:p.Gln1015Glu
XM_011526837.1:c.3139C>G	XP_011525139.1:p.Gln1047Glu
XM_011526838.1:c.2972-652C>G	XP_011525140.1:n.2972-652C>G
XM_011526839.1:c.2803C>G	XP_011525141.1:p.Gln935Glu
XM_011526840.1:c.2146C>G	XP_011525142.1:p.Gln716Glu
XM_011526841.1:c.1732C>G	XP_011525143.1:p.Gln578Glu
XM_011526842.1:c.1585C>G	XP_011525144.1:p.Gln529Glu
XM_011526843.1:c.901C>G	XP_011525145.1:p.Gln301Glu
XM_011526844.1:c.901C>G	XP_011525146.1:p.Gln301Glu
XM_011526840.2:c.2146C>G	XP_011525142.1:p.Gln716Glu
XM_011526841.2:c.1732C>G	XP_011525143.1:p.Gln578Glu
XM_011526844.2:c.901C>G	XP_011525146.1:p.Gln301Glu
XM_017026665.1:c.3154C>G	XP_016882154.1:p.Gln1052Glu
NM_001083961.2:c.3154C>G MANE Select	NP_001077430.1:p.Gln1052Glu
NM_173636.5:c.3154C>G	NP_775907.4:p.Gln1052Glu