Canonical Allele Identifier: CA2333970932
Gene: WDR62 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3154C= ENSP00000270301.6:p.Gln1052=
ENST00000401500.7:c.3154C= MANE Select ENSP00000384792.1:p.Gln1052=
ENST00000587391.6:c.*2429C= ENSP00000465525.1:n.*2429C=
ENST00000679357.1:c.944C=
ENST00000679422.1:c.833C=
ENST00000679682.1:c.3139C= ENSP00000506226.1:p.Gln1047=
ENST00000679714.1:c.3148C= ENSP00000506627.1:p.Gln1050=
ENST00000679757.1:c.2803C= ENSP00000505158.1:p.Gln935=
ENST00000679858.1:c.*2536C= ENSP00000505655.1:n.*2536C=
ENST00000680211.1:c.-246C= ENSP00000506102.1:n.-246C=
ENST00000680349.1:n.1137C=
ENST00000680403.1:c.3154C= ENSP00000505677.1:p.Gln1052=
ENST00000680564.1:c.2972-652C= ENSP00000505582.1:n.2972-652C=
ENST00000680590.1:c.*1549C= ENSP00000505350.1:n.*1549C=
ENST00000680739.1:c.72C=
ENST00000680773.1:n.1070C=
ENST00000680806.1:c.*1872C= ENSP00000506418.1:n.*1872C=
ENST00000680997.1:n.501C=
ENST00000681088.1:c.816C=
ENST00000681608.1:n.102C=
ENST00000681625.1:c.*486C= ENSP00000505555.1:n.*486C=
ENST00000270301.11:c.3154C= ENSP00000270301.6:p.Gln1052=
ENST00000401500.6:c.3154C= ENSP00000384792.1:p.Gln1052=
ENST00000587391.5:c.*2429C= ENSP00000465525.1:n.*2429C=
NM_001083961.1:c.3154C= NP_001077430.1:p.Gln1052=
NM_173636.4:c.3154C= NP_775907.4:p.Gln1052=
XM_005258809.2:c.3043C= XP_005258866.1:p.Gln1015=
XM_011526837.1:c.3139C= XP_011525139.1:p.Gln1047=
XM_011526838.1:c.2972-652C= XP_011525140.1:n.2972-652C=
XM_011526839.1:c.2803C= XP_011525141.1:p.Gln935=
XM_011526840.1:c.2146C= XP_011525142.1:p.Gln716=
XM_011526841.1:c.1732C= XP_011525143.1:p.Gln578=
XM_011526842.1:c.1585C= XP_011525144.1:p.Gln529=
XM_011526843.1:c.901C= XP_011525145.1:p.Gln301=
XM_011526844.1:c.901C= XP_011525146.1:p.Gln301=
XM_011526840.2:c.2146C= XP_011525142.1:p.Gln716=
XM_011526841.2:c.1732C= XP_011525143.1:p.Gln578=
XM_011526844.2:c.901C= XP_011525146.1:p.Gln301=
XM_017026665.1:c.3154C= XP_016882154.1:p.Gln1052=
NM_001083961.2:c.3154C= MANE Select NP_001077430.1:p.Gln1052=
NM_173636.5:c.3154C= NP_775907.4:p.Gln1052=