Canonical Allele Identifier: CA2333970939
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102095A= , CM000681.2:g.36102095A= GRCh38
NC_000019.9:g.36592997A= , CM000681.1:g.36592997A= GRCh37
NC_000019.8:g.41284837A= NCBI36
NG_028101.1:g.52215A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3164A= ENSP00000270301.6:p.Glu1055=
ENST00000401500.7:c.3164A= MANE Select ENSP00000384792.1:p.Glu1055=
ENST00000587391.6:c.*2439A= ENSP00000465525.1:n.*2439A=
ENST00000679357.1:c.954A=
ENST00000679422.1:c.843A=
ENST00000679682.1:c.3149A= ENSP00000506226.1:p.Glu1050=
ENST00000679714.1:c.3158A= ENSP00000506627.1:p.Glu1053=
ENST00000679757.1:c.2813A= ENSP00000505158.1:p.Glu938=
ENST00000679858.1:c.*2546A= ENSP00000505655.1:n.*2546A=
ENST00000680211.1:c.-236A= ENSP00000506102.1:n.-236A=
ENST00000680349.1:n.1147A=
ENST00000680403.1:c.3164A= ENSP00000505677.1:p.Glu1055=
ENST00000680564.1:c.2972-642A= ENSP00000505582.1:n.2972-642A=
ENST00000680590.1:c.*1559A= ENSP00000505350.1:n.*1559A=
ENST00000680739.1:c.82A=
ENST00000680773.1:n.1080A=
ENST00000680806.1:c.*1882A= ENSP00000506418.1:n.*1882A=
ENST00000680997.1:n.511A=
ENST00000681088.1:c.826A=
ENST00000681608.1:n.112A=
ENST00000681625.1:c.*496A= ENSP00000505555.1:n.*496A=
ENST00000270301.11:c.3164A= ENSP00000270301.6:p.Glu1055=
ENST00000401500.6:c.3164A= ENSP00000384792.1:p.Glu1055=
ENST00000587391.5:c.*2439A= ENSP00000465525.1:n.*2439A=
NM_001083961.1:c.3164A= NP_001077430.1:p.Glu1055=
NM_173636.4:c.3164A= NP_775907.4:p.Glu1055=
XM_005258809.2:c.3053A= XP_005258866.1:p.Glu1018=
XM_011526837.1:c.3149A= XP_011525139.1:p.Glu1050=
XM_011526838.1:c.2972-642A= XP_011525140.1:n.2972-642A=
XM_011526839.1:c.2813A= XP_011525141.1:p.Glu938=
XM_011526840.1:c.2156A= XP_011525142.1:p.Glu719=
XM_011526841.1:c.1742A= XP_011525143.1:p.Glu581=
XM_011526842.1:c.1595A= XP_011525144.1:p.Glu532=
XM_011526843.1:c.911A= XP_011525145.1:p.Glu304=
XM_011526844.1:c.911A= XP_011525146.1:p.Glu304=
XM_011526840.2:c.2156A= XP_011525142.1:p.Glu719=
XM_011526841.2:c.1742A= XP_011525143.1:p.Glu581=
XM_011526844.2:c.911A= XP_011525146.1:p.Glu304=
XM_017026665.1:c.3164A= XP_016882154.1:p.Glu1055=
NM_001083961.2:c.3164A= MANE Select NP_001077430.1:p.Glu1055=
NM_173636.5:c.3164A= NP_775907.4:p.Glu1055=