Canonical Allele Identifier: CA2333971290
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102777A= , CM000681.2:g.36102777A= GRCh38
NC_000019.9:g.36593679A= , CM000681.1:g.36593679A= GRCh37
NC_000019.8:g.41285519A= NCBI36
NG_028101.1:g.52897A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3246A= ENSP00000270301.6:p.Glu1082=
ENST00000401500.7:c.3261A= MANE Select ENSP00000384792.1:p.Glu1087=
ENST00000587391.6:c.*3121A= ENSP00000465525.1:n.*3121A=
ENST00000679357.1:c.1341A=
ENST00000679598.1:c.26A=
ENST00000679682.1:c.3246A= ENSP00000506226.1:p.Glu1082=
ENST00000679714.1:c.3255A= ENSP00000506627.1:p.Glu1085=
ENST00000679757.1:c.2910A= ENSP00000505158.1:p.Glu970=
ENST00000679858.1:c.*2643A= ENSP00000505655.1:n.*2643A=
ENST00000680211.1:c.-139A= ENSP00000506102.1:n.-139A=
ENST00000680280.1:n.548A=
ENST00000680349.1:n.1829A=
ENST00000680403.1:c.3246A= ENSP00000505677.1:p.Glu1082=
ENST00000680564.1:c.3012A= ENSP00000505582.1:p.Glu1004=
ENST00000680590.1:c.*1641A= ENSP00000505350.1:n.*1641A=
ENST00000680597.1:c.26A=
ENST00000680739.1:c.276A=
ENST00000680773.1:n.1762A=
ENST00000680806.1:c.*2564A= ENSP00000506418.1:n.*2564A=
ENST00000680997.1:n.1193A=
ENST00000681608.1:n.794A=
ENST00000681625.1:c.*593A= ENSP00000505555.1:n.*593A=
ENST00000681648.1:n.560A=
ENST00000270301.11:c.3246A= ENSP00000270301.6:p.Glu1082=
ENST00000401500.6:c.3261A= ENSP00000384792.1:p.Glu1087=
ENST00000587391.5:c.*3121A= ENSP00000465525.1:n.*3121A=
NM_001083961.1:c.3261A= NP_001077430.1:p.Glu1087=
NM_173636.4:c.3246A= NP_775907.4:p.Glu1082=
XM_005258809.2:c.3150A= XP_005258866.1:p.Glu1050=
XM_011526837.1:c.3246A= XP_011525139.1:p.Glu1082=
XM_011526838.1:c.3012A= XP_011525140.1:p.Glu1004=
XM_011526839.1:c.2910A= XP_011525141.1:p.Glu970=
XM_011526840.1:c.2253A= XP_011525142.1:p.Glu751=
XM_011526841.1:c.1839A= XP_011525143.1:p.Glu613=
XM_011526842.1:c.1692A= XP_011525144.1:p.Glu564=
XM_011526843.1:c.1008A= XP_011525145.1:p.Glu336=
XM_011526844.1:c.1008A= XP_011525146.1:p.Glu336=
XM_011526840.2:c.2253A= XP_011525142.1:p.Glu751=
XM_011526841.2:c.1839A= XP_011525143.1:p.Glu613=
XM_011526844.2:c.1008A= XP_011525146.1:p.Glu336=
XM_017026665.1:c.3261A= XP_016882154.1:p.Glu1087=
NM_001083961.2:c.3261A= MANE Select NP_001077430.1:p.Glu1087=
NM_173636.5:c.3246A= NP_775907.4:p.Glu1082=