Canonical Allele Identifier: CA2333970907
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102035A= , CM000681.2:g.36102035A= GRCh38
NC_000019.9:g.36592937A= , CM000681.1:g.36592937A= GRCh37
NC_000019.8:g.41284777A= NCBI36
NG_028101.1:g.52155A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3104A= ENSP00000270301.6:p.Asp1035=
ENST00000401500.7:c.3104A= MANE Select ENSP00000384792.1:p.Asp1035=
ENST00000587391.6:c.*2379A= ENSP00000465525.1:n.*2379A=
ENST00000679357.1:c.894A=
ENST00000679422.1:c.783A=
ENST00000679682.1:c.3089A= ENSP00000506226.1:p.Asp1030=
ENST00000679714.1:c.3098A= ENSP00000506627.1:p.Asp1033=
ENST00000679757.1:c.2753A= ENSP00000505158.1:p.Asp918=
ENST00000679858.1:c.*2486A= ENSP00000505655.1:n.*2486A=
ENST00000680211.1:c.-296A= ENSP00000506102.1:n.-296A=
ENST00000680349.1:n.1087A=
ENST00000680403.1:c.3104A= ENSP00000505677.1:p.Asp1035=
ENST00000680564.1:c.2972-702A= ENSP00000505582.1:n.2972-702A=
ENST00000680590.1:c.*1499A= ENSP00000505350.1:n.*1499A=
ENST00000680739.1:c.22A=
ENST00000680773.1:n.1020A=
ENST00000680806.1:c.*1822A= ENSP00000506418.1:n.*1822A=
ENST00000680997.1:n.451A=
ENST00000681088.1:c.766A=
ENST00000681608.1:n.52A=
ENST00000681625.1:c.*436A= ENSP00000505555.1:n.*436A=
ENST00000270301.11:c.3104A= ENSP00000270301.6:p.Asp1035=
ENST00000401500.6:c.3104A= ENSP00000384792.1:p.Asp1035=
ENST00000587391.5:c.*2379A= ENSP00000465525.1:n.*2379A=
NM_001083961.1:c.3104A= NP_001077430.1:p.Asp1035=
NM_173636.4:c.3104A= NP_775907.4:p.Asp1035=
XM_005258809.2:c.2993A= XP_005258866.1:p.Asp998=
XM_011526837.1:c.3089A= XP_011525139.1:p.Asp1030=
XM_011526838.1:c.2972-702A= XP_011525140.1:n.2972-702A=
XM_011526839.1:c.2753A= XP_011525141.1:p.Asp918=
XM_011526840.1:c.2096A= XP_011525142.1:p.Asp699=
XM_011526841.1:c.1682A= XP_011525143.1:p.Asp561=
XM_011526842.1:c.1535A= XP_011525144.1:p.Asp512=
XM_011526843.1:c.851A= XP_011525145.1:p.Asp284=
XM_011526844.1:c.851A= XP_011525146.1:p.Asp284=
XM_011526840.2:c.2096A= XP_011525142.1:p.Asp699=
XM_011526841.2:c.1682A= XP_011525143.1:p.Asp561=
XM_011526844.2:c.851A= XP_011525146.1:p.Asp284=
XM_017026665.1:c.3104A= XP_016882154.1:p.Asp1035=
NM_001083961.2:c.3104A= MANE Select NP_001077430.1:p.Asp1035=
NM_173636.5:c.3104A= NP_775907.4:p.Asp1035=