Canonical Allele Identifier: CA2333970934
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102088A= , CM000681.2:g.36102088A= GRCh38
NC_000019.9:g.36592990A= , CM000681.1:g.36592990A= GRCh37
NC_000019.8:g.41284830A= NCBI36
NG_028101.1:g.52208A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3157A= ENSP00000270301.6:p.Thr1053=
ENST00000401500.7:c.3157A= MANE Select ENSP00000384792.1:p.Thr1053=
ENST00000587391.6:c.*2432A= ENSP00000465525.1:n.*2432A=
ENST00000679357.1:c.947A=
ENST00000679422.1:c.836A=
ENST00000679682.1:c.3142A= ENSP00000506226.1:p.Thr1048=
ENST00000679714.1:c.3151A= ENSP00000506627.1:p.Thr1051=
ENST00000679757.1:c.2806A= ENSP00000505158.1:p.Thr936=
ENST00000679858.1:c.*2539A= ENSP00000505655.1:n.*2539A=
ENST00000680211.1:c.-243A= ENSP00000506102.1:n.-243A=
ENST00000680349.1:n.1140A=
ENST00000680403.1:c.3157A= ENSP00000505677.1:p.Thr1053=
ENST00000680564.1:c.2972-649A= ENSP00000505582.1:n.2972-649A=
ENST00000680590.1:c.*1552A= ENSP00000505350.1:n.*1552A=
ENST00000680739.1:c.75A=
ENST00000680773.1:n.1073A=
ENST00000680806.1:c.*1875A= ENSP00000506418.1:n.*1875A=
ENST00000680997.1:n.504A=
ENST00000681088.1:c.819A=
ENST00000681608.1:n.105A=
ENST00000681625.1:c.*489A= ENSP00000505555.1:n.*489A=
ENST00000270301.11:c.3157A= ENSP00000270301.6:p.Thr1053=
ENST00000401500.6:c.3157A= ENSP00000384792.1:p.Thr1053=
ENST00000587391.5:c.*2432A= ENSP00000465525.1:n.*2432A=
NM_001083961.1:c.3157A= NP_001077430.1:p.Thr1053=
NM_173636.4:c.3157A= NP_775907.4:p.Thr1053=
XM_005258809.2:c.3046A= XP_005258866.1:p.Thr1016=
XM_011526837.1:c.3142A= XP_011525139.1:p.Thr1048=
XM_011526838.1:c.2972-649A= XP_011525140.1:n.2972-649A=
XM_011526839.1:c.2806A= XP_011525141.1:p.Thr936=
XM_011526840.1:c.2149A= XP_011525142.1:p.Thr717=
XM_011526841.1:c.1735A= XP_011525143.1:p.Thr579=
XM_011526842.1:c.1588A= XP_011525144.1:p.Thr530=
XM_011526843.1:c.904A= XP_011525145.1:p.Thr302=
XM_011526844.1:c.904A= XP_011525146.1:p.Thr302=
XM_011526840.2:c.2149A= XP_011525142.1:p.Thr717=
XM_011526841.2:c.1735A= XP_011525143.1:p.Thr579=
XM_011526844.2:c.904A= XP_011525146.1:p.Thr302=
XM_017026665.1:c.3157A= XP_016882154.1:p.Thr1053=
NM_001083961.2:c.3157A= MANE Select NP_001077430.1:p.Thr1053=
NM_173636.5:c.3157A= NP_775907.4:p.Thr1053=