Canonical Allele Identifier: CA2333970917
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102057A= , CM000681.2:g.36102057A= GRCh38
NC_000019.9:g.36592959A= , CM000681.1:g.36592959A= GRCh37
NC_000019.8:g.41284799A= NCBI36
NG_028101.1:g.52177A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3126A= ENSP00000270301.6:p.Gly1042=
ENST00000401500.7:c.3126A= MANE Select ENSP00000384792.1:p.Gly1042=
ENST00000587391.6:c.*2401A= ENSP00000465525.1:n.*2401A=
ENST00000679357.1:c.916A=
ENST00000679422.1:c.805A=
ENST00000679682.1:c.3111A= ENSP00000506226.1:p.Gly1037=
ENST00000679714.1:c.3120A= ENSP00000506627.1:p.Gly1040=
ENST00000679757.1:c.2775A= ENSP00000505158.1:p.Gly925=
ENST00000679858.1:c.*2508A= ENSP00000505655.1:n.*2508A=
ENST00000680211.1:c.-274A= ENSP00000506102.1:n.-274A=
ENST00000680349.1:n.1109A=
ENST00000680403.1:c.3126A= ENSP00000505677.1:p.Gly1042=
ENST00000680564.1:c.2972-680A= ENSP00000505582.1:n.2972-680A=
ENST00000680590.1:c.*1521A= ENSP00000505350.1:n.*1521A=
ENST00000680739.1:c.44A=
ENST00000680773.1:n.1042A=
ENST00000680806.1:c.*1844A= ENSP00000506418.1:n.*1844A=
ENST00000680997.1:n.473A=
ENST00000681088.1:c.788A=
ENST00000681608.1:n.74A=
ENST00000681625.1:c.*458A= ENSP00000505555.1:n.*458A=
ENST00000270301.11:c.3126A= ENSP00000270301.6:p.Gly1042=
ENST00000401500.6:c.3126A= ENSP00000384792.1:p.Gly1042=
ENST00000587391.5:c.*2401A= ENSP00000465525.1:n.*2401A=
NM_001083961.1:c.3126A= NP_001077430.1:p.Gly1042=
NM_173636.4:c.3126A= NP_775907.4:p.Gly1042=
XM_005258809.2:c.3015A= XP_005258866.1:p.Gly1005=
XM_011526837.1:c.3111A= XP_011525139.1:p.Gly1037=
XM_011526838.1:c.2972-680A= XP_011525140.1:n.2972-680A=
XM_011526839.1:c.2775A= XP_011525141.1:p.Gly925=
XM_011526840.1:c.2118A= XP_011525142.1:p.Gly706=
XM_011526841.1:c.1704A= XP_011525143.1:p.Gly568=
XM_011526842.1:c.1557A= XP_011525144.1:p.Gly519=
XM_011526843.1:c.873A= XP_011525145.1:p.Gly291=
XM_011526844.1:c.873A= XP_011525146.1:p.Gly291=
XM_011526840.2:c.2118A= XP_011525142.1:p.Gly706=
XM_011526841.2:c.1704A= XP_011525143.1:p.Gly568=
XM_011526844.2:c.873A= XP_011525146.1:p.Gly291=
XM_017026665.1:c.3126A= XP_016882154.1:p.Gly1042=
NM_001083961.2:c.3126A= MANE Select NP_001077430.1:p.Gly1042=
NM_173636.5:c.3126A= NP_775907.4:p.Gly1042=