Canonical Allele Identifier: CA2333970964
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102144_36102145delinsCT , CM000681.2:g.36102144_36102145delinsCT GRCh38
NC_000019.9:g.36593046_36593047delinsCT , CM000681.1:g.36593046_36593047delinsCT GRCh37
NC_000019.8:g.41284886_41284887delinsCT NCBI36
NG_028101.1:g.52264_52265delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3213_3214delinsCT ENSP00000270301.6:p.Pro1071=
ENST00000401500.7:c.3213_3214delinsCT MANE Select ENSP00000384792.1:p.Pro1071=
ENST00000587391.6:c.*2488_*2489delinsCT ENSP00000465525.1:n.*2488_*2489delinsCT
ENST00000679357.1:c.1003_1004delinsCT
ENST00000679422.1:c.892_893delinsCT
ENST00000679682.1:c.3198_3199delinsCT ENSP00000506226.1:p.Pro1066=
ENST00000679714.1:c.3207_3208delinsCT ENSP00000506627.1:p.Pro1069=
ENST00000679757.1:c.2862_2863delinsCT ENSP00000505158.1:p.Pro954=
ENST00000679858.1:c.*2595_*2596delinsCT ENSP00000505655.1:n.*2595_*2596delinsCT
ENST00000680211.1:c.-187_-186delinsCT ENSP00000506102.1:n.-187_-186delinsCT
ENST00000680349.1:n.1196_1197delinsCT
ENST00000680403.1:c.3213_3214delinsCT ENSP00000505677.1:p.Pro1071=
ENST00000680564.1:c.2972-593_2972-592delinsCT ENSP00000505582.1:n.2972-593_2972-592delinsCT
ENST00000680590.1:c.*1608_*1609delinsCT ENSP00000505350.1:n.*1608_*1609delinsCT
ENST00000680739.1:c.131_132delinsCT
ENST00000680773.1:n.1129_1130delinsCT
ENST00000680806.1:c.*1931_*1932delinsCT ENSP00000506418.1:n.*1931_*1932delinsCT
ENST00000680997.1:n.560_561delinsCT
ENST00000681088.1:c.875_876delinsCT
ENST00000681608.1:n.161_162delinsCT
ENST00000681625.1:c.*545_*546delinsCT ENSP00000505555.1:n.*545_*546delinsCT
ENST00000270301.11:c.3213_3214delinsCT ENSP00000270301.6:p.Pro1071=
ENST00000401500.6:c.3213_3214delinsCT ENSP00000384792.1:p.Pro1071=
ENST00000587391.5:c.*2488_*2489delinsCT ENSP00000465525.1:n.*2488_*2489delinsCT
NM_001083961.1:c.3213_3214delinsCT NP_001077430.1:p.Pro1071=
NM_173636.4:c.3213_3214delinsCT NP_775907.4:p.Pro1071=
XM_005258809.2:c.3102_3103delinsCT XP_005258866.1:p.Pro1034=
XM_011526837.1:c.3198_3199delinsCT XP_011525139.1:p.Pro1066=
XM_011526838.1:c.2972-593_2972-592delinsCT XP_011525140.1:n.2972-593_2972-592delinsCT
XM_011526839.1:c.2862_2863delinsCT XP_011525141.1:p.Pro954=
XM_011526840.1:c.2205_2206delinsCT XP_011525142.1:p.Pro735=
XM_011526841.1:c.1791_1792delinsCT XP_011525143.1:p.Pro597=
XM_011526842.1:c.1644_1645delinsCT XP_011525144.1:p.Pro548=
XM_011526843.1:c.960_961delinsCT XP_011525145.1:p.Pro320=
XM_011526844.1:c.960_961delinsCT XP_011525146.1:p.Pro320=
XM_011526840.2:c.2205_2206delinsCT XP_011525142.1:p.Pro735=
XM_011526841.2:c.1791_1792delinsCT XP_011525143.1:p.Pro597=
XM_011526844.2:c.960_961delinsCT XP_011525146.1:p.Pro320=
XM_017026665.1:c.3213_3214delinsCT XP_016882154.1:p.Pro1071=
NM_001083961.2:c.3213_3214delinsCT MANE Select NP_001077430.1:p.Pro1071=
NM_173636.5:c.3213_3214delinsCT NP_775907.4:p.Pro1071=