Canonical Allele Identifier: CA2499225458
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36103162_36103163del , CM000681.2:g.36103162_36103163del GRCh38
NC_000019.9:g.36594064_36594065del , CM000681.1:g.36594064_36594065del GRCh37
NC_000019.8:g.41285904_41285905del NCBI36
NG_028101.1:g.53282_53283del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3454_3455del ENSP00000270301.6:p.Ala1152CysfsTer5
ENST00000401500.7:c.3469_3470del MANE Select ENSP00000384792.1:p.Ala1157CysfsTer5
ENST00000587391.6:c.*3329_*3330del ENSP00000465525.1:n.*3329_*3330del
ENST00000679357.1:c.1549_1550del
ENST00000679598.1:c.234_235del
ENST00000679682.1:c.3454_3455del ENSP00000506226.1:p.Ala1152CysfsTer5
ENST00000679714.1:c.3463_3464del ENSP00000506627.1:p.Ala1155CysfsTer5
ENST00000679757.1:c.3118_3119del ENSP00000505158.1:p.Ala1040CysfsTer5
ENST00000679858.1:c.*2851_*2852del ENSP00000505655.1:n.*2851_*2852del
ENST00000680211.1:c.70_71del ENSP00000506102.1:p.Ala24CysfsTer5
ENST00000680280.1:n.837_838del
ENST00000680349.1:n.2118_2119del
ENST00000680403.1:c.3454_3455del ENSP00000505677.1:p.Ala1152CysfsTer5
ENST00000680564.1:c.3220_3221del ENSP00000505582.1:p.Ala1074CysfsTer5
ENST00000680590.1:c.*1849_*1850del ENSP00000505350.1:n.*1849_*1850del
ENST00000680597.1:c.202_203del
ENST00000680739.1:c.484_485del
ENST00000680773.1:n.1970_1971del
ENST00000680806.1:c.*2772_*2773del ENSP00000506418.1:n.*2772_*2773del
ENST00000680997.1:n.1401_1402del
ENST00000681608.1:n.1179_1180del
ENST00000681625.1:c.*801_*802del ENSP00000505555.1:n.*801_*802del
ENST00000681648.1:n.849_850del
ENST00000270301.11:c.3454_3455del ENSP00000270301.6:p.Ala1152CysfsTer5
ENST00000401500.6:c.3469_3470del ENSP00000384792.1:p.Ala1157CysfsTer5
ENST00000587391.5:c.*3329_*3330del ENSP00000465525.1:n.*3329_*3330del
NM_001083961.1:c.3469_3470del NP_001077430.1:p.Ala1157CysfsTer5
NM_173636.4:c.3454_3455del NP_775907.4:p.Ala1152CysfsTer5
XM_005258809.2:c.3358_3359del XP_005258866.1:p.Ala1120CysfsTer5
XM_011526837.1:c.3454_3455del XP_011525139.1:p.Ala1152CysfsTer5
XM_011526838.1:c.3220_3221del XP_011525140.1:p.Ala1074CysfsTer5
XM_011526839.1:c.3118_3119del XP_011525141.1:p.Ala1040CysfsTer5
XM_011526840.1:c.2461_2462del XP_011525142.1:p.Ala821CysfsTer5
XM_011526841.1:c.2047_2048del XP_011525143.1:p.Ala683CysfsTer5
XM_011526842.1:c.1900_1901del XP_011525144.1:p.Ala634CysfsTer5
XM_011526843.1:c.1216_1217del XP_011525145.1:p.Ala406CysfsTer5
XM_011526844.1:c.1216_1217del XP_011525146.1:p.Ala406CysfsTer5
XM_011526840.2:c.2461_2462del XP_011525142.1:p.Ala821CysfsTer5
XM_011526841.2:c.2047_2048del XP_011525143.1:p.Ala683CysfsTer5
XM_011526844.2:c.1216_1217del XP_011525146.1:p.Ala406CysfsTer5
XM_017026665.1:c.3469_3470del XP_016882154.1:p.Ala1157CysfsTer5
NM_001083961.2:c.3469_3470del MANE Select NP_001077430.1:p.Ala1157CysfsTer5
NM_173636.5:c.3454_3455del NP_775907.4:p.Ala1152CysfsTer5