Canonical Allele Identifier: CA2814265370
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102854_36102949del , CM000681.2:g.36102854_36102949del GRCh38
NC_000019.9:g.36593756_36593851del , CM000681.1:g.36593756_36593851del GRCh37
NC_000019.8:g.41285596_41285691del NCBI36
NG_028101.1:g.52974_53069del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3320+3_3322del
ENST00000401500.7:c.3335+3_3337del
ENST00000587391.6:c.*3195+3_*3197del
ENST00000679357.1:c.1415+3_1417del
ENST00000679598.1:c.100+3_102del
ENST00000679682.1:c.3320+3_3322del
ENST00000679714.1:c.3329+3_3331del
ENST00000679757.1:c.2984+3_2986del
ENST00000679858.1:c.*2717+3_*2719del
ENST00000680211.1:c.-65+3_-63del
ENST00000680280.1:n.622+3_624del
ENST00000680349.1:n.1903+3_1905del
ENST00000680403.1:c.3320+3_3322del
ENST00000680564.1:c.3086+3_3088del
ENST00000680590.1:c.*1715+3_*1717del
ENST00000680597.1:c.100+3_102del
ENST00000680739.1:c.350+3_352del
ENST00000680773.1:n.1836+3_1838del
ENST00000680806.1:c.*2638+3_*2640del
ENST00000680997.1:n.1267+3_1269del
ENST00000681608.1:n.871_966del
ENST00000681625.1:c.*667+3_*669del
ENST00000681648.1:n.634+3_636del
ENST00000270301.11:c.3320+3_3322del
ENST00000401500.6:c.3335+3_3337del
ENST00000587391.5:c.*3195+3_*3197del
NM_001083961.1:c.3335+3_3337del
NM_173636.4:c.3320+3_3322del
XM_005258809.2:c.3224+3_3226del
XM_011526837.1:c.3320+3_3322del
XM_011526838.1:c.3086+3_3088del
XM_011526839.1:c.2984+3_2986del
XM_011526840.1:c.2327+3_2329del
XM_011526841.1:c.1913+3_1915del
XM_011526842.1:c.1766+3_1768del
XM_011526843.1:c.1082+3_1084del
XM_011526844.1:c.1082+3_1084del
XM_011526840.2:c.2327+3_2329del
XM_011526841.2:c.1913+3_1915del
XM_011526844.2:c.1082+3_1084del
XM_017026665.1:c.3335+3_3337del
NM_001083961.2:c.3335+3_3337del
NM_173636.5:c.3320+3_3322del