Canonical Allele Identifier: CA9396182
Gene: WDR62 HGNC NCBI

Linked Data

dbSNP Id: rs771720762

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102148_36102178del , CM000681.2:g.36102148_36102178del GRCh38
NC_000019.9:g.36593050_36593080del , CM000681.1:g.36593050_36593080del GRCh37
NC_000019.8:g.41284890_41284920del NCBI36
NG_028101.1:g.52268_52298del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3217_3220+27del
ENST00000401500.7:c.3217_3220+27del
ENST00000587391.6:c.*2492_*2522del ENSP00000465525.1:n.*2492_*2522del
ENST00000679357.1:c.1007_1010+27del
ENST00000679682.1:c.3202_3205+27del
ENST00000679714.1:c.3211_3214+27del
ENST00000679757.1:c.2866_2869+27del
ENST00000679858.1:c.*2599_*2602+27del
ENST00000680211.1:c.-183_-180+27del
ENST00000680349.1:n.1200_1230del
ENST00000680403.1:c.3217_3220+27del
ENST00000680564.1:c.2972-589_2972-559del ENSP00000505582.1:n.2972-589_2972-559del
ENST00000680590.1:c.*1612_*1615+27del
ENST00000680739.1:c.135_165del
ENST00000680773.1:n.1133_1163del
ENST00000680806.1:c.*1935_*1965del ENSP00000506418.1:n.*1935_*1965del
ENST00000680997.1:n.564_594del
ENST00000681608.1:n.165_195del
ENST00000681625.1:c.*549_*552+27del
ENST00000270301.11:c.3217_3220+27del
ENST00000401500.6:c.3217_3220+27del
ENST00000587391.5:c.*2492_*2522del ENSP00000465525.1:n.*2492_*2522del
NM_001083961.1:c.3217_3220+27del
NM_173636.4:c.3217_3220+27del
XM_005258809.2:c.3106_3109+27del
XM_011526837.1:c.3202_3205+27del
XM_011526838.1:c.2972-589_2972-559del XP_011525140.1:n.2972-589_2972-559del
XM_011526839.1:c.2866_2869+27del
XM_011526840.1:c.2209_2212+27del
XM_011526841.1:c.1795_1798+27del
XM_011526842.1:c.1648_1651+27del
XM_011526843.1:c.964_967+27del
XM_011526844.1:c.964_967+27del
XM_011526840.2:c.2209_2212+27del
XM_011526841.2:c.1795_1798+27del
XM_011526844.2:c.964_967+27del
XM_017026665.1:c.3217_3220+27del
NM_001083961.2:c.3217_3220+27del
NM_173636.5:c.3217_3220+27del