Canonical Allele Identifier: CA405449004
Gene: WDR62 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36101679A>G , CM000681.2:g.36101679A>G GRCh38
NC_000019.9:g.36592581A>G , CM000681.1:g.36592581A>G GRCh37
NC_000019.8:g.41284421A>G NCBI36
NG_028101.1:g.51799A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.2987A>G ENSP00000270301.6:p.Glu996Gly
ENST00000401500.7:c.2987A>G MANE Select ENSP00000384792.1:p.Glu996Gly
ENST00000587391.6:c.*2023A>G ENSP00000465525.1:n.*2023A>G
ENST00000679357.1:c.777A>G
ENST00000679422.1:c.762-335A>G
ENST00000679682.1:c.2972A>G ENSP00000506226.1:p.Glu991Gly
ENST00000679714.1:c.2981A>G ENSP00000506627.1:p.Glu994Gly
ENST00000679757.1:c.2636A>G ENSP00000505158.1:p.Glu879Gly
ENST00000679858.1:c.*2130A>G ENSP00000505655.1:n.*2130A>G
ENST00000680211.1:c.-413A>G ENSP00000506102.1:n.-413A>G
ENST00000680349.1:n.970A>G
ENST00000680403.1:c.2987A>G ENSP00000505677.1:p.Glu996Gly
ENST00000680564.1:c.2971+362A>G ENSP00000505582.1:n.2971+362A>G
ENST00000680590.1:c.*1382A>G ENSP00000505350.1:n.*1382A>G
ENST00000680773.1:n.664A>G
ENST00000680806.1:c.*1801-335A>G ENSP00000506418.1:n.*1801-335A>G
ENST00000680997.1:n.334A>G
ENST00000681088.1:c.649A>G
ENST00000681625.1:c.*319A>G ENSP00000505555.1:n.*319A>G
ENST00000270301.11:c.2987A>G ENSP00000270301.6:p.Glu996Gly
ENST00000401500.6:c.2987A>G ENSP00000384792.1:p.Glu996Gly
ENST00000587391.5:c.*2023A>G ENSP00000465525.1:n.*2023A>G
NM_001083961.1:c.2987A>G NP_001077430.1:p.Glu996Gly
NM_173636.4:c.2987A>G NP_775907.4:p.Glu996Gly
XM_005258809.2:c.2972-335A>G XP_005258866.1:n.2972-335A>G
XM_011526837.1:c.2972A>G XP_011525139.1:p.Glu991Gly
XM_011526838.1:c.2971+362A>G XP_011525140.1:n.2971+362A>G
XM_011526839.1:c.2636A>G XP_011525141.1:p.Glu879Gly
XM_011526840.1:c.1979A>G XP_011525142.1:p.Glu660Gly
XM_011526841.1:c.1565A>G XP_011525143.1:p.Glu522Gly
XM_011526842.1:c.1418A>G XP_011525144.1:p.Glu473Gly
XM_011526843.1:c.734A>G XP_011525145.1:p.Glu245Gly
XM_011526844.1:c.734A>G XP_011525146.1:p.Glu245Gly
XM_011526840.2:c.1979A>G XP_011525142.1:p.Glu660Gly
XM_011526841.2:c.1565A>G XP_011525143.1:p.Glu522Gly
XM_011526844.2:c.734A>G XP_011525146.1:p.Glu245Gly
XM_017026665.1:c.2987A>G XP_016882154.1:p.Glu996Gly
NM_001083961.2:c.2987A>G MANE Select NP_001077430.1:p.Glu996Gly
NM_173636.5:c.2987A>G NP_775907.4:p.Glu996Gly