Canonical Allele Identifier: CA2333971297
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102795C= , CM000681.2:g.36102795C= GRCh38
NC_000019.9:g.36593697C= , CM000681.1:g.36593697C= GRCh37
NC_000019.8:g.41285537C= NCBI36
NG_028101.1:g.52915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3264C= ENSP00000270301.6:p.Phe1088=
ENST00000401500.7:c.3279C= MANE Select ENSP00000384792.1:p.Phe1093=
ENST00000587391.6:c.*3139C= ENSP00000465525.1:n.*3139C=
ENST00000679357.1:c.1359C=
ENST00000679598.1:c.44C=
ENST00000679682.1:c.3264C= ENSP00000506226.1:p.Phe1088=
ENST00000679714.1:c.3273C= ENSP00000506627.1:p.Phe1091=
ENST00000679757.1:c.2928C= ENSP00000505158.1:p.Phe976=
ENST00000679858.1:c.*2661C= ENSP00000505655.1:n.*2661C=
ENST00000680211.1:c.-121C= ENSP00000506102.1:n.-121C=
ENST00000680280.1:n.566C=
ENST00000680349.1:n.1847C=
ENST00000680403.1:c.3264C= ENSP00000505677.1:p.Phe1088=
ENST00000680564.1:c.3030C= ENSP00000505582.1:p.Phe1010=
ENST00000680590.1:c.*1659C= ENSP00000505350.1:n.*1659C=
ENST00000680597.1:c.44C=
ENST00000680739.1:c.294C=
ENST00000680773.1:n.1780C=
ENST00000680806.1:c.*2582C= ENSP00000506418.1:n.*2582C=
ENST00000680997.1:n.1211C=
ENST00000681608.1:n.812C=
ENST00000681625.1:c.*611C= ENSP00000505555.1:n.*611C=
ENST00000681648.1:n.578C=
ENST00000270301.11:c.3264C= ENSP00000270301.6:p.Phe1088=
ENST00000401500.6:c.3279C= ENSP00000384792.1:p.Phe1093=
ENST00000587391.5:c.*3139C= ENSP00000465525.1:n.*3139C=
NM_001083961.1:c.3279C= NP_001077430.1:p.Phe1093=
NM_173636.4:c.3264C= NP_775907.4:p.Phe1088=
XM_005258809.2:c.3168C= XP_005258866.1:p.Phe1056=
XM_011526837.1:c.3264C= XP_011525139.1:p.Phe1088=
XM_011526838.1:c.3030C= XP_011525140.1:p.Phe1010=
XM_011526839.1:c.2928C= XP_011525141.1:p.Phe976=
XM_011526840.1:c.2271C= XP_011525142.1:p.Phe757=
XM_011526841.1:c.1857C= XP_011525143.1:p.Phe619=
XM_011526842.1:c.1710C= XP_011525144.1:p.Phe570=
XM_011526843.1:c.1026C= XP_011525145.1:p.Phe342=
XM_011526844.1:c.1026C= XP_011525146.1:p.Phe342=
XM_011526840.2:c.2271C= XP_011525142.1:p.Phe757=
XM_011526841.2:c.1857C= XP_011525143.1:p.Phe619=
XM_011526844.2:c.1026C= XP_011525146.1:p.Phe342=
XM_017026665.1:c.3279C= XP_016882154.1:p.Phe1093=
NM_001083961.2:c.3279C= MANE Select NP_001077430.1:p.Phe1093=
NM_173636.5:c.3264C= NP_775907.4:p.Phe1088=