Canonical Allele Identifier: CA2333972192
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104562C= , CM000681.2:g.36104562C= GRCh38
NC_000019.9:g.36595464C= , CM000681.1:g.36595464C= GRCh37
NC_000019.8:g.41287304C= NCBI36
NG_028101.1:g.54682C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4183C= ENSP00000270301.6:p.Pro1395=
ENST00000401500.7:c.4198C= MANE Select ENSP00000384792.1:p.Pro1400=
ENST00000587391.6:c.*4058C= ENSP00000465525.1:n.*4058C=
ENST00000679357.1:c.2278C=
ENST00000679598.1:c.943C=
ENST00000679682.1:c.4183C= ENSP00000506226.1:p.Pro1395=
ENST00000679714.1:c.4192C= ENSP00000506627.1:p.Pro1398=
ENST00000679757.1:c.3847C= ENSP00000505158.1:p.Pro1283=
ENST00000679858.1:c.*3580C= ENSP00000505655.1:n.*3580C=
ENST00000680211.1:c.799C= ENSP00000506102.1:p.Pro267=
ENST00000680280.1:n.1701C=
ENST00000680349.1:n.2847C=
ENST00000680403.1:c.4183C= ENSP00000505677.1:p.Pro1395=
ENST00000680564.1:c.3949C= ENSP00000505582.1:p.Pro1317=
ENST00000680590.1:c.*2578C= ENSP00000505350.1:n.*2578C=
ENST00000680597.1:c.931C=
ENST00000680739.1:c.1213C=
ENST00000680773.1:n.2699C=
ENST00000680806.1:c.*3501C= ENSP00000506418.1:n.*3501C=
ENST00000680997.1:n.2130C=
ENST00000681608.1:n.2043C=
ENST00000681625.1:c.*1530C= ENSP00000505555.1:n.*1530C=
ENST00000681648.1:n.2249C=
ENST00000270301.11:c.4183C= ENSP00000270301.6:p.Pro1395=
ENST00000401500.6:c.4198C= ENSP00000384792.1:p.Pro1400=
ENST00000587391.5:c.*4058C= ENSP00000465525.1:n.*4058C=
NM_001083961.1:c.4198C= NP_001077430.1:p.Pro1400=
NM_173636.4:c.4183C= NP_775907.4:p.Pro1395=
XM_005258809.2:c.4087C= XP_005258866.1:p.Pro1363=
XM_011526837.1:c.4183C= XP_011525139.1:p.Pro1395=
XM_011526838.1:c.3949C= XP_011525140.1:p.Pro1317=
XM_011526839.1:c.3847C= XP_011525141.1:p.Pro1283=
XM_011526840.1:c.3190C= XP_011525142.1:p.Pro1064=
XM_011526841.1:c.2776C= XP_011525143.1:p.Pro926=
XM_011526842.1:c.2629C= XP_011525144.1:p.Pro877=
XM_011526843.1:c.1945C= XP_011525145.1:p.Pro649=
XM_011526844.1:c.1945C= XP_011525146.1:p.Pro649=
XM_011526840.2:c.3190C= XP_011525142.1:p.Pro1064=
XM_011526841.2:c.2776C= XP_011525143.1:p.Pro926=
XM_011526844.2:c.1945C= XP_011525146.1:p.Pro649=
XM_017026665.1:c.4198C= XP_016882154.1:p.Pro1400=
NM_001083961.2:c.4198C= MANE Select NP_001077430.1:p.Pro1400=
NM_173636.5:c.4183C= NP_775907.4:p.Pro1395=