Canonical Allele Identifier: CA2333971308
Community Standard Title: NM_001083961.2(WDR62):c.3304C= (p.Gln1102=)
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102820C= , CM000681.2:g.36102820C= GRCh38
NC_000019.9:g.36593722C= , CM000681.1:g.36593722C= GRCh37
NC_000019.8:g.41285562C= NCBI36
NG_028101.1:g.52940C=

Transcript Alleles

HGVS Amino-acid Change
NM_001083961.2:c.3304C= MANE Select NP_001077430.1:p.Gln1102=
ENST00000401500.7:c.3304C= MANE Select ENSP00000384792.1:p.Gln1102=
NM_001083961.1:c.3304C= NP_001077430.1:p.Gln1102=
NM_173636.4:c.3289C= NP_775907.4:p.Gln1097=
NM_173636.5:c.3289C= NP_775907.4:p.Gln1097=
ENST00000270301.11:c.3289C= ENSP00000270301.6:p.Gln1097=
ENST00000270301.12:c.3289C= ENSP00000270301.6:p.Gln1097=
ENST00000401500.6:c.3304C= ENSP00000384792.1:p.Gln1102=
ENST00000587391.5:c.*3164C= ENSP00000465525.1:n.*3164C=
ENST00000587391.6:c.*3164C= ENSP00000465525.1:n.*3164C=
ENST00000679357.1:c.1384C=
ENST00000679598.1:c.69C=
ENST00000679682.1:c.3289C= ENSP00000506226.1:p.Gln1097=
ENST00000679714.1:c.3298C= ENSP00000506627.1:p.Gln1100=
ENST00000679757.1:c.2953C= ENSP00000505158.1:p.Gln985=
ENST00000679858.1:c.*2686C= ENSP00000505655.1:n.*2686C=
ENST00000680211.1:c.-96C= ENSP00000506102.1:n.-96C=
ENST00000680280.1:n.591C=
ENST00000680349.1:n.1872C=
ENST00000680403.1:c.3289C= ENSP00000505677.1:p.Gln1097=
ENST00000680564.1:c.3055C= ENSP00000505582.1:p.Gln1019=
ENST00000680590.1:c.*1684C= ENSP00000505350.1:n.*1684C=
ENST00000680597.1:c.69C=
ENST00000680739.1:c.319C=
ENST00000680773.1:n.1805C=
ENST00000680806.1:c.*2607C= ENSP00000506418.1:n.*2607C=
ENST00000680997.1:n.1236C=
ENST00000681608.1:n.837C=
ENST00000681625.1:c.*636C= ENSP00000505555.1:n.*636C=
ENST00000681648.1:n.603C=
XM_005258809.2:c.3193C= XP_005258866.1:p.Gln1065=
XM_011526837.1:c.3289C= XP_011525139.1:p.Gln1097=
XM_011526838.1:c.3055C= XP_011525140.1:p.Gln1019=
XM_011526839.1:c.2953C= XP_011525141.1:p.Gln985=
XM_011526840.1:c.2296C= XP_011525142.1:p.Gln766=
XM_011526840.2:c.2296C= XP_011525142.1:p.Gln766=
XM_011526841.1:c.1882C= XP_011525143.1:p.Gln628=
XM_011526841.2:c.1882C= XP_011525143.1:p.Gln628=
XM_011526842.1:c.1735C= XP_011525144.1:p.Gln579=
XM_011526843.1:c.1051C= XP_011525145.1:p.Gln351=
XM_011526844.1:c.1051C= XP_011525146.1:p.Gln351=
XM_011526844.2:c.1051C= XP_011525146.1:p.Gln351=
XM_017026665.1:c.3304C= XP_016882154.1:p.Gln1102=