Canonical Allele Identifier: CA2333972219
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104620A= , CM000681.2:g.36104620A= GRCh38
NC_000019.9:g.36595522A= , CM000681.1:g.36595522A= GRCh37
NC_000019.8:g.41287362A= NCBI36
NG_028101.1:g.54740A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4241A= ENSP00000270301.6:p.Asn1414=
ENST00000401500.7:c.4256A= MANE Select ENSP00000384792.1:p.Asn1419=
ENST00000587391.6:c.*4116A= ENSP00000465525.1:n.*4116A=
ENST00000679357.1:c.2336A=
ENST00000679598.1:c.1001A=
ENST00000679682.1:c.4241A= ENSP00000506226.1:p.Asn1414=
ENST00000679714.1:c.4250A= ENSP00000506627.1:p.Asn1417=
ENST00000679757.1:c.3905A= ENSP00000505158.1:p.Asn1302=
ENST00000679858.1:c.*3638A= ENSP00000505655.1:n.*3638A=
ENST00000680211.1:c.857A= ENSP00000506102.1:p.Asn286=
ENST00000680280.1:n.1759A=
ENST00000680349.1:n.2905A=
ENST00000680403.1:c.4241A= ENSP00000505677.1:p.Asn1414=
ENST00000680564.1:c.4007A= ENSP00000505582.1:p.Asn1336=
ENST00000680590.1:c.*2636A= ENSP00000505350.1:n.*2636A=
ENST00000680597.1:c.989A=
ENST00000680739.1:c.1271A=
ENST00000680773.1:n.2757A=
ENST00000680806.1:c.*3559A= ENSP00000506418.1:n.*3559A=
ENST00000680997.1:n.2188A=
ENST00000681608.1:n.2101A=
ENST00000681625.1:c.*1588A= ENSP00000505555.1:n.*1588A=
ENST00000681648.1:n.2307A=
ENST00000270301.11:c.4241A= ENSP00000270301.6:p.Asn1414=
ENST00000401500.6:c.4256A= ENSP00000384792.1:p.Asn1419=
ENST00000587391.5:c.*4116A= ENSP00000465525.1:n.*4116A=
NM_001083961.1:c.4256A= NP_001077430.1:p.Asn1419=
NM_173636.4:c.4241A= NP_775907.4:p.Asn1414=
XM_005258809.2:c.4145A= XP_005258866.1:p.Asn1382=
XM_011526837.1:c.4241A= XP_011525139.1:p.Asn1414=
XM_011526838.1:c.4007A= XP_011525140.1:p.Asn1336=
XM_011526839.1:c.3905A= XP_011525141.1:p.Asn1302=
XM_011526840.1:c.3248A= XP_011525142.1:p.Asn1083=
XM_011526841.1:c.2834A= XP_011525143.1:p.Asn945=
XM_011526842.1:c.2687A= XP_011525144.1:p.Asn896=
XM_011526843.1:c.2003A= XP_011525145.1:p.Asn668=
XM_011526844.1:c.2003A= XP_011525146.1:p.Asn668=
XM_011526840.2:c.3248A= XP_011525142.1:p.Asn1083=
XM_011526841.2:c.2834A= XP_011525143.1:p.Asn945=
XM_011526844.2:c.2003A= XP_011525146.1:p.Asn668=
XM_017026665.1:c.4256A= XP_016882154.1:p.Asn1419=
NM_001083961.2:c.4256A= MANE Select NP_001077430.1:p.Asn1419=
NM_173636.5:c.4241A= NP_775907.4:p.Asn1414=