Canonical Allele Identifier: CA2333970970
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102155G= , CM000681.2:g.36102155G= GRCh38
NC_000019.9:g.36593057G= , CM000681.1:g.36593057G= GRCh37
NC_000019.8:g.41284897G= NCBI36
NG_028101.1:g.52275G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3220+4G= ENSP00000270301.6:n.3220+4G=
ENST00000401500.7:c.3220+4G= MANE Select ENSP00000384792.1:n.3220+4G=
ENST00000587391.6:c.*2499G= ENSP00000465525.1:n.*2499G=
ENST00000679357.1:c.1010+4G=
ENST00000679682.1:c.3205+4G= ENSP00000506226.1:n.3205+4G=
ENST00000679714.1:c.3214+4G= ENSP00000506627.1:n.3214+4G=
ENST00000679757.1:c.2869+4G= ENSP00000505158.1:n.2869+4G=
ENST00000679858.1:c.*2602+4G= ENSP00000505655.1:n.*2602+4G=
ENST00000680211.1:c.-180+4G= ENSP00000506102.1:n.-180+4G=
ENST00000680349.1:n.1207G=
ENST00000680403.1:c.3220+4G= ENSP00000505677.1:n.3220+4G=
ENST00000680564.1:c.2972-582G= ENSP00000505582.1:n.2972-582G=
ENST00000680590.1:c.*1615+4G= ENSP00000505350.1:n.*1615+4G=
ENST00000680739.1:c.142G=
ENST00000680773.1:n.1140G=
ENST00000680806.1:c.*1942G= ENSP00000506418.1:n.*1942G=
ENST00000680997.1:n.571G=
ENST00000681608.1:n.172G=
ENST00000681625.1:c.*552+4G= ENSP00000505555.1:n.*552+4G=
ENST00000270301.11:c.3220+4G= ENSP00000270301.6:n.3220+4G=
ENST00000401500.6:c.3220+4G= ENSP00000384792.1:n.3220+4G=
ENST00000587391.5:c.*2499G= ENSP00000465525.1:n.*2499G=
NM_001083961.1:c.3220+4G= NP_001077430.1:n.3220+4G=
NM_173636.4:c.3220+4G= NP_775907.4:n.3220+4G=
XM_005258809.2:c.3109+4G= XP_005258866.1:n.3109+4G=
XM_011526837.1:c.3205+4G= XP_011525139.1:n.3205+4G=
XM_011526838.1:c.2972-582G= XP_011525140.1:n.2972-582G=
XM_011526839.1:c.2869+4G= XP_011525141.1:n.2869+4G=
XM_011526840.1:c.2212+4G= XP_011525142.1:n.2212+4G=
XM_011526841.1:c.1798+4G= XP_011525143.1:n.1798+4G=
XM_011526842.1:c.1651+4G= XP_011525144.1:n.1651+4G=
XM_011526843.1:c.967+4G= XP_011525145.1:n.967+4G=
XM_011526844.1:c.967+4G= XP_011525146.1:n.967+4G=
XM_011526840.2:c.2212+4G= XP_011525142.1:n.2212+4G=
XM_011526841.2:c.1798+4G= XP_011525143.1:n.1798+4G=
XM_011526844.2:c.967+4G= XP_011525146.1:n.967+4G=
XM_017026665.1:c.3220+4G= XP_016882154.1:n.3220+4G=
NM_001083961.2:c.3220+4G= MANE Select NP_001077430.1:n.3220+4G=
NM_173636.5:c.3220+4G= NP_775907.4:n.3220+4G=