Canonical Allele Identifier: CA2333970936
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102092C= , CM000681.2:g.36102092C= GRCh38
NC_000019.9:g.36592994C= , CM000681.1:g.36592994C= GRCh37
NC_000019.8:g.41284834C= NCBI36
NG_028101.1:g.52212C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3161C= ENSP00000270301.6:p.Pro1054=
ENST00000401500.7:c.3161C= MANE Select ENSP00000384792.1:p.Pro1054=
ENST00000587391.6:c.*2436C= ENSP00000465525.1:n.*2436C=
ENST00000679357.1:c.951C=
ENST00000679422.1:c.840C=
ENST00000679682.1:c.3146C= ENSP00000506226.1:p.Pro1049=
ENST00000679714.1:c.3155C= ENSP00000506627.1:p.Pro1052=
ENST00000679757.1:c.2810C= ENSP00000505158.1:p.Pro937=
ENST00000679858.1:c.*2543C= ENSP00000505655.1:n.*2543C=
ENST00000680211.1:c.-239C= ENSP00000506102.1:n.-239C=
ENST00000680349.1:n.1144C=
ENST00000680403.1:c.3161C= ENSP00000505677.1:p.Pro1054=
ENST00000680564.1:c.2972-645C= ENSP00000505582.1:n.2972-645C=
ENST00000680590.1:c.*1556C= ENSP00000505350.1:n.*1556C=
ENST00000680739.1:c.79C=
ENST00000680773.1:n.1077C=
ENST00000680806.1:c.*1879C= ENSP00000506418.1:n.*1879C=
ENST00000680997.1:n.508C=
ENST00000681088.1:c.823C=
ENST00000681608.1:n.109C=
ENST00000681625.1:c.*493C= ENSP00000505555.1:n.*493C=
ENST00000270301.11:c.3161C= ENSP00000270301.6:p.Pro1054=
ENST00000401500.6:c.3161C= ENSP00000384792.1:p.Pro1054=
ENST00000587391.5:c.*2436C= ENSP00000465525.1:n.*2436C=
NM_001083961.1:c.3161C= NP_001077430.1:p.Pro1054=
NM_173636.4:c.3161C= NP_775907.4:p.Pro1054=
XM_005258809.2:c.3050C= XP_005258866.1:p.Pro1017=
XM_011526837.1:c.3146C= XP_011525139.1:p.Pro1049=
XM_011526838.1:c.2972-645C= XP_011525140.1:n.2972-645C=
XM_011526839.1:c.2810C= XP_011525141.1:p.Pro937=
XM_011526840.1:c.2153C= XP_011525142.1:p.Pro718=
XM_011526841.1:c.1739C= XP_011525143.1:p.Pro580=
XM_011526842.1:c.1592C= XP_011525144.1:p.Pro531=
XM_011526843.1:c.908C= XP_011525145.1:p.Pro303=
XM_011526844.1:c.908C= XP_011525146.1:p.Pro303=
XM_011526840.2:c.2153C= XP_011525142.1:p.Pro718=
XM_011526841.2:c.1739C= XP_011525143.1:p.Pro580=
XM_011526844.2:c.908C= XP_011525146.1:p.Pro303=
XM_017026665.1:c.3161C= XP_016882154.1:p.Pro1054=
NM_001083961.2:c.3161C= MANE Select NP_001077430.1:p.Pro1054=
NM_173636.5:c.3161C= NP_775907.4:p.Pro1054=