Canonical Allele Identifier: CA2333970962

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102143C= , CM000681.2:g.36102143C=	GRCh38
NC_000019.9:g.36593045C= , CM000681.1:g.36593045C=	GRCh37
NC_000019.8:g.41284885C=	NCBI36
NG_028101.1:g.52263C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3212C=	ENSP00000270301.6:p.Pro1071=
ENST00000401500.7:c.3212C= MANE Select	ENSP00000384792.1:p.Pro1071=
ENST00000587391.6:c.*2487C=	ENSP00000465525.1:n.*2487C=
ENST00000679357.1:c.1002C=
ENST00000679422.1:c.891C=
ENST00000679682.1:c.3197C=	ENSP00000506226.1:p.Pro1066=
ENST00000679714.1:c.3206C=	ENSP00000506627.1:p.Pro1069=
ENST00000679757.1:c.2861C=	ENSP00000505158.1:p.Pro954=
ENST00000679858.1:c.*2594C=	ENSP00000505655.1:n.*2594C=
ENST00000680211.1:c.-188C=	ENSP00000506102.1:n.-188C=
ENST00000680349.1:n.1195C=
ENST00000680403.1:c.3212C=	ENSP00000505677.1:p.Pro1071=
ENST00000680564.1:c.2972-594C=	ENSP00000505582.1:n.2972-594C=
ENST00000680590.1:c.*1607C=	ENSP00000505350.1:n.*1607C=
ENST00000680739.1:c.130C=
ENST00000680773.1:n.1128C=
ENST00000680806.1:c.*1930C=	ENSP00000506418.1:n.*1930C=
ENST00000680997.1:n.559C=
ENST00000681088.1:c.874C=
ENST00000681608.1:n.160C=
ENST00000681625.1:c.*544C=	ENSP00000505555.1:n.*544C=
ENST00000270301.11:c.3212C=	ENSP00000270301.6:p.Pro1071=
ENST00000401500.6:c.3212C=	ENSP00000384792.1:p.Pro1071=
ENST00000587391.5:c.*2487C=	ENSP00000465525.1:n.*2487C=
NM_001083961.1:c.3212C=	NP_001077430.1:p.Pro1071=
NM_173636.4:c.3212C=	NP_775907.4:p.Pro1071=
XM_005258809.2:c.3101C=	XP_005258866.1:p.Pro1034=
XM_011526837.1:c.3197C=	XP_011525139.1:p.Pro1066=
XM_011526838.1:c.2972-594C=	XP_011525140.1:n.2972-594C=
XM_011526839.1:c.2861C=	XP_011525141.1:p.Pro954=
XM_011526840.1:c.2204C=	XP_011525142.1:p.Pro735=
XM_011526841.1:c.1790C=	XP_011525143.1:p.Pro597=
XM_011526842.1:c.1643C=	XP_011525144.1:p.Pro548=
XM_011526843.1:c.959C=	XP_011525145.1:p.Pro320=
XM_011526844.1:c.959C=	XP_011525146.1:p.Pro320=
XM_011526840.2:c.2204C=	XP_011525142.1:p.Pro735=
XM_011526841.2:c.1790C=	XP_011525143.1:p.Pro597=
XM_011526844.2:c.959C=	XP_011525146.1:p.Pro320=
XM_017026665.1:c.3212C=	XP_016882154.1:p.Pro1071=
NM_001083961.2:c.3212C= MANE Select	NP_001077430.1:p.Pro1071=
NM_173636.5:c.3212C=	NP_775907.4:p.Pro1071=