Canonical Allele Identifier: CA2333970902

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102020C= , CM000681.2:g.36102020C=	GRCh38
NC_000019.9:g.36592922C= , CM000681.1:g.36592922C=	GRCh37
NC_000019.8:g.41284762C=	NCBI36
NG_028101.1:g.52140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3089C=	ENSP00000270301.6:p.Ala1030=
ENST00000401500.7:c.3089C= MANE Select	ENSP00000384792.1:p.Ala1030=
ENST00000587391.6:c.*2364C=	ENSP00000465525.1:n.*2364C=
ENST00000679357.1:c.879C=
ENST00000679422.1:c.768C=
ENST00000679682.1:c.3074C=	ENSP00000506226.1:p.Ala1025=
ENST00000679714.1:c.3083C=	ENSP00000506627.1:p.Ala1028=
ENST00000679757.1:c.2738C=	ENSP00000505158.1:p.Ala913=
ENST00000679858.1:c.*2471C=	ENSP00000505655.1:n.*2471C=
ENST00000680211.1:c.-311C=	ENSP00000506102.1:n.-311C=
ENST00000680349.1:n.1072C=
ENST00000680403.1:c.3089C=	ENSP00000505677.1:p.Ala1030=
ENST00000680564.1:c.2971+703C=	ENSP00000505582.1:n.2971+703C=
ENST00000680590.1:c.*1484C=	ENSP00000505350.1:n.*1484C=
ENST00000680739.1:c.7C=
ENST00000680773.1:n.1005C=
ENST00000680806.1:c.*1807C=	ENSP00000506418.1:n.*1807C=
ENST00000680997.1:n.436C=
ENST00000681088.1:c.751C=
ENST00000681608.1:n.37C=
ENST00000681625.1:c.*421C=	ENSP00000505555.1:n.*421C=
ENST00000270301.11:c.3089C=	ENSP00000270301.6:p.Ala1030=
ENST00000401500.6:c.3089C=	ENSP00000384792.1:p.Ala1030=
ENST00000587391.5:c.*2364C=	ENSP00000465525.1:n.*2364C=
NM_001083961.1:c.3089C=	NP_001077430.1:p.Ala1030=
NM_173636.4:c.3089C=	NP_775907.4:p.Ala1030=
XM_005258809.2:c.2978C=	XP_005258866.1:p.Ala993=
XM_011526837.1:c.3074C=	XP_011525139.1:p.Ala1025=
XM_011526838.1:c.2971+703C=	XP_011525140.1:n.2971+703C=
XM_011526839.1:c.2738C=	XP_011525141.1:p.Ala913=
XM_011526840.1:c.2081C=	XP_011525142.1:p.Ala694=
XM_011526841.1:c.1667C=	XP_011525143.1:p.Ala556=
XM_011526842.1:c.1520C=	XP_011525144.1:p.Ala507=
XM_011526843.1:c.836C=	XP_011525145.1:p.Ala279=
XM_011526844.1:c.836C=	XP_011525146.1:p.Ala279=
XM_011526840.2:c.2081C=	XP_011525142.1:p.Ala694=
XM_011526841.2:c.1667C=	XP_011525143.1:p.Ala556=
XM_011526844.2:c.836C=	XP_011525146.1:p.Ala279=
XM_017026665.1:c.3089C=	XP_016882154.1:p.Ala1030=
NM_001083961.2:c.3089C= MANE Select	NP_001077430.1:p.Ala1030=
NM_173636.5:c.3089C=	NP_775907.4:p.Ala1030=