Canonical Allele Identifier: CA2333970732

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101702G= , CM000681.2:g.36101702G=	GRCh38
NC_000019.9:g.36592604G= , CM000681.1:g.36592604G=	GRCh37
NC_000019.8:g.41284444G=	NCBI36
NG_028101.1:g.51822G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3010G=	ENSP00000270301.6:p.Ala1004=
ENST00000401500.7:c.3010G= MANE Select	ENSP00000384792.1:p.Ala1004=
ENST00000587391.6:c.*2046G=	ENSP00000465525.1:n.*2046G=
ENST00000679357.1:c.800G=
ENST00000679422.1:c.762-312G=
ENST00000679682.1:c.2995G=	ENSP00000506226.1:p.Ala999=
ENST00000679714.1:c.3004G=	ENSP00000506627.1:p.Ala1002=
ENST00000679757.1:c.2659G=	ENSP00000505158.1:p.Ala887=
ENST00000679858.1:c.*2153G=	ENSP00000505655.1:n.*2153G=
ENST00000680211.1:c.-390G=	ENSP00000506102.1:n.-390G=
ENST00000680349.1:n.993G=
ENST00000680403.1:c.3010G=	ENSP00000505677.1:p.Ala1004=
ENST00000680564.1:c.2971+385G=	ENSP00000505582.1:n.2971+385G=
ENST00000680590.1:c.*1405G=	ENSP00000505350.1:n.*1405G=
ENST00000680773.1:n.687G=
ENST00000680806.1:c.*1801-312G=	ENSP00000506418.1:n.*1801-312G=
ENST00000680997.1:n.357G=
ENST00000681088.1:c.672G=
ENST00000681625.1:c.*342G=	ENSP00000505555.1:n.*342G=
ENST00000270301.11:c.3010G=	ENSP00000270301.6:p.Ala1004=
ENST00000401500.6:c.3010G=	ENSP00000384792.1:p.Ala1004=
ENST00000587391.5:c.*2046G=	ENSP00000465525.1:n.*2046G=
NM_001083961.1:c.3010G=	NP_001077430.1:p.Ala1004=
NM_173636.4:c.3010G=	NP_775907.4:p.Ala1004=
XM_005258809.2:c.2972-312G=	XP_005258866.1:n.2972-312G=
XM_011526837.1:c.2995G=	XP_011525139.1:p.Ala999=
XM_011526838.1:c.2971+385G=	XP_011525140.1:n.2971+385G=
XM_011526839.1:c.2659G=	XP_011525141.1:p.Ala887=
XM_011526840.1:c.2002G=	XP_011525142.1:p.Ala668=
XM_011526841.1:c.1588G=	XP_011525143.1:p.Ala530=
XM_011526842.1:c.1441G=	XP_011525144.1:p.Ala481=
XM_011526843.1:c.757G=	XP_011525145.1:p.Ala253=
XM_011526844.1:c.757G=	XP_011525146.1:p.Ala253=
XM_011526840.2:c.2002G=	XP_011525142.1:p.Ala668=
XM_011526841.2:c.1588G=	XP_011525143.1:p.Ala530=
XM_011526844.2:c.757G=	XP_011525146.1:p.Ala253=
XM_017026665.1:c.3010G=	XP_016882154.1:p.Ala1004=
NM_001083961.2:c.3010G= MANE Select	NP_001077430.1:p.Ala1004=
NM_173636.5:c.3010G=	NP_775907.4:p.Ala1004=