Canonical Allele Identifier: CA2333972223

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104627G= , CM000681.2:g.36104627G=	GRCh38
NC_000019.9:g.36595529G= , CM000681.1:g.36595529G=	GRCh37
NC_000019.8:g.41287369G=	NCBI36
NG_028101.1:g.54747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4248G=	ENSP00000270301.6:p.Leu1416=
ENST00000401500.7:c.4263G= MANE Select	ENSP00000384792.1:p.Leu1421=
ENST00000587391.6:c.*4123G=	ENSP00000465525.1:n.*4123G=
ENST00000679357.1:c.2343G=
ENST00000679598.1:c.1008G=
ENST00000679682.1:c.4248G=	ENSP00000506226.1:p.Leu1416=
ENST00000679714.1:c.4257G=	ENSP00000506627.1:p.Leu1419=
ENST00000679757.1:c.3912G=	ENSP00000505158.1:p.Leu1304=
ENST00000679858.1:c.*3645G=	ENSP00000505655.1:n.*3645G=
ENST00000680211.1:c.864G=	ENSP00000506102.1:p.Leu288=
ENST00000680280.1:n.1766G=
ENST00000680349.1:n.2912G=
ENST00000680403.1:c.4248G=	ENSP00000505677.1:p.Leu1416=
ENST00000680564.1:c.4014G=	ENSP00000505582.1:p.Leu1338=
ENST00000680590.1:c.*2643G=	ENSP00000505350.1:n.*2643G=
ENST00000680597.1:c.996G=
ENST00000680739.1:c.1278G=
ENST00000680773.1:n.2764G=
ENST00000680806.1:c.*3566G=	ENSP00000506418.1:n.*3566G=
ENST00000680997.1:n.2195G=
ENST00000681608.1:n.2108G=
ENST00000681625.1:c.*1595G=	ENSP00000505555.1:n.*1595G=
ENST00000681648.1:n.2314G=
ENST00000270301.11:c.4248G=	ENSP00000270301.6:p.Leu1416=
ENST00000401500.6:c.4263G=	ENSP00000384792.1:p.Leu1421=
ENST00000587391.5:c.*4123G=	ENSP00000465525.1:n.*4123G=
NM_001083961.1:c.4263G=	NP_001077430.1:p.Leu1421=
NM_173636.4:c.4248G=	NP_775907.4:p.Leu1416=
XM_005258809.2:c.4152G=	XP_005258866.1:p.Leu1384=
XM_011526837.1:c.4248G=	XP_011525139.1:p.Leu1416=
XM_011526838.1:c.4014G=	XP_011525140.1:p.Leu1338=
XM_011526839.1:c.3912G=	XP_011525141.1:p.Leu1304=
XM_011526840.1:c.3255G=	XP_011525142.1:p.Leu1085=
XM_011526841.1:c.2841G=	XP_011525143.1:p.Leu947=
XM_011526842.1:c.2694G=	XP_011525144.1:p.Leu898=
XM_011526843.1:c.2010G=	XP_011525145.1:p.Leu670=
XM_011526844.1:c.2010G=	XP_011525146.1:p.Leu670=
XM_011526840.2:c.3255G=	XP_011525142.1:p.Leu1085=
XM_011526841.2:c.2841G=	XP_011525143.1:p.Leu947=
XM_011526844.2:c.2010G=	XP_011525146.1:p.Leu670=
XM_017026665.1:c.4263G=	XP_016882154.1:p.Leu1421=
NM_001083961.2:c.4263G= MANE Select	NP_001077430.1:p.Leu1421=
NM_173636.5:c.4248G=	NP_775907.4:p.Leu1416=