Canonical Allele Identifier: CA2333961203

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36081512G= , CM000681.2:g.36081512G=	GRCh38
NC_000019.9:g.36572414G= , CM000681.1:g.36572414G=	GRCh37
NC_000019.8:g.41264254G=	NCBI36
NG_028101.1:g.31632G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001083961.2:c.1313G= MANE Select	NP_001077430.1:p.Arg438=
ENST00000401500.7:c.1313G= MANE Select	ENSP00000384792.1:p.Arg438=
NM_001083961.1:c.1313G=	NP_001077430.1:p.Arg438=
NM_173636.4:c.1313G=	NP_775907.4:p.Arg438=
NM_173636.5:c.1313G=	NP_775907.4:p.Arg438=
ENST00000270301.11:c.1313G=	ENSP00000270301.6:p.Arg438=
ENST00000270301.12:c.1313G=	ENSP00000270301.6:p.Arg438=
ENST00000401500.6:c.1313G=	ENSP00000384792.1:p.Arg438=
ENST00000587391.5:c.1313G=	ENSP00000465525.1:p.Arg438=
ENST00000587391.6:c.1313G=	ENSP00000465525.1:p.Arg438=
ENST00000644764.2:c.*105G=	ENSP00000494253.2:n.*105G=
ENST00000679682.1:c.1298G=	ENSP00000506226.1:p.Arg433=
ENST00000679714.1:c.1307G=	ENSP00000506627.1:p.Arg436=
ENST00000679757.1:c.962G=	ENSP00000505158.1:p.Arg321=
ENST00000679858.1:c.*110G=	ENSP00000505655.1:n.*110G=
ENST00000680359.1:c.1313G=	ENSP00000506079.1:p.Arg438=
ENST00000680403.1:c.1313G=	ENSP00000505677.1:p.Arg438=
ENST00000680489.1:n.1636G=
ENST00000680564.1:c.1313G=	ENSP00000505582.1:p.Arg438=
ENST00000680590.1:c.1313G=	ENSP00000505350.1:p.Arg438=
ENST00000680806.1:c.*142G=	ENSP00000506418.1:n.*142G=
ENST00000681625.1:c.1298G=	ENSP00000505555.1:p.Arg433=
XM_005258809.2:c.1313G=	XP_005258866.1:p.Arg438=
XM_011526837.1:c.1298G=	XP_011525139.1:p.Arg433=
XM_011526838.1:c.1313G=	XP_011525140.1:p.Arg438=
XM_011526839.1:c.962G=	XP_011525141.1:p.Arg321=
XM_011526840.1:c.305G=	XP_011525142.1:p.Arg102=
XM_011526840.2:c.305G=	XP_011525142.1:p.Arg102=
XM_017026665.1:c.1313G=	XP_016882154.1:p.Arg438=
XR_001753671.1:n.1404G=
XR_001753672.1:n.1404G=