Canonical Allele Identifier: CA2333969716

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36099533C= , CM000681.2:g.36099533C=	GRCh38
NC_000019.9:g.36590435C= , CM000681.1:g.36590435C=	GRCh37
NC_000019.8:g.41282275C=	NCBI36
NG_028101.1:g.49653C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001083961.2:c.2655C= MANE Select	NP_001077430.1:p.Tyr885=
ENST00000401500.7:c.2655C= MANE Select	ENSP00000384792.1:p.Tyr885=
NM_001083961.1:c.2655C=	NP_001077430.1:p.Tyr885=
NM_173636.4:c.2655C=	NP_775907.4:p.Tyr885=
NM_173636.5:c.2655C=	NP_775907.4:p.Tyr885=
ENST00000270301.11:c.2655C=	ENSP00000270301.6:p.Tyr885=
ENST00000270301.12:c.2655C=	ENSP00000270301.6:p.Tyr885=
ENST00000401500.6:c.2655C=	ENSP00000384792.1:p.Tyr885=
ENST00000587391.5:c.*1345C=	ENSP00000465525.1:n.*1345C=
ENST00000587391.6:c.*1345C=	ENSP00000465525.1:n.*1345C=
ENST00000679357.1:c.445C=
ENST00000679422.1:c.445C=
ENST00000679682.1:c.2640C=	ENSP00000506226.1:p.Tyr880=
ENST00000679714.1:c.2649C=	ENSP00000506627.1:p.Tyr883=
ENST00000679757.1:c.2304C=	ENSP00000505158.1:p.Tyr768=
ENST00000679858.1:c.*1452C=	ENSP00000505655.1:n.*1452C=
ENST00000680349.1:n.638C=
ENST00000680377.1:c.929C=
ENST00000680403.1:c.2655C=	ENSP00000505677.1:p.Tyr885=
ENST00000680564.1:c.2655C=	ENSP00000505582.1:p.Tyr885=
ENST00000680590.1:c.*1054C=	ENSP00000505350.1:n.*1054C=
ENST00000680806.1:c.*1484C=	ENSP00000506418.1:n.*1484C=
ENST00000680858.1:c.853C=
ENST00000681088.1:c.445C=
ENST00000681302.1:c.1041C=
ENST00000681625.1:c.2636C=	ENSP00000505555.1:p.Thr879=
XM_005258809.2:c.2655C=	XP_005258866.1:p.Tyr885=
XM_011526837.1:c.2640C=	XP_011525139.1:p.Tyr880=
XM_011526838.1:c.2655C=	XP_011525140.1:p.Tyr885=
XM_011526839.1:c.2304C=	XP_011525141.1:p.Tyr768=
XM_011526840.1:c.1647C=	XP_011525142.1:p.Tyr549=
XM_011526840.2:c.1647C=	XP_011525142.1:p.Tyr549=
XM_011526841.1:c.1233C=	XP_011525143.1:p.Tyr411=
XM_011526841.2:c.1233C=	XP_011525143.1:p.Tyr411=
XM_011526842.1:c.1086C=	XP_011525144.1:p.Tyr362=
XM_011526843.1:c.402C=	XP_011525145.1:p.Tyr134=
XM_011526844.1:c.402C=	XP_011525146.1:p.Tyr134=
XM_011526844.2:c.402C=	XP_011525146.1:p.Tyr134=
XM_017026665.1:c.2655C=	XP_016882154.1:p.Tyr885=