Canonical Allele Identifier: CA2333971384

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102966T= , CM000681.2:g.36102966T=	GRCh38
NC_000019.9:g.36593868T= , CM000681.1:g.36593868T=	GRCh37
NC_000019.8:g.41285708T=	NCBI36
NG_028101.1:g.53086T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3339T=	ENSP00000270301.6:p.Pro1113=
ENST00000401500.7:c.3354T= MANE Select	ENSP00000384792.1:p.Pro1118=
ENST00000587391.6:c.*3214T=	ENSP00000465525.1:n.*3214T=
ENST00000679357.1:c.1434T=
ENST00000679598.1:c.119T=
ENST00000679682.1:c.3339T=	ENSP00000506226.1:p.Pro1113=
ENST00000679714.1:c.3348T=	ENSP00000506627.1:p.Pro1116=
ENST00000679757.1:c.3003T=	ENSP00000505158.1:p.Pro1001=
ENST00000679858.1:c.*2736T=	ENSP00000505655.1:n.*2736T=
ENST00000680211.1:c.-46T=	ENSP00000506102.1:n.-46T=
ENST00000680280.1:n.641T=
ENST00000680349.1:n.1922T=
ENST00000680403.1:c.3339T=	ENSP00000505677.1:p.Pro1113=
ENST00000680564.1:c.3105T=	ENSP00000505582.1:p.Pro1035=
ENST00000680590.1:c.*1734T=	ENSP00000505350.1:n.*1734T=
ENST00000680597.1:c.119T=
ENST00000680739.1:c.369T=
ENST00000680773.1:n.1855T=
ENST00000680806.1:c.*2657T=	ENSP00000506418.1:n.*2657T=
ENST00000680997.1:n.1286T=
ENST00000681608.1:n.983T=
ENST00000681625.1:c.*686T=	ENSP00000505555.1:n.*686T=
ENST00000681648.1:n.653T=
ENST00000270301.11:c.3339T=	ENSP00000270301.6:p.Pro1113=
ENST00000401500.6:c.3354T=	ENSP00000384792.1:p.Pro1118=
ENST00000587391.5:c.*3214T=	ENSP00000465525.1:n.*3214T=
NM_001083961.1:c.3354T=	NP_001077430.1:p.Pro1118=
NM_173636.4:c.3339T=	NP_775907.4:p.Pro1113=
XM_005258809.2:c.3243T=	XP_005258866.1:p.Pro1081=
XM_011526837.1:c.3339T=	XP_011525139.1:p.Pro1113=
XM_011526838.1:c.3105T=	XP_011525140.1:p.Pro1035=
XM_011526839.1:c.3003T=	XP_011525141.1:p.Pro1001=
XM_011526840.1:c.2346T=	XP_011525142.1:p.Pro782=
XM_011526841.1:c.1932T=	XP_011525143.1:p.Pro644=
XM_011526842.1:c.1785T=	XP_011525144.1:p.Pro595=
XM_011526843.1:c.1101T=	XP_011525145.1:p.Pro367=
XM_011526844.1:c.1101T=	XP_011525146.1:p.Pro367=
XM_011526840.2:c.2346T=	XP_011525142.1:p.Pro782=
XM_011526841.2:c.1932T=	XP_011525143.1:p.Pro644=
XM_011526844.2:c.1101T=	XP_011525146.1:p.Pro367=
XM_017026665.1:c.3354T=	XP_016882154.1:p.Pro1118=
NM_001083961.2:c.3354T= MANE Select	NP_001077430.1:p.Pro1118=
NM_173636.5:c.3339T=	NP_775907.4:p.Pro1113=