Canonical Allele Identifier: CA2333971381

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102961T= , CM000681.2:g.36102961T=	GRCh38
NC_000019.9:g.36593863T= , CM000681.1:g.36593863T=	GRCh37
NC_000019.8:g.41285703T=	NCBI36
NG_028101.1:g.53081T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3334T=	ENSP00000270301.6:p.Phe1112=
ENST00000401500.7:c.3349T= MANE Select	ENSP00000384792.1:p.Phe1117=
ENST00000587391.6:c.*3209T=	ENSP00000465525.1:n.*3209T=
ENST00000679357.1:c.1429T=
ENST00000679598.1:c.114T=
ENST00000679682.1:c.3334T=	ENSP00000506226.1:p.Phe1112=
ENST00000679714.1:c.3343T=	ENSP00000506627.1:p.Phe1115=
ENST00000679757.1:c.2998T=	ENSP00000505158.1:p.Phe1000=
ENST00000679858.1:c.*2731T=	ENSP00000505655.1:n.*2731T=
ENST00000680211.1:c.-51T=	ENSP00000506102.1:n.-51T=
ENST00000680280.1:n.636T=
ENST00000680349.1:n.1917T=
ENST00000680403.1:c.3334T=	ENSP00000505677.1:p.Phe1112=
ENST00000680564.1:c.3100T=	ENSP00000505582.1:p.Phe1034=
ENST00000680590.1:c.*1729T=	ENSP00000505350.1:n.*1729T=
ENST00000680597.1:c.114T=
ENST00000680739.1:c.364T=
ENST00000680773.1:n.1850T=
ENST00000680806.1:c.*2652T=	ENSP00000506418.1:n.*2652T=
ENST00000680997.1:n.1281T=
ENST00000681608.1:n.978T=
ENST00000681625.1:c.*681T=	ENSP00000505555.1:n.*681T=
ENST00000681648.1:n.648T=
ENST00000270301.11:c.3334T=	ENSP00000270301.6:p.Phe1112=
ENST00000401500.6:c.3349T=	ENSP00000384792.1:p.Phe1117=
ENST00000587391.5:c.*3209T=	ENSP00000465525.1:n.*3209T=
NM_001083961.1:c.3349T=	NP_001077430.1:p.Phe1117=
NM_173636.4:c.3334T=	NP_775907.4:p.Phe1112=
XM_005258809.2:c.3238T=	XP_005258866.1:p.Phe1080=
XM_011526837.1:c.3334T=	XP_011525139.1:p.Phe1112=
XM_011526838.1:c.3100T=	XP_011525140.1:p.Phe1034=
XM_011526839.1:c.2998T=	XP_011525141.1:p.Phe1000=
XM_011526840.1:c.2341T=	XP_011525142.1:p.Phe781=
XM_011526841.1:c.1927T=	XP_011525143.1:p.Phe643=
XM_011526842.1:c.1780T=	XP_011525144.1:p.Phe594=
XM_011526843.1:c.1096T=	XP_011525145.1:p.Phe366=
XM_011526844.1:c.1096T=	XP_011525146.1:p.Phe366=
XM_011526840.2:c.2341T=	XP_011525142.1:p.Phe781=
XM_011526841.2:c.1927T=	XP_011525143.1:p.Phe643=
XM_011526844.2:c.1096T=	XP_011525146.1:p.Phe366=
XM_017026665.1:c.3349T=	XP_016882154.1:p.Phe1117=
NM_001083961.2:c.3349T= MANE Select	NP_001077430.1:p.Phe1117=
NM_173636.5:c.3334T=	NP_775907.4:p.Phe1112=