Canonical Allele Identifier: CA2333972225

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104628C= , CM000681.2:g.36104628C=	GRCh38
NC_000019.9:g.36595530C= , CM000681.1:g.36595530C=	GRCh37
NC_000019.8:g.41287370C=	NCBI36
NG_028101.1:g.54748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4249C=	ENSP00000270301.6:p.His1417=
ENST00000401500.7:c.4264C= MANE Select	ENSP00000384792.1:p.His1422=
ENST00000587391.6:c.*4124C=	ENSP00000465525.1:n.*4124C=
ENST00000679357.1:c.2344C=
ENST00000679598.1:c.1009C=
ENST00000679682.1:c.4249C=	ENSP00000506226.1:p.His1417=
ENST00000679714.1:c.4258C=	ENSP00000506627.1:p.His1420=
ENST00000679757.1:c.3913C=	ENSP00000505158.1:p.His1305=
ENST00000679858.1:c.*3646C=	ENSP00000505655.1:n.*3646C=
ENST00000680211.1:c.865C=	ENSP00000506102.1:p.His289=
ENST00000680280.1:n.1767C=
ENST00000680349.1:n.2913C=
ENST00000680403.1:c.4249C=	ENSP00000505677.1:p.His1417=
ENST00000680564.1:c.4015C=	ENSP00000505582.1:p.His1339=
ENST00000680590.1:c.*2644C=	ENSP00000505350.1:n.*2644C=
ENST00000680597.1:c.997C=
ENST00000680739.1:c.1279C=
ENST00000680773.1:n.2765C=
ENST00000680806.1:c.*3567C=	ENSP00000506418.1:n.*3567C=
ENST00000680997.1:n.2196C=
ENST00000681608.1:n.2109C=
ENST00000681625.1:c.*1596C=	ENSP00000505555.1:n.*1596C=
ENST00000681648.1:n.2315C=
ENST00000270301.11:c.4249C=	ENSP00000270301.6:p.His1417=
ENST00000401500.6:c.4264C=	ENSP00000384792.1:p.His1422=
ENST00000587391.5:c.*4124C=	ENSP00000465525.1:n.*4124C=
NM_001083961.1:c.4264C=	NP_001077430.1:p.His1422=
NM_173636.4:c.4249C=	NP_775907.4:p.His1417=
XM_005258809.2:c.4153C=	XP_005258866.1:p.His1385=
XM_011526837.1:c.4249C=	XP_011525139.1:p.His1417=
XM_011526838.1:c.4015C=	XP_011525140.1:p.His1339=
XM_011526839.1:c.3913C=	XP_011525141.1:p.His1305=
XM_011526840.1:c.3256C=	XP_011525142.1:p.His1086=
XM_011526841.1:c.2842C=	XP_011525143.1:p.His948=
XM_011526842.1:c.2695C=	XP_011525144.1:p.His899=
XM_011526843.1:c.2011C=	XP_011525145.1:p.His671=
XM_011526844.1:c.2011C=	XP_011525146.1:p.His671=
XM_011526840.2:c.3256C=	XP_011525142.1:p.His1086=
XM_011526841.2:c.2842C=	XP_011525143.1:p.His948=
XM_011526844.2:c.2011C=	XP_011525146.1:p.His671=
XM_017026665.1:c.4264C=	XP_016882154.1:p.His1422=
NM_001083961.2:c.4264C= MANE Select	NP_001077430.1:p.His1422=
NM_173636.5:c.4249C=	NP_775907.4:p.His1417=