Canonical Allele Identifier: CA405460452

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595457G>C (hg19) ; chr19:g.36104555G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104555G>C , CM000681.2:g.36104555G>C	GRCh38
NC_000019.9:g.36595457G>C , CM000681.1:g.36595457G>C	GRCh37
NC_000019.8:g.41287297G>C	NCBI36
NG_028101.1:g.54675G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4176G>C	ENSP00000270301.6:p.Trp1392Cys
ENST00000401500.7:c.4191G>C MANE Select	ENSP00000384792.1:p.Trp1397Cys
ENST00000587391.6:c.*4051G>C	ENSP00000465525.1:n.*4051G>C
ENST00000679357.1:c.2271G>C
ENST00000679598.1:c.936G>C
ENST00000679682.1:c.4176G>C	ENSP00000506226.1:p.Trp1392Cys
ENST00000679714.1:c.4185G>C	ENSP00000506627.1:p.Trp1395Cys
ENST00000679757.1:c.3840G>C	ENSP00000505158.1:p.Trp1280Cys
ENST00000679858.1:c.*3573G>C	ENSP00000505655.1:n.*3573G>C
ENST00000680211.1:c.792G>C	ENSP00000506102.1:p.Trp264Cys
ENST00000680280.1:n.1694G>C
ENST00000680349.1:n.2840G>C
ENST00000680403.1:c.4176G>C	ENSP00000505677.1:p.Trp1392Cys
ENST00000680564.1:c.3942G>C	ENSP00000505582.1:p.Trp1314Cys
ENST00000680590.1:c.*2571G>C	ENSP00000505350.1:n.*2571G>C
ENST00000680597.1:c.924G>C
ENST00000680739.1:c.1206G>C
ENST00000680773.1:n.2692G>C
ENST00000680806.1:c.*3494G>C	ENSP00000506418.1:n.*3494G>C
ENST00000680997.1:n.2123G>C
ENST00000681608.1:n.2036G>C
ENST00000681625.1:c.*1523G>C	ENSP00000505555.1:n.*1523G>C
ENST00000681648.1:n.2242G>C
ENST00000270301.11:c.4176G>C	ENSP00000270301.6:p.Trp1392Cys
ENST00000401500.6:c.4191G>C	ENSP00000384792.1:p.Trp1397Cys
ENST00000587391.5:c.*4051G>C	ENSP00000465525.1:n.*4051G>C
NM_001083961.1:c.4191G>C	NP_001077430.1:p.Trp1397Cys
NM_173636.4:c.4176G>C	NP_775907.4:p.Trp1392Cys
XM_005258809.2:c.4080G>C	XP_005258866.1:p.Trp1360Cys
XM_011526837.1:c.4176G>C	XP_011525139.1:p.Trp1392Cys
XM_011526838.1:c.3942G>C	XP_011525140.1:p.Trp1314Cys
XM_011526839.1:c.3840G>C	XP_011525141.1:p.Trp1280Cys
XM_011526840.1:c.3183G>C	XP_011525142.1:p.Trp1061Cys
XM_011526841.1:c.2769G>C	XP_011525143.1:p.Trp923Cys
XM_011526842.1:c.2622G>C	XP_011525144.1:p.Trp874Cys
XM_011526843.1:c.1938G>C	XP_011525145.1:p.Trp646Cys
XM_011526844.1:c.1938G>C	XP_011525146.1:p.Trp646Cys
XM_011526840.2:c.3183G>C	XP_011525142.1:p.Trp1061Cys
XM_011526841.2:c.2769G>C	XP_011525143.1:p.Trp923Cys
XM_011526844.2:c.1938G>C	XP_011525146.1:p.Trp646Cys
XM_017026665.1:c.4191G>C	XP_016882154.1:p.Trp1397Cys
NM_001083961.2:c.4191G>C MANE Select	NP_001077430.1:p.Trp1397Cys
NM_173636.5:c.4176G>C	NP_775907.4:p.Trp1392Cys