Canonical Allele Identifier: CA405460429

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595453G>T (hg19) ; chr19:g.36104551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104551G>T , CM000681.2:g.36104551G>T	GRCh38
NC_000019.9:g.36595453G>T , CM000681.1:g.36595453G>T	GRCh37
NC_000019.8:g.41287293G>T	NCBI36
NG_028101.1:g.54671G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4172G>T	ENSP00000270301.6:p.Arg1391Leu
ENST00000401500.7:c.4187G>T MANE Select	ENSP00000384792.1:p.Arg1396Leu
ENST00000587391.6:c.*4047G>T	ENSP00000465525.1:n.*4047G>T
ENST00000679357.1:c.2267G>T
ENST00000679598.1:c.932G>T
ENST00000679682.1:c.4172G>T	ENSP00000506226.1:p.Arg1391Leu
ENST00000679714.1:c.4181G>T	ENSP00000506627.1:p.Arg1394Leu
ENST00000679757.1:c.3836G>T	ENSP00000505158.1:p.Arg1279Leu
ENST00000679858.1:c.*3569G>T	ENSP00000505655.1:n.*3569G>T
ENST00000680211.1:c.788G>T	ENSP00000506102.1:p.Arg263Leu
ENST00000680280.1:n.1690G>T
ENST00000680349.1:n.2836G>T
ENST00000680403.1:c.4172G>T	ENSP00000505677.1:p.Arg1391Leu
ENST00000680564.1:c.3938G>T	ENSP00000505582.1:p.Arg1313Leu
ENST00000680590.1:c.*2567G>T	ENSP00000505350.1:n.*2567G>T
ENST00000680597.1:c.920G>T
ENST00000680739.1:c.1202G>T
ENST00000680773.1:n.2688G>T
ENST00000680806.1:c.*3490G>T	ENSP00000506418.1:n.*3490G>T
ENST00000680997.1:n.2119G>T
ENST00000681608.1:n.2032G>T
ENST00000681625.1:c.*1519G>T	ENSP00000505555.1:n.*1519G>T
ENST00000681648.1:n.2238G>T
ENST00000270301.11:c.4172G>T	ENSP00000270301.6:p.Arg1391Leu
ENST00000401500.6:c.4187G>T	ENSP00000384792.1:p.Arg1396Leu
ENST00000587391.5:c.*4047G>T	ENSP00000465525.1:n.*4047G>T
NM_001083961.1:c.4187G>T	NP_001077430.1:p.Arg1396Leu
NM_173636.4:c.4172G>T	NP_775907.4:p.Arg1391Leu
XM_005258809.2:c.4076G>T	XP_005258866.1:p.Arg1359Leu
XM_011526837.1:c.4172G>T	XP_011525139.1:p.Arg1391Leu
XM_011526838.1:c.3938G>T	XP_011525140.1:p.Arg1313Leu
XM_011526839.1:c.3836G>T	XP_011525141.1:p.Arg1279Leu
XM_011526840.1:c.3179G>T	XP_011525142.1:p.Arg1060Leu
XM_011526841.1:c.2765G>T	XP_011525143.1:p.Arg922Leu
XM_011526842.1:c.2618G>T	XP_011525144.1:p.Arg873Leu
XM_011526843.1:c.1934G>T	XP_011525145.1:p.Arg645Leu
XM_011526844.1:c.1934G>T	XP_011525146.1:p.Arg645Leu
XM_011526840.2:c.3179G>T	XP_011525142.1:p.Arg1060Leu
XM_011526841.2:c.2765G>T	XP_011525143.1:p.Arg922Leu
XM_011526844.2:c.1934G>T	XP_011525146.1:p.Arg645Leu
XM_017026665.1:c.4187G>T	XP_016882154.1:p.Arg1396Leu
NM_001083961.2:c.4187G>T MANE Select	NP_001077430.1:p.Arg1396Leu
NM_173636.5:c.4172G>T	NP_775907.4:p.Arg1391Leu