Canonical Allele Identifier: CA405460943

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595512A>T (hg19) ; chr19:g.36104610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104610A>T , CM000681.2:g.36104610A>T	GRCh38
NC_000019.9:g.36595512A>T , CM000681.1:g.36595512A>T	GRCh37
NC_000019.8:g.41287352A>T	NCBI36
NG_028101.1:g.54730A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4231A>T	ENSP00000270301.6:p.Arg1411Trp
ENST00000401500.7:c.4246A>T MANE Select	ENSP00000384792.1:p.Arg1416Trp
ENST00000587391.6:c.*4106A>T	ENSP00000465525.1:n.*4106A>T
ENST00000679357.1:c.2326A>T
ENST00000679598.1:c.991A>T
ENST00000679682.1:c.4231A>T	ENSP00000506226.1:p.Arg1411Trp
ENST00000679714.1:c.4240A>T	ENSP00000506627.1:p.Arg1414Trp
ENST00000679757.1:c.3895A>T	ENSP00000505158.1:p.Arg1299Trp
ENST00000679858.1:c.*3628A>T	ENSP00000505655.1:n.*3628A>T
ENST00000680211.1:c.847A>T	ENSP00000506102.1:p.Arg283Trp
ENST00000680280.1:n.1749A>T
ENST00000680349.1:n.2895A>T
ENST00000680403.1:c.4231A>T	ENSP00000505677.1:p.Arg1411Trp
ENST00000680564.1:c.3997A>T	ENSP00000505582.1:p.Arg1333Trp
ENST00000680590.1:c.*2626A>T	ENSP00000505350.1:n.*2626A>T
ENST00000680597.1:c.979A>T
ENST00000680739.1:c.1261A>T
ENST00000680773.1:n.2747A>T
ENST00000680806.1:c.*3549A>T	ENSP00000506418.1:n.*3549A>T
ENST00000680997.1:n.2178A>T
ENST00000681608.1:n.2091A>T
ENST00000681625.1:c.*1578A>T	ENSP00000505555.1:n.*1578A>T
ENST00000681648.1:n.2297A>T
ENST00000270301.11:c.4231A>T	ENSP00000270301.6:p.Arg1411Trp
ENST00000401500.6:c.4246A>T	ENSP00000384792.1:p.Arg1416Trp
ENST00000587391.5:c.*4106A>T	ENSP00000465525.1:n.*4106A>T
NM_001083961.1:c.4246A>T	NP_001077430.1:p.Arg1416Trp
NM_173636.4:c.4231A>T	NP_775907.4:p.Arg1411Trp
XM_005258809.2:c.4135A>T	XP_005258866.1:p.Arg1379Trp
XM_011526837.1:c.4231A>T	XP_011525139.1:p.Arg1411Trp
XM_011526838.1:c.3997A>T	XP_011525140.1:p.Arg1333Trp
XM_011526839.1:c.3895A>T	XP_011525141.1:p.Arg1299Trp
XM_011526840.1:c.3238A>T	XP_011525142.1:p.Arg1080Trp
XM_011526841.1:c.2824A>T	XP_011525143.1:p.Arg942Trp
XM_011526842.1:c.2677A>T	XP_011525144.1:p.Arg893Trp
XM_011526843.1:c.1993A>T	XP_011525145.1:p.Arg665Trp
XM_011526844.1:c.1993A>T	XP_011525146.1:p.Arg665Trp
XM_011526840.2:c.3238A>T	XP_011525142.1:p.Arg1080Trp
XM_011526841.2:c.2824A>T	XP_011525143.1:p.Arg942Trp
XM_011526844.2:c.1993A>T	XP_011525146.1:p.Arg665Trp
XM_017026665.1:c.4246A>T	XP_016882154.1:p.Arg1416Trp
NM_001083961.2:c.4246A>T MANE Select	NP_001077430.1:p.Arg1416Trp
NM_173636.5:c.4231A>T	NP_775907.4:p.Arg1411Trp