Canonical Allele Identifier: CA405460307

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595426T>G (hg19) ; chr19:g.36104524T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104524T>G , CM000681.2:g.36104524T>G	GRCh38
NC_000019.9:g.36595426T>G , CM000681.1:g.36595426T>G	GRCh37
NC_000019.8:g.41287266T>G	NCBI36
NG_028101.1:g.54644T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4145T>G	ENSP00000270301.6:p.Leu1382Arg
ENST00000401500.7:c.4160T>G MANE Select	ENSP00000384792.1:p.Leu1387Arg
ENST00000587391.6:c.*4020T>G	ENSP00000465525.1:n.*4020T>G
ENST00000679357.1:c.2240T>G
ENST00000679598.1:c.919-14T>G
ENST00000679682.1:c.4145T>G	ENSP00000506226.1:p.Leu1382Arg
ENST00000679714.1:c.4154T>G	ENSP00000506627.1:p.Leu1385Arg
ENST00000679757.1:c.3809T>G	ENSP00000505158.1:p.Leu1270Arg
ENST00000679858.1:c.*3542T>G	ENSP00000505655.1:n.*3542T>G
ENST00000680211.1:c.761T>G	ENSP00000506102.1:p.Leu254Arg
ENST00000680280.1:n.1663T>G
ENST00000680349.1:n.2809T>G
ENST00000680403.1:c.4145T>G	ENSP00000505677.1:p.Leu1382Arg
ENST00000680564.1:c.3911T>G	ENSP00000505582.1:p.Leu1304Arg
ENST00000680590.1:c.*2540T>G	ENSP00000505350.1:n.*2540T>G
ENST00000680597.1:c.893T>G
ENST00000680739.1:c.1175T>G
ENST00000680773.1:n.2661T>G
ENST00000680806.1:c.*3463T>G	ENSP00000506418.1:n.*3463T>G
ENST00000680997.1:n.2092T>G
ENST00000681608.1:n.2005T>G
ENST00000681625.1:c.*1492T>G	ENSP00000505555.1:n.*1492T>G
ENST00000681648.1:n.2211T>G
ENST00000270301.11:c.4145T>G	ENSP00000270301.6:p.Leu1382Arg
ENST00000401500.6:c.4160T>G	ENSP00000384792.1:p.Leu1387Arg
ENST00000587391.5:c.*4020T>G	ENSP00000465525.1:n.*4020T>G
NM_001083961.1:c.4160T>G	NP_001077430.1:p.Leu1387Arg
NM_173636.4:c.4145T>G	NP_775907.4:p.Leu1382Arg
XM_005258809.2:c.4049T>G	XP_005258866.1:p.Leu1350Arg
XM_011526837.1:c.4145T>G	XP_011525139.1:p.Leu1382Arg
XM_011526838.1:c.3911T>G	XP_011525140.1:p.Leu1304Arg
XM_011526839.1:c.3809T>G	XP_011525141.1:p.Leu1270Arg
XM_011526840.1:c.3152T>G	XP_011525142.1:p.Leu1051Arg
XM_011526841.1:c.2738T>G	XP_011525143.1:p.Leu913Arg
XM_011526842.1:c.2591T>G	XP_011525144.1:p.Leu864Arg
XM_011526843.1:c.1907T>G	XP_011525145.1:p.Leu636Arg
XM_011526844.1:c.1907T>G	XP_011525146.1:p.Leu636Arg
XM_011526840.2:c.3152T>G	XP_011525142.1:p.Leu1051Arg
XM_011526841.2:c.2738T>G	XP_011525143.1:p.Leu913Arg
XM_011526844.2:c.1907T>G	XP_011525146.1:p.Leu636Arg
XM_017026665.1:c.4160T>G	XP_016882154.1:p.Leu1387Arg
NM_001083961.2:c.4160T>G MANE Select	NP_001077430.1:p.Leu1387Arg
NM_173636.5:c.4145T>G	NP_775907.4:p.Leu1382Arg