Canonical Allele Identifier: CA405460903

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595507T>G (hg19) ; chr19:g.36104605T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104605T>G , CM000681.2:g.36104605T>G	GRCh38
NC_000019.9:g.36595507T>G , CM000681.1:g.36595507T>G	GRCh37
NC_000019.8:g.41287347T>G	NCBI36
NG_028101.1:g.54725T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4226T>G	ENSP00000270301.6:p.Leu1409Arg
ENST00000401500.7:c.4241T>G MANE Select	ENSP00000384792.1:p.Leu1414Arg
ENST00000587391.6:c.*4101T>G	ENSP00000465525.1:n.*4101T>G
ENST00000679357.1:c.2321T>G
ENST00000679598.1:c.986T>G
ENST00000679682.1:c.4226T>G	ENSP00000506226.1:p.Leu1409Arg
ENST00000679714.1:c.4235T>G	ENSP00000506627.1:p.Leu1412Arg
ENST00000679757.1:c.3890T>G	ENSP00000505158.1:p.Leu1297Arg
ENST00000679858.1:c.*3623T>G	ENSP00000505655.1:n.*3623T>G
ENST00000680211.1:c.842T>G	ENSP00000506102.1:p.Leu281Arg
ENST00000680280.1:n.1744T>G
ENST00000680349.1:n.2890T>G
ENST00000680403.1:c.4226T>G	ENSP00000505677.1:p.Leu1409Arg
ENST00000680564.1:c.3992T>G	ENSP00000505582.1:p.Leu1331Arg
ENST00000680590.1:c.*2621T>G	ENSP00000505350.1:n.*2621T>G
ENST00000680597.1:c.974T>G
ENST00000680739.1:c.1256T>G
ENST00000680773.1:n.2742T>G
ENST00000680806.1:c.*3544T>G	ENSP00000506418.1:n.*3544T>G
ENST00000680997.1:n.2173T>G
ENST00000681608.1:n.2086T>G
ENST00000681625.1:c.*1573T>G	ENSP00000505555.1:n.*1573T>G
ENST00000681648.1:n.2292T>G
ENST00000270301.11:c.4226T>G	ENSP00000270301.6:p.Leu1409Arg
ENST00000401500.6:c.4241T>G	ENSP00000384792.1:p.Leu1414Arg
ENST00000587391.5:c.*4101T>G	ENSP00000465525.1:n.*4101T>G
NM_001083961.1:c.4241T>G	NP_001077430.1:p.Leu1414Arg
NM_173636.4:c.4226T>G	NP_775907.4:p.Leu1409Arg
XM_005258809.2:c.4130T>G	XP_005258866.1:p.Leu1377Arg
XM_011526837.1:c.4226T>G	XP_011525139.1:p.Leu1409Arg
XM_011526838.1:c.3992T>G	XP_011525140.1:p.Leu1331Arg
XM_011526839.1:c.3890T>G	XP_011525141.1:p.Leu1297Arg
XM_011526840.1:c.3233T>G	XP_011525142.1:p.Leu1078Arg
XM_011526841.1:c.2819T>G	XP_011525143.1:p.Leu940Arg
XM_011526842.1:c.2672T>G	XP_011525144.1:p.Leu891Arg
XM_011526843.1:c.1988T>G	XP_011525145.1:p.Leu663Arg
XM_011526844.1:c.1988T>G	XP_011525146.1:p.Leu663Arg
XM_011526840.2:c.3233T>G	XP_011525142.1:p.Leu1078Arg
XM_011526841.2:c.2819T>G	XP_011525143.1:p.Leu940Arg
XM_011526844.2:c.1988T>G	XP_011525146.1:p.Leu663Arg
XM_017026665.1:c.4241T>G	XP_016882154.1:p.Leu1414Arg
NM_001083961.2:c.4241T>G MANE Select	NP_001077430.1:p.Leu1414Arg
NM_173636.5:c.4226T>G	NP_775907.4:p.Leu1409Arg