Canonical Allele Identifier: CA405460332

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595431C>G (hg19) ; chr19:g.36104529C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104529C>G , CM000681.2:g.36104529C>G	GRCh38
NC_000019.9:g.36595431C>G , CM000681.1:g.36595431C>G	GRCh37
NC_000019.8:g.41287271C>G	NCBI36
NG_028101.1:g.54649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4150C>G	ENSP00000270301.6:p.Leu1384Val
ENST00000401500.7:c.4165C>G MANE Select	ENSP00000384792.1:p.Leu1389Val
ENST00000587391.6:c.*4025C>G	ENSP00000465525.1:n.*4025C>G
ENST00000679357.1:c.2245C>G
ENST00000679598.1:c.919-9C>G
ENST00000679682.1:c.4150C>G	ENSP00000506226.1:p.Leu1384Val
ENST00000679714.1:c.4159C>G	ENSP00000506627.1:p.Leu1387Val
ENST00000679757.1:c.3814C>G	ENSP00000505158.1:p.Leu1272Val
ENST00000679858.1:c.*3547C>G	ENSP00000505655.1:n.*3547C>G
ENST00000680211.1:c.766C>G	ENSP00000506102.1:p.Leu256Val
ENST00000680280.1:n.1668C>G
ENST00000680349.1:n.2814C>G
ENST00000680403.1:c.4150C>G	ENSP00000505677.1:p.Leu1384Val
ENST00000680564.1:c.3916C>G	ENSP00000505582.1:p.Leu1306Val
ENST00000680590.1:c.*2545C>G	ENSP00000505350.1:n.*2545C>G
ENST00000680597.1:c.898C>G
ENST00000680739.1:c.1180C>G
ENST00000680773.1:n.2666C>G
ENST00000680806.1:c.*3468C>G	ENSP00000506418.1:n.*3468C>G
ENST00000680997.1:n.2097C>G
ENST00000681608.1:n.2010C>G
ENST00000681625.1:c.*1497C>G	ENSP00000505555.1:n.*1497C>G
ENST00000681648.1:n.2216C>G
ENST00000270301.11:c.4150C>G	ENSP00000270301.6:p.Leu1384Val
ENST00000401500.6:c.4165C>G	ENSP00000384792.1:p.Leu1389Val
ENST00000587391.5:c.*4025C>G	ENSP00000465525.1:n.*4025C>G
NM_001083961.1:c.4165C>G	NP_001077430.1:p.Leu1389Val
NM_173636.4:c.4150C>G	NP_775907.4:p.Leu1384Val
XM_005258809.2:c.4054C>G	XP_005258866.1:p.Leu1352Val
XM_011526837.1:c.4150C>G	XP_011525139.1:p.Leu1384Val
XM_011526838.1:c.3916C>G	XP_011525140.1:p.Leu1306Val
XM_011526839.1:c.3814C>G	XP_011525141.1:p.Leu1272Val
XM_011526840.1:c.3157C>G	XP_011525142.1:p.Leu1053Val
XM_011526841.1:c.2743C>G	XP_011525143.1:p.Leu915Val
XM_011526842.1:c.2596C>G	XP_011525144.1:p.Leu866Val
XM_011526843.1:c.1912C>G	XP_011525145.1:p.Leu638Val
XM_011526844.1:c.1912C>G	XP_011525146.1:p.Leu638Val
XM_011526840.2:c.3157C>G	XP_011525142.1:p.Leu1053Val
XM_011526841.2:c.2743C>G	XP_011525143.1:p.Leu915Val
XM_011526844.2:c.1912C>G	XP_011525146.1:p.Leu638Val
XM_017026665.1:c.4165C>G	XP_016882154.1:p.Leu1389Val
NM_001083961.2:c.4165C>G MANE Select	NP_001077430.1:p.Leu1389Val
NM_173636.5:c.4150C>G	NP_775907.4:p.Leu1384Val