Canonical Allele Identifier: CA405460353

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595437C>T (hg19) ; chr19:g.36104535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104535C>T , CM000681.2:g.36104535C>T	GRCh38
NC_000019.9:g.36595437C>T , CM000681.1:g.36595437C>T	GRCh37
NC_000019.8:g.41287277C>T	NCBI36
NG_028101.1:g.54655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4156C>T	ENSP00000270301.6:p.Gln1386Ter
ENST00000401500.7:c.4171C>T MANE Select	ENSP00000384792.1:p.Gln1391Ter
ENST00000587391.6:c.*4031C>T	ENSP00000465525.1:n.*4031C>T
ENST00000679357.1:c.2251C>T
ENST00000679598.1:c.919-3C>T
ENST00000679682.1:c.4156C>T	ENSP00000506226.1:p.Gln1386Ter
ENST00000679714.1:c.4165C>T	ENSP00000506627.1:p.Gln1389Ter
ENST00000679757.1:c.3820C>T	ENSP00000505158.1:p.Gln1274Ter
ENST00000679858.1:c.*3553C>T	ENSP00000505655.1:n.*3553C>T
ENST00000680211.1:c.772C>T	ENSP00000506102.1:p.Gln258Ter
ENST00000680280.1:n.1674C>T
ENST00000680349.1:n.2820C>T
ENST00000680403.1:c.4156C>T	ENSP00000505677.1:p.Gln1386Ter
ENST00000680564.1:c.3922C>T	ENSP00000505582.1:p.Gln1308Ter
ENST00000680590.1:c.*2551C>T	ENSP00000505350.1:n.*2551C>T
ENST00000680597.1:c.904C>T
ENST00000680739.1:c.1186C>T
ENST00000680773.1:n.2672C>T
ENST00000680806.1:c.*3474C>T	ENSP00000506418.1:n.*3474C>T
ENST00000680997.1:n.2103C>T
ENST00000681608.1:n.2016C>T
ENST00000681625.1:c.*1503C>T	ENSP00000505555.1:n.*1503C>T
ENST00000681648.1:n.2222C>T
ENST00000270301.11:c.4156C>T	ENSP00000270301.6:p.Gln1386Ter
ENST00000401500.6:c.4171C>T	ENSP00000384792.1:p.Gln1391Ter
ENST00000587391.5:c.*4031C>T	ENSP00000465525.1:n.*4031C>T
NM_001083961.1:c.4171C>T	NP_001077430.1:p.Gln1391Ter
NM_173636.4:c.4156C>T	NP_775907.4:p.Gln1386Ter
XM_005258809.2:c.4060C>T	XP_005258866.1:p.Gln1354Ter
XM_011526837.1:c.4156C>T	XP_011525139.1:p.Gln1386Ter
XM_011526838.1:c.3922C>T	XP_011525140.1:p.Gln1308Ter
XM_011526839.1:c.3820C>T	XP_011525141.1:p.Gln1274Ter
XM_011526840.1:c.3163C>T	XP_011525142.1:p.Gln1055Ter
XM_011526841.1:c.2749C>T	XP_011525143.1:p.Gln917Ter
XM_011526842.1:c.2602C>T	XP_011525144.1:p.Gln868Ter
XM_011526843.1:c.1918C>T	XP_011525145.1:p.Gln640Ter
XM_011526844.1:c.1918C>T	XP_011525146.1:p.Gln640Ter
XM_011526840.2:c.3163C>T	XP_011525142.1:p.Gln1055Ter
XM_011526841.2:c.2749C>T	XP_011525143.1:p.Gln917Ter
XM_011526844.2:c.1918C>T	XP_011525146.1:p.Gln640Ter
XM_017026665.1:c.4171C>T	XP_016882154.1:p.Gln1391Ter
NM_001083961.2:c.4171C>T MANE Select	NP_001077430.1:p.Gln1391Ter
NM_173636.5:c.4156C>T	NP_775907.4:p.Gln1386Ter