Canonical Allele Identifier: CA405460373

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595440G>T (hg19) ; chr19:g.36104538G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104538G>T , CM000681.2:g.36104538G>T	GRCh38
NC_000019.9:g.36595440G>T , CM000681.1:g.36595440G>T	GRCh37
NC_000019.8:g.41287280G>T	NCBI36
NG_028101.1:g.54658G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4159G>T	ENSP00000270301.6:p.Gly1387Cys
ENST00000401500.7:c.4174G>T MANE Select	ENSP00000384792.1:p.Gly1392Cys
ENST00000587391.6:c.*4034G>T	ENSP00000465525.1:n.*4034G>T
ENST00000679357.1:c.2254G>T
ENST00000679598.1:c.919G>T
ENST00000679682.1:c.4159G>T	ENSP00000506226.1:p.Gly1387Cys
ENST00000679714.1:c.4168G>T	ENSP00000506627.1:p.Gly1390Cys
ENST00000679757.1:c.3823G>T	ENSP00000505158.1:p.Gly1275Cys
ENST00000679858.1:c.*3556G>T	ENSP00000505655.1:n.*3556G>T
ENST00000680211.1:c.775G>T	ENSP00000506102.1:p.Gly259Cys
ENST00000680280.1:n.1677G>T
ENST00000680349.1:n.2823G>T
ENST00000680403.1:c.4159G>T	ENSP00000505677.1:p.Gly1387Cys
ENST00000680564.1:c.3925G>T	ENSP00000505582.1:p.Gly1309Cys
ENST00000680590.1:c.*2554G>T	ENSP00000505350.1:n.*2554G>T
ENST00000680597.1:c.907G>T
ENST00000680739.1:c.1189G>T
ENST00000680773.1:n.2675G>T
ENST00000680806.1:c.*3477G>T	ENSP00000506418.1:n.*3477G>T
ENST00000680997.1:n.2106G>T
ENST00000681608.1:n.2019G>T
ENST00000681625.1:c.*1506G>T	ENSP00000505555.1:n.*1506G>T
ENST00000681648.1:n.2225G>T
ENST00000270301.11:c.4159G>T	ENSP00000270301.6:p.Gly1387Cys
ENST00000401500.6:c.4174G>T	ENSP00000384792.1:p.Gly1392Cys
ENST00000587391.5:c.*4034G>T	ENSP00000465525.1:n.*4034G>T
NM_001083961.1:c.4174G>T	NP_001077430.1:p.Gly1392Cys
NM_173636.4:c.4159G>T	NP_775907.4:p.Gly1387Cys
XM_005258809.2:c.4063G>T	XP_005258866.1:p.Gly1355Cys
XM_011526837.1:c.4159G>T	XP_011525139.1:p.Gly1387Cys
XM_011526838.1:c.3925G>T	XP_011525140.1:p.Gly1309Cys
XM_011526839.1:c.3823G>T	XP_011525141.1:p.Gly1275Cys
XM_011526840.1:c.3166G>T	XP_011525142.1:p.Gly1056Cys
XM_011526841.1:c.2752G>T	XP_011525143.1:p.Gly918Cys
XM_011526842.1:c.2605G>T	XP_011525144.1:p.Gly869Cys
XM_011526843.1:c.1921G>T	XP_011525145.1:p.Gly641Cys
XM_011526844.1:c.1921G>T	XP_011525146.1:p.Gly641Cys
XM_011526840.2:c.3166G>T	XP_011525142.1:p.Gly1056Cys
XM_011526841.2:c.2752G>T	XP_011525143.1:p.Gly918Cys
XM_011526844.2:c.1921G>T	XP_011525146.1:p.Gly641Cys
XM_017026665.1:c.4174G>T	XP_016882154.1:p.Gly1392Cys
NM_001083961.2:c.4174G>T MANE Select	NP_001077430.1:p.Gly1392Cys
NM_173636.5:c.4159G>T	NP_775907.4:p.Gly1387Cys