Canonical Allele Identifier: CA307843125

Gene: WDR62

Linked Data

• dbSNP Id: rs919912208
• MyVariant Identifiers: chr19:g.36595536C>T (hg19) ; chr19:g.36104634C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104634C>T , CM000681.2:g.36104634C>T	GRCh38
NC_000019.9:g.36595536C>T , CM000681.1:g.36595536C>T	GRCh37
NC_000019.8:g.41287376C>T	NCBI36
NG_028101.1:g.54754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4255C>T	ENSP00000270301.6:p.Leu1419=
ENST00000401500.7:c.4270C>T MANE Select	ENSP00000384792.1:p.Leu1424=
ENST00000587391.6:c.*4130C>T	ENSP00000465525.1:n.*4130C>T
ENST00000679357.1:c.2350C>T
ENST00000679598.1:c.1015C>T
ENST00000679682.1:c.4255C>T	ENSP00000506226.1:p.Leu1419=
ENST00000679714.1:c.4264C>T	ENSP00000506627.1:p.Leu1422=
ENST00000679757.1:c.3919C>T	ENSP00000505158.1:p.Leu1307=
ENST00000679858.1:c.*3652C>T	ENSP00000505655.1:n.*3652C>T
ENST00000680211.1:c.871C>T	ENSP00000506102.1:p.Leu291=
ENST00000680280.1:n.1773C>T
ENST00000680349.1:n.2919C>T
ENST00000680403.1:c.4255C>T	ENSP00000505677.1:p.Leu1419=
ENST00000680564.1:c.4021C>T	ENSP00000505582.1:p.Leu1341=
ENST00000680590.1:c.*2650C>T	ENSP00000505350.1:n.*2650C>T
ENST00000680597.1:c.1003C>T
ENST00000680739.1:c.1285C>T
ENST00000680773.1:n.2771C>T
ENST00000680806.1:c.*3573C>T	ENSP00000506418.1:n.*3573C>T
ENST00000680997.1:n.2202C>T
ENST00000681608.1:n.2115C>T
ENST00000681625.1:c.*1602C>T	ENSP00000505555.1:n.*1602C>T
ENST00000681648.1:n.2321C>T
ENST00000270301.11:c.4255C>T	ENSP00000270301.6:p.Leu1419=
ENST00000401500.6:c.4270C>T	ENSP00000384792.1:p.Leu1424=
ENST00000587391.5:c.*4130C>T	ENSP00000465525.1:n.*4130C>T
NM_001083961.1:c.4270C>T	NP_001077430.1:p.Leu1424=
NM_173636.4:c.4255C>T	NP_775907.4:p.Leu1419=
XM_005258809.2:c.4159C>T	XP_005258866.1:p.Leu1387=
XM_011526837.1:c.4255C>T	XP_011525139.1:p.Leu1419=
XM_011526838.1:c.4021C>T	XP_011525140.1:p.Leu1341=
XM_011526839.1:c.3919C>T	XP_011525141.1:p.Leu1307=
XM_011526840.1:c.3262C>T	XP_011525142.1:p.Leu1088=
XM_011526841.1:c.2848C>T	XP_011525143.1:p.Leu950=
XM_011526842.1:c.2701C>T	XP_011525144.1:p.Leu901=
XM_011526843.1:c.2017C>T	XP_011525145.1:p.Leu673=
XM_011526844.1:c.2017C>T	XP_011525146.1:p.Leu673=
XM_011526840.2:c.3262C>T	XP_011525142.1:p.Leu1088=
XM_011526841.2:c.2848C>T	XP_011525143.1:p.Leu950=
XM_011526844.2:c.2017C>T	XP_011525146.1:p.Leu673=
XM_017026665.1:c.4270C>T	XP_016882154.1:p.Leu1424=
NM_001083961.2:c.4270C>T MANE Select	NP_001077430.1:p.Leu1424=
NM_173636.5:c.4255C>T	NP_775907.4:p.Leu1419=