Canonical Allele Identifier: CA2333972212

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104606G= , CM000681.2:g.36104606G=	GRCh38
NC_000019.9:g.36595508G= , CM000681.1:g.36595508G=	GRCh37
NC_000019.8:g.41287348G=	NCBI36
NG_028101.1:g.54726G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4227G=	ENSP00000270301.6:p.Leu1409=
ENST00000401500.7:c.4242G= MANE Select	ENSP00000384792.1:p.Leu1414=
ENST00000587391.6:c.*4102G=	ENSP00000465525.1:n.*4102G=
ENST00000679357.1:c.2322G=
ENST00000679598.1:c.987G=
ENST00000679682.1:c.4227G=	ENSP00000506226.1:p.Leu1409=
ENST00000679714.1:c.4236G=	ENSP00000506627.1:p.Leu1412=
ENST00000679757.1:c.3891G=	ENSP00000505158.1:p.Leu1297=
ENST00000679858.1:c.*3624G=	ENSP00000505655.1:n.*3624G=
ENST00000680211.1:c.843G=	ENSP00000506102.1:p.Leu281=
ENST00000680280.1:n.1745G=
ENST00000680349.1:n.2891G=
ENST00000680403.1:c.4227G=	ENSP00000505677.1:p.Leu1409=
ENST00000680564.1:c.3993G=	ENSP00000505582.1:p.Leu1331=
ENST00000680590.1:c.*2622G=	ENSP00000505350.1:n.*2622G=
ENST00000680597.1:c.975G=
ENST00000680739.1:c.1257G=
ENST00000680773.1:n.2743G=
ENST00000680806.1:c.*3545G=	ENSP00000506418.1:n.*3545G=
ENST00000680997.1:n.2174G=
ENST00000681608.1:n.2087G=
ENST00000681625.1:c.*1574G=	ENSP00000505555.1:n.*1574G=
ENST00000681648.1:n.2293G=
ENST00000270301.11:c.4227G=	ENSP00000270301.6:p.Leu1409=
ENST00000401500.6:c.4242G=	ENSP00000384792.1:p.Leu1414=
ENST00000587391.5:c.*4102G=	ENSP00000465525.1:n.*4102G=
NM_001083961.1:c.4242G=	NP_001077430.1:p.Leu1414=
NM_173636.4:c.4227G=	NP_775907.4:p.Leu1409=
XM_005258809.2:c.4131G=	XP_005258866.1:p.Leu1377=
XM_011526837.1:c.4227G=	XP_011525139.1:p.Leu1409=
XM_011526838.1:c.3993G=	XP_011525140.1:p.Leu1331=
XM_011526839.1:c.3891G=	XP_011525141.1:p.Leu1297=
XM_011526840.1:c.3234G=	XP_011525142.1:p.Leu1078=
XM_011526841.1:c.2820G=	XP_011525143.1:p.Leu940=
XM_011526842.1:c.2673G=	XP_011525144.1:p.Leu891=
XM_011526843.1:c.1989G=	XP_011525145.1:p.Leu663=
XM_011526844.1:c.1989G=	XP_011525146.1:p.Leu663=
XM_011526840.2:c.3234G=	XP_011525142.1:p.Leu1078=
XM_011526841.2:c.2820G=	XP_011525143.1:p.Leu940=
XM_011526844.2:c.1989G=	XP_011525146.1:p.Leu663=
XM_017026665.1:c.4242G=	XP_016882154.1:p.Leu1414=
NM_001083961.2:c.4242G= MANE Select	NP_001077430.1:p.Leu1414=
NM_173636.5:c.4227G=	NP_775907.4:p.Leu1409=