Canonical Allele Identifier: CA9395807

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36090486A>G , CM000681.2:g.36090486A>G	GRCh38
NC_000019.9:g.36581388A>G , CM000681.1:g.36581388A>G	GRCh37
NC_000019.8:g.41273228A>G	NCBI36
NG_028101.1:g.40606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.2000A>G	ENSP00000270301.6:p.Lys667Arg
ENST00000401500.7:c.2000A>G MANE Select	ENSP00000384792.1:p.Lys667Arg
ENST00000587391.6:c.*690A>G	ENSP00000465525.1:n.*690A>G
ENST00000679489.1:c.318A>G
ENST00000679682.1:c.1985A>G	ENSP00000506226.1:p.Lys662Arg
ENST00000679714.1:c.1994A>G	ENSP00000506627.1:p.Lys665Arg
ENST00000679757.1:c.1649A>G	ENSP00000505158.1:p.Lys550Arg
ENST00000679858.1:c.*797A>G	ENSP00000505655.1:n.*797A>G
ENST00000680377.1:c.450A>G
ENST00000680403.1:c.2000A>G	ENSP00000505677.1:p.Lys667Arg
ENST00000680489.1:n.2323A>G
ENST00000680564.1:c.2000A>G	ENSP00000505582.1:p.Lys667Arg
ENST00000680590.1:c.*399A>G	ENSP00000505350.1:n.*399A>G
ENST00000680806.1:c.*829A>G	ENSP00000506418.1:n.*829A>G
ENST00000680858.1:c.408+1180A>G
ENST00000681302.1:c.450A>G
ENST00000681625.1:c.1985A>G	ENSP00000505555.1:p.Lys662Arg
ENST00000270301.11:c.2000A>G	ENSP00000270301.6:p.Lys667Arg
ENST00000401500.6:c.2000A>G	ENSP00000384792.1:p.Lys667Arg
ENST00000587391.5:c.*690A>G	ENSP00000465525.1:n.*690A>G
NM_001083961.1:c.2000A>G	NP_001077430.1:p.Lys667Arg
NM_173636.4:c.2000A>G	NP_775907.4:p.Lys667Arg
XM_005258809.2:c.2000A>G	XP_005258866.1:p.Lys667Arg
XM_011526837.1:c.1985A>G	XP_011525139.1:p.Lys662Arg
XM_011526838.1:c.2000A>G	XP_011525140.1:p.Lys667Arg
XM_011526839.1:c.1649A>G	XP_011525141.1:p.Lys550Arg
XM_011526840.1:c.992A>G	XP_011525142.1:p.Lys331Arg
XM_011526841.1:c.578A>G	XP_011525143.1:p.Lys193Arg
XM_011526842.1:c.431A>G	XP_011525144.1:p.Lys144Arg
XM_011526843.1:c.-78A>G	XP_011525145.1:n.-78A>G
XM_011526840.2:c.992A>G	XP_011525142.1:p.Lys331Arg
XM_011526841.2:c.578A>G	XP_011525143.1:p.Lys193Arg
XM_017026665.1:c.2000A>G	XP_016882154.1:p.Lys667Arg
XR_001753671.1:n.2091A>G
XR_001753672.1:n.2091A>G
NM_001083961.2:c.2000A>G MANE Select	NP_001077430.1:p.Lys667Arg
NM_173636.5:c.2000A>G	NP_775907.4:p.Lys667Arg