Canonical Allele Identifier: CA9396312

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103208G>A , CM000681.2:g.36103208G>A	GRCh38
NC_000019.9:g.36594110G>A , CM000681.1:g.36594110G>A	GRCh37
NC_000019.8:g.41285950G>A	NCBI36
NG_028101.1:g.53328G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3499+1G>A	ENSP00000270301.6:n.3499+1G>A
ENST00000401500.7:c.3514+1G>A MANE Select	ENSP00000384792.1:n.3514+1G>A
ENST00000587391.6:c.*3374+1G>A	ENSP00000465525.1:n.*3374+1G>A
ENST00000679357.1:c.1594+1G>A
ENST00000679598.1:c.279+1G>A
ENST00000679682.1:c.3499+1G>A	ENSP00000506226.1:n.3499+1G>A
ENST00000679714.1:c.3508+1G>A	ENSP00000506627.1:n.3508+1G>A
ENST00000679757.1:c.3163+1G>A	ENSP00000505158.1:n.3163+1G>A
ENST00000679858.1:c.*2896+1G>A	ENSP00000505655.1:n.*2896+1G>A
ENST00000680211.1:c.115+1G>A	ENSP00000506102.1:n.115+1G>A
ENST00000680280.1:n.883G>A
ENST00000680349.1:n.2163+1G>A
ENST00000680403.1:c.3499+1G>A	ENSP00000505677.1:n.3499+1G>A
ENST00000680564.1:c.3265+1G>A	ENSP00000505582.1:n.3265+1G>A
ENST00000680590.1:c.*1894+1G>A	ENSP00000505350.1:n.*1894+1G>A
ENST00000680597.1:c.247+1G>A
ENST00000680739.1:c.529+1G>A
ENST00000680773.1:n.2015+1G>A
ENST00000680806.1:c.*2817+1G>A	ENSP00000506418.1:n.*2817+1G>A
ENST00000680997.1:n.1446+1G>A
ENST00000681608.1:n.1225G>A
ENST00000681625.1:c.*846+1G>A	ENSP00000505555.1:n.*846+1G>A
ENST00000681648.1:n.895G>A
ENST00000270301.11:c.3499+1G>A	ENSP00000270301.6:n.3499+1G>A
ENST00000401500.6:c.3514+1G>A	ENSP00000384792.1:n.3514+1G>A
ENST00000587391.5:c.*3374+1G>A	ENSP00000465525.1:n.*3374+1G>A
NM_001083961.1:c.3514+1G>A	NP_001077430.1:n.3514+1G>A
NM_173636.4:c.3499+1G>A	NP_775907.4:n.3499+1G>A
XM_005258809.2:c.3403+1G>A	XP_005258866.1:n.3403+1G>A
XM_011526837.1:c.3499+1G>A	XP_011525139.1:n.3499+1G>A
XM_011526838.1:c.3265+1G>A	XP_011525140.1:n.3265+1G>A
XM_011526839.1:c.3163+1G>A	XP_011525141.1:n.3163+1G>A
XM_011526840.1:c.2506+1G>A	XP_011525142.1:n.2506+1G>A
XM_011526841.1:c.2092+1G>A	XP_011525143.1:n.2092+1G>A
XM_011526842.1:c.1945+1G>A	XP_011525144.1:n.1945+1G>A
XM_011526843.1:c.1261+1G>A	XP_011525145.1:n.1261+1G>A
XM_011526844.1:c.1261+1G>A	XP_011525146.1:n.1261+1G>A
XM_011526840.2:c.2506+1G>A	XP_011525142.1:n.2506+1G>A
XM_011526841.2:c.2092+1G>A	XP_011525143.1:n.2092+1G>A
XM_011526844.2:c.1261+1G>A	XP_011525146.1:n.1261+1G>A
XM_017026665.1:c.3514+1G>A	XP_016882154.1:n.3514+1G>A
NM_001083961.2:c.3514+1G>A MANE Select	NP_001077430.1:n.3514+1G>A
NM_173636.5:c.3499+1G>A	NP_775907.4:n.3499+1G>A