Canonical Allele Identifier: CA9396496

Gene: WDR62

Linked Data

• dbSNP Id: rs766250353
• ExAC: 19:36595444 G / T
• gnomAD v2: 19-36595444-G-T
• gnomAD v4: 19-36104542-G-T
• MyVariant Identifiers: chr19:g.36595444G>T (hg19) ; chr19:g.36104542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104542G>T , CM000681.2:g.36104542G>T	GRCh38
NC_000019.9:g.36595444G>T , CM000681.1:g.36595444G>T	GRCh37
NC_000019.8:g.41287284G>T	NCBI36
NG_028101.1:g.54662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4163G>T	ENSP00000270301.6:p.Ser1388Ile
ENST00000401500.7:c.4178G>T MANE Select	ENSP00000384792.1:p.Ser1393Ile
ENST00000587391.6:c.*4038G>T	ENSP00000465525.1:n.*4038G>T
ENST00000679357.1:c.2258G>T
ENST00000679598.1:c.923G>T
ENST00000679682.1:c.4163G>T	ENSP00000506226.1:p.Ser1388Ile
ENST00000679714.1:c.4172G>T	ENSP00000506627.1:p.Ser1391Ile
ENST00000679757.1:c.3827G>T	ENSP00000505158.1:p.Ser1276Ile
ENST00000679858.1:c.*3560G>T	ENSP00000505655.1:n.*3560G>T
ENST00000680211.1:c.779G>T	ENSP00000506102.1:p.Ser260Ile
ENST00000680280.1:n.1681G>T
ENST00000680349.1:n.2827G>T
ENST00000680403.1:c.4163G>T	ENSP00000505677.1:p.Ser1388Ile
ENST00000680564.1:c.3929G>T	ENSP00000505582.1:p.Ser1310Ile
ENST00000680590.1:c.*2558G>T	ENSP00000505350.1:n.*2558G>T
ENST00000680597.1:c.911G>T
ENST00000680739.1:c.1193G>T
ENST00000680773.1:n.2679G>T
ENST00000680806.1:c.*3481G>T	ENSP00000506418.1:n.*3481G>T
ENST00000680997.1:n.2110G>T
ENST00000681608.1:n.2023G>T
ENST00000681625.1:c.*1510G>T	ENSP00000505555.1:n.*1510G>T
ENST00000681648.1:n.2229G>T
ENST00000270301.11:c.4163G>T	ENSP00000270301.6:p.Ser1388Ile
ENST00000401500.6:c.4178G>T	ENSP00000384792.1:p.Ser1393Ile
ENST00000587391.5:c.*4038G>T	ENSP00000465525.1:n.*4038G>T
NM_001083961.1:c.4178G>T	NP_001077430.1:p.Ser1393Ile
NM_173636.4:c.4163G>T	NP_775907.4:p.Ser1388Ile
XM_005258809.2:c.4067G>T	XP_005258866.1:p.Ser1356Ile
XM_011526837.1:c.4163G>T	XP_011525139.1:p.Ser1388Ile
XM_011526838.1:c.3929G>T	XP_011525140.1:p.Ser1310Ile
XM_011526839.1:c.3827G>T	XP_011525141.1:p.Ser1276Ile
XM_011526840.1:c.3170G>T	XP_011525142.1:p.Ser1057Ile
XM_011526841.1:c.2756G>T	XP_011525143.1:p.Ser919Ile
XM_011526842.1:c.2609G>T	XP_011525144.1:p.Ser870Ile
XM_011526843.1:c.1925G>T	XP_011525145.1:p.Ser642Ile
XM_011526844.1:c.1925G>T	XP_011525146.1:p.Ser642Ile
XM_011526840.2:c.3170G>T	XP_011525142.1:p.Ser1057Ile
XM_011526841.2:c.2756G>T	XP_011525143.1:p.Ser919Ile
XM_011526844.2:c.1925G>T	XP_011525146.1:p.Ser642Ile
XM_017026665.1:c.4178G>T	XP_016882154.1:p.Ser1393Ile
NM_001083961.2:c.4178G>T MANE Select	NP_001077430.1:p.Ser1393Ile
NM_173636.5:c.4163G>T	NP_775907.4:p.Ser1388Ile