Canonical Allele Identifier: CA405460391

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595444G>C (hg19) ; chr19:g.36104542G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4163G>C	ENSP00000270301.6:p.Ser1388Thr
ENST00000401500.7:c.4178G>C MANE Select	ENSP00000384792.1:p.Ser1393Thr
ENST00000587391.6:c.*4038G>C	ENSP00000465525.1:n.*4038G>C
ENST00000679357.1:c.2258G>C
ENST00000679598.1:c.923G>C
ENST00000679682.1:c.4163G>C	ENSP00000506226.1:p.Ser1388Thr
ENST00000679714.1:c.4172G>C	ENSP00000506627.1:p.Ser1391Thr
ENST00000679757.1:c.3827G>C	ENSP00000505158.1:p.Ser1276Thr
ENST00000679858.1:c.*3560G>C	ENSP00000505655.1:n.*3560G>C
ENST00000680211.1:c.779G>C	ENSP00000506102.1:p.Ser260Thr
ENST00000680280.1:n.1681G>C
ENST00000680349.1:n.2827G>C
ENST00000680403.1:c.4163G>C	ENSP00000505677.1:p.Ser1388Thr
ENST00000680564.1:c.3929G>C	ENSP00000505582.1:p.Ser1310Thr
ENST00000680590.1:c.*2558G>C	ENSP00000505350.1:n.*2558G>C
ENST00000680597.1:c.911G>C
ENST00000680739.1:c.1193G>C
ENST00000680773.1:n.2679G>C
ENST00000680806.1:c.*3481G>C	ENSP00000506418.1:n.*3481G>C
ENST00000680997.1:n.2110G>C
ENST00000681608.1:n.2023G>C
ENST00000681625.1:c.*1510G>C	ENSP00000505555.1:n.*1510G>C
ENST00000681648.1:n.2229G>C
ENST00000270301.11:c.4163G>C	ENSP00000270301.6:p.Ser1388Thr
ENST00000401500.6:c.4178G>C	ENSP00000384792.1:p.Ser1393Thr
ENST00000587391.5:c.*4038G>C	ENSP00000465525.1:n.*4038G>C
NM_001083961.1:c.4178G>C	NP_001077430.1:p.Ser1393Thr
NM_173636.4:c.4163G>C	NP_775907.4:p.Ser1388Thr
XM_005258809.2:c.4067G>C	XP_005258866.1:p.Ser1356Thr
XM_011526837.1:c.4163G>C	XP_011525139.1:p.Ser1388Thr
XM_011526838.1:c.3929G>C	XP_011525140.1:p.Ser1310Thr
XM_011526839.1:c.3827G>C	XP_011525141.1:p.Ser1276Thr
XM_011526840.1:c.3170G>C	XP_011525142.1:p.Ser1057Thr
XM_011526841.1:c.2756G>C	XP_011525143.1:p.Ser919Thr
XM_011526842.1:c.2609G>C	XP_011525144.1:p.Ser870Thr
XM_011526843.1:c.1925G>C	XP_011525145.1:p.Ser642Thr
XM_011526844.1:c.1925G>C	XP_011525146.1:p.Ser642Thr
XM_011526840.2:c.3170G>C	XP_011525142.1:p.Ser1057Thr
XM_011526841.2:c.2756G>C	XP_011525143.1:p.Ser919Thr
XM_011526844.2:c.1925G>C	XP_011525146.1:p.Ser642Thr
XM_017026665.1:c.4178G>C	XP_016882154.1:p.Ser1393Thr
NM_001083961.2:c.4178G>C MANE Select	NP_001077430.1:p.Ser1393Thr
NM_173636.5:c.4163G>C	NP_775907.4:p.Ser1388Thr