Canonical Allele Identifier: CA632787346

Gene: WDR62

Linked Data

• dbSNP Id: rs1345551552
• gnomAD v2: 19-36592999-CAGG-C
• gnomAD v3: 19-36102097-CAGG-C
• gnomAD v4: 19-36102097-CAGG-C
• COSMIC: COSM5056562
• MyVariant Identifiers: chr19:g.36593000_36593002del (hg19) ; chr19:g.36102098_36102100del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102100_36102102del , CM000681.2:g.36102100_36102102del	GRCh38
NC_000019.9:g.36593002_36593004del , CM000681.1:g.36593002_36593004del	GRCh37
NC_000019.8:g.41284842_41284844del	NCBI36
NG_028101.1:g.52220_52222del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3169_3171del	ENSP00000270301.6:p.Glu1057del
ENST00000401500.7:c.3169_3171del MANE Select	ENSP00000384792.1:p.Glu1057del
ENST00000587391.6:c.*2444_*2446del	ENSP00000465525.1:n.*2444_*2446del
ENST00000679357.1:c.959_961del
ENST00000679422.1:c.848_850del
ENST00000679682.1:c.3154_3156del	ENSP00000506226.1:p.Glu1052del
ENST00000679714.1:c.3163_3165del	ENSP00000506627.1:p.Glu1055del
ENST00000679757.1:c.2818_2820del	ENSP00000505158.1:p.Glu940del
ENST00000679858.1:c.*2551_*2553del	ENSP00000505655.1:n.*2551_*2553del
ENST00000680211.1:c.-231_-229del	ENSP00000506102.1:n.-231_-229del
ENST00000680349.1:n.1152_1154del
ENST00000680403.1:c.3169_3171del	ENSP00000505677.1:p.Glu1057del
ENST00000680564.1:c.2972-637_2972-635del	ENSP00000505582.1:n.2972-637_2972-635del
ENST00000680590.1:c.*1564_*1566del	ENSP00000505350.1:n.*1564_*1566del
ENST00000680739.1:c.87_89del
ENST00000680773.1:n.1085_1087del
ENST00000680806.1:c.*1887_*1889del	ENSP00000506418.1:n.*1887_*1889del
ENST00000680997.1:n.516_518del
ENST00000681088.1:c.831_833del
ENST00000681608.1:n.117_119del
ENST00000681625.1:c.*501_*503del	ENSP00000505555.1:n.*501_*503del
ENST00000270301.11:c.3169_3171del	ENSP00000270301.6:p.Glu1057del
ENST00000401500.6:c.3169_3171del	ENSP00000384792.1:p.Glu1057del
ENST00000587391.5:c.*2444_*2446del	ENSP00000465525.1:n.*2444_*2446del
NM_001083961.1:c.3169_3171del	NP_001077430.1:p.Glu1057del
NM_173636.4:c.3169_3171del	NP_775907.4:p.Glu1057del
XM_005258809.2:c.3058_3060del	XP_005258866.1:p.Glu1020del
XM_011526837.1:c.3154_3156del	XP_011525139.1:p.Glu1052del
XM_011526838.1:c.2972-637_2972-635del	XP_011525140.1:n.2972-637_2972-635del
XM_011526839.1:c.2818_2820del	XP_011525141.1:p.Glu940del
XM_011526840.1:c.2161_2163del	XP_011525142.1:p.Glu721del
XM_011526841.1:c.1747_1749del	XP_011525143.1:p.Glu583del
XM_011526842.1:c.1600_1602del	XP_011525144.1:p.Glu534del
XM_011526843.1:c.916_918del	XP_011525145.1:p.Glu306del
XM_011526844.1:c.916_918del	XP_011525146.1:p.Glu306del
XM_011526840.2:c.2161_2163del	XP_011525142.1:p.Glu721del
XM_011526841.2:c.1747_1749del	XP_011525143.1:p.Glu583del
XM_011526844.2:c.916_918del	XP_011525146.1:p.Glu306del
XM_017026665.1:c.3169_3171del	XP_016882154.1:p.Glu1057del
NM_001083961.2:c.3169_3171del MANE Select	NP_001077430.1:p.Glu1057del
NM_173636.5:c.3169_3171del	NP_775907.4:p.Glu1057del