Canonical Allele Identifier: CA632787320

Gene: WDR62

Linked Data

• dbSNP Id: rs1348735298
• gnomAD v2: 19-36592931-CAGA-C
• gnomAD v4: 19-36102029-CAGA-C
• MyVariant Identifiers: chr19:g.36592932_36592934del (hg19) ; chr19:g.36102030_36102032del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102033_36102035del , CM000681.2:g.36102033_36102035del	GRCh38
NC_000019.9:g.36592935_36592937del , CM000681.1:g.36592935_36592937del	GRCh37
NC_000019.8:g.41284775_41284777del	NCBI36
NG_028101.1:g.52153_52155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3102_3104del	ENSP00000270301.6:p.Glu1034del
ENST00000401500.7:c.3102_3104del MANE Select	ENSP00000384792.1:p.Glu1034del
ENST00000587391.6:c.*2377_*2379del	ENSP00000465525.1:n.*2377_*2379del
ENST00000679357.1:c.892_894del
ENST00000679422.1:c.781_783del
ENST00000679682.1:c.3087_3089del	ENSP00000506226.1:p.Glu1029del
ENST00000679714.1:c.3096_3098del	ENSP00000506627.1:p.Glu1032del
ENST00000679757.1:c.2751_2753del	ENSP00000505158.1:p.Glu917del
ENST00000679858.1:c.*2484_*2486del	ENSP00000505655.1:n.*2484_*2486del
ENST00000680211.1:c.-298_-296del	ENSP00000506102.1:n.-298_-296del
ENST00000680349.1:n.1085_1087del
ENST00000680403.1:c.3102_3104del	ENSP00000505677.1:p.Glu1034del
ENST00000680564.1:c.2972-704_2972-702del	ENSP00000505582.1:n.2972-704_2972-702del
ENST00000680590.1:c.*1497_*1499del	ENSP00000505350.1:n.*1497_*1499del
ENST00000680739.1:c.20_22del
ENST00000680773.1:n.1018_1020del
ENST00000680806.1:c.*1820_*1822del	ENSP00000506418.1:n.*1820_*1822del
ENST00000680997.1:n.449_451del
ENST00000681088.1:c.764_766del
ENST00000681608.1:n.50_52del
ENST00000681625.1:c.*434_*436del	ENSP00000505555.1:n.*434_*436del
ENST00000270301.11:c.3102_3104del	ENSP00000270301.6:p.Glu1034del
ENST00000401500.6:c.3102_3104del	ENSP00000384792.1:p.Glu1034del
ENST00000587391.5:c.*2377_*2379del	ENSP00000465525.1:n.*2377_*2379del
NM_001083961.1:c.3102_3104del	NP_001077430.1:p.Glu1034del
NM_173636.4:c.3102_3104del	NP_775907.4:p.Glu1034del
XM_005258809.2:c.2991_2993del	XP_005258866.1:p.Glu997del
XM_011526837.1:c.3087_3089del	XP_011525139.1:p.Glu1029del
XM_011526838.1:c.2972-704_2972-702del	XP_011525140.1:n.2972-704_2972-702del
XM_011526839.1:c.2751_2753del	XP_011525141.1:p.Glu917del
XM_011526840.1:c.2094_2096del	XP_011525142.1:p.Glu698del
XM_011526841.1:c.1680_1682del	XP_011525143.1:p.Glu560del
XM_011526842.1:c.1533_1535del	XP_011525144.1:p.Glu511del
XM_011526843.1:c.849_851del	XP_011525145.1:p.Glu283del
XM_011526844.1:c.849_851del	XP_011525146.1:p.Glu283del
XM_011526840.2:c.2094_2096del	XP_011525142.1:p.Glu698del
XM_011526841.2:c.1680_1682del	XP_011525143.1:p.Glu560del
XM_011526844.2:c.849_851del	XP_011525146.1:p.Glu283del
XM_017026665.1:c.3102_3104del	XP_016882154.1:p.Glu1034del
NM_001083961.2:c.3102_3104del MANE Select	NP_001077430.1:p.Glu1034del
NM_173636.5:c.3102_3104del	NP_775907.4:p.Glu1034del