Canonical Allele Identifier: CA881851574

Gene: WDR62

Linked Data

• dbSNP Id: rs1461777518
• gnomAD v4: 19-36102128-CACTG-C
• MyVariant Identifiers: chr19:g.36593031_36593034del (hg19) ; chr19:g.36102129_36102132del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102134_36102137del , CM000681.2:g.36102134_36102137del	GRCh38
NC_000019.9:g.36593036_36593039del , CM000681.1:g.36593036_36593039del	GRCh37
NC_000019.8:g.41284876_41284879del	NCBI36
NG_028101.1:g.52254_52257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3203_3206del	ENSP00000270301.6:p.Thr1068SerfsTer24
ENST00000401500.7:c.3203_3206del MANE Select	ENSP00000384792.1:p.Thr1068SerfsTer29
ENST00000587391.6:c.*2478_*2481del	ENSP00000465525.1:n.*2478_*2481del
ENST00000679357.1:c.993_996del
ENST00000679422.1:c.882_885del
ENST00000679682.1:c.3188_3191del	ENSP00000506226.1:p.Thr1063SerfsTer29
ENST00000679714.1:c.3197_3200del	ENSP00000506627.1:p.Thr1066SerfsTer29
ENST00000679757.1:c.2852_2855del	ENSP00000505158.1:p.Thr951SerfsTer29
ENST00000679858.1:c.*2585_*2588del	ENSP00000505655.1:n.*2585_*2588del
ENST00000680211.1:c.-197_-194del	ENSP00000506102.1:n.-197_-194del
ENST00000680349.1:n.1186_1189del
ENST00000680403.1:c.3203_3206del	ENSP00000505677.1:p.Thr1068SerfsTer24
ENST00000680564.1:c.2972-603_2972-600del	ENSP00000505582.1:n.2972-603_2972-600del
ENST00000680590.1:c.*1598_*1601del	ENSP00000505350.1:n.*1598_*1601del
ENST00000680739.1:c.121_124del
ENST00000680773.1:n.1119_1122del
ENST00000680806.1:c.*1921_*1924del	ENSP00000506418.1:n.*1921_*1924del
ENST00000680997.1:n.550_553del
ENST00000681088.1:c.865_868del
ENST00000681608.1:n.151_154del
ENST00000681625.1:c.*535_*538del	ENSP00000505555.1:n.*535_*538del
ENST00000270301.11:c.3203_3206del	ENSP00000270301.6:p.Thr1068SerfsTer24
ENST00000401500.6:c.3203_3206del	ENSP00000384792.1:p.Thr1068SerfsTer29
ENST00000587391.5:c.*2478_*2481del	ENSP00000465525.1:n.*2478_*2481del
NM_001083961.1:c.3203_3206del	NP_001077430.1:p.Thr1068SerfsTer29
NM_173636.4:c.3203_3206del	NP_775907.4:p.Thr1068SerfsTer24
XM_005258809.2:c.3092_3095del	XP_005258866.1:p.Thr1031SerfsTer29
XM_011526837.1:c.3188_3191del	XP_011525139.1:p.Thr1063SerfsTer29
XM_011526838.1:c.2972-603_2972-600del	XP_011525140.1:n.2972-603_2972-600del
XM_011526839.1:c.2852_2855del	XP_011525141.1:p.Thr951SerfsTer29
XM_011526840.1:c.2195_2198del	XP_011525142.1:p.Thr732SerfsTer29
XM_011526841.1:c.1781_1784del	XP_011525143.1:p.Thr594SerfsTer29
XM_011526842.1:c.1634_1637del	XP_011525144.1:p.Thr545SerfsTer29
XM_011526843.1:c.950_953del	XP_011525145.1:p.Thr317SerfsTer29
XM_011526844.1:c.950_953del	XP_011525146.1:p.Thr317SerfsTer29
XM_011526840.2:c.2195_2198del	XP_011525142.1:p.Thr732SerfsTer29
XM_011526841.2:c.1781_1784del	XP_011525143.1:p.Thr594SerfsTer29
XM_011526844.2:c.950_953del	XP_011525146.1:p.Thr317SerfsTer29
XM_017026665.1:c.3203_3206del	XP_016882154.1:p.Thr1068SerfsTer29
NM_001083961.2:c.3203_3206del MANE Select	NP_001077430.1:p.Thr1068SerfsTer29
NM_173636.5:c.3203_3206del	NP_775907.4:p.Thr1068SerfsTer24