Canonical Allele Identifier: CA2576761940

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102060del , CM000681.2:g.36102060del	GRCh38
NC_000019.9:g.36592962del , CM000681.1:g.36592962del	GRCh37
NC_000019.8:g.41284802del	NCBI36
NG_028101.1:g.52180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3129del	ENSP00000270301.6:p.Ser1044AlafsTer24
ENST00000401500.7:c.3129del MANE Select	ENSP00000384792.1:p.Ser1044AlafsTer24
ENST00000587391.6:c.*2404del	ENSP00000465525.1:n.*2404del
ENST00000679357.1:c.919del
ENST00000679422.1:c.808del
ENST00000679682.1:c.3114del	ENSP00000506226.1:p.Ser1039AlafsTer24
ENST00000679714.1:c.3123del	ENSP00000506627.1:p.Ser1042AlafsTer24
ENST00000679757.1:c.2778del	ENSP00000505158.1:p.Ser927AlafsTer24
ENST00000679858.1:c.*2511del	ENSP00000505655.1:n.*2511del
ENST00000680211.1:c.-271del	ENSP00000506102.1:n.-271del
ENST00000680349.1:n.1112del
ENST00000680403.1:c.3129del	ENSP00000505677.1:p.Ser1044AlafsTer24
ENST00000680564.1:c.2972-677del	ENSP00000505582.1:n.2972-677del
ENST00000680590.1:c.*1524del	ENSP00000505350.1:n.*1524del
ENST00000680739.1:c.47del
ENST00000680773.1:n.1045del
ENST00000680806.1:c.*1847del	ENSP00000506418.1:n.*1847del
ENST00000680997.1:n.476del
ENST00000681088.1:c.791del
ENST00000681608.1:n.77del
ENST00000681625.1:c.*461del	ENSP00000505555.1:n.*461del
ENST00000270301.11:c.3129del	ENSP00000270301.6:p.Ser1044AlafsTer24
ENST00000401500.6:c.3129del	ENSP00000384792.1:p.Ser1044AlafsTer24
ENST00000587391.5:c.*2404del	ENSP00000465525.1:n.*2404del
NM_001083961.1:c.3129del	NP_001077430.1:p.Ser1044AlafsTer24
NM_173636.4:c.3129del	NP_775907.4:p.Ser1044AlafsTer24
XM_005258809.2:c.3018del	XP_005258866.1:p.Ser1007AlafsTer24
XM_011526837.1:c.3114del	XP_011525139.1:p.Ser1039AlafsTer24
XM_011526838.1:c.2972-677del	XP_011525140.1:n.2972-677del
XM_011526839.1:c.2778del	XP_011525141.1:p.Ser927AlafsTer24
XM_011526840.1:c.2121del	XP_011525142.1:p.Ser708AlafsTer24
XM_011526841.1:c.1707del	XP_011525143.1:p.Ser570AlafsTer24
XM_011526842.1:c.1560del	XP_011525144.1:p.Ser521AlafsTer24
XM_011526843.1:c.876del	XP_011525145.1:p.Ser293AlafsTer24
XM_011526844.1:c.876del	XP_011525146.1:p.Ser293AlafsTer24
XM_011526840.2:c.2121del	XP_011525142.1:p.Ser708AlafsTer24
XM_011526841.2:c.1707del	XP_011525143.1:p.Ser570AlafsTer24
XM_011526844.2:c.876del	XP_011525146.1:p.Ser293AlafsTer24
XM_017026665.1:c.3129del	XP_016882154.1:p.Ser1044AlafsTer24
NM_001083961.2:c.3129del MANE Select	NP_001077430.1:p.Ser1044AlafsTer24
NM_173636.5:c.3129del	NP_775907.4:p.Ser1044AlafsTer24