Canonical Allele Identifier: CA2584644424

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101973-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101975del , CM000681.2:g.36101975del	GRCh38
NC_000019.9:g.36592877del , CM000681.1:g.36592877del	GRCh37
NC_000019.8:g.41284717del	NCBI36
NG_028101.1:g.52095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3083-39del	ENSP00000270301.6:n.3083-39del
ENST00000401500.7:c.3083-39del MANE Select	ENSP00000384792.1:n.3083-39del
ENST00000587391.6:c.*2319del	ENSP00000465525.1:n.*2319del
ENST00000679357.1:c.873-39del
ENST00000679422.1:c.762-39del
ENST00000679682.1:c.3068-39del	ENSP00000506226.1:n.3068-39del
ENST00000679714.1:c.3077-39del	ENSP00000506627.1:n.3077-39del
ENST00000679757.1:c.2732-39del	ENSP00000505158.1:n.2732-39del
ENST00000679858.1:c.*2426del	ENSP00000505655.1:n.*2426del
ENST00000680211.1:c.-317-39del	ENSP00000506102.1:n.-317-39del
ENST00000680349.1:n.1066-39del
ENST00000680403.1:c.3083-39del	ENSP00000505677.1:n.3083-39del
ENST00000680564.1:c.2971+658del	ENSP00000505582.1:n.2971+658del
ENST00000680590.1:c.*1478-39del	ENSP00000505350.1:n.*1478-39del
ENST00000680773.1:n.960del
ENST00000680806.1:c.*1801-39del	ENSP00000506418.1:n.*1801-39del
ENST00000680997.1:n.430-39del
ENST00000681088.1:c.745-39del
ENST00000681608.1:n.31-39del
ENST00000681625.1:c.*415-39del	ENSP00000505555.1:n.*415-39del
ENST00000270301.11:c.3083-39del	ENSP00000270301.6:n.3083-39del
ENST00000401500.6:c.3083-39del	ENSP00000384792.1:n.3083-39del
ENST00000587391.5:c.*2319del	ENSP00000465525.1:n.*2319del
NM_001083961.1:c.3083-39del	NP_001077430.1:n.3083-39del
NM_173636.4:c.3083-39del	NP_775907.4:n.3083-39del
XM_005258809.2:c.2972-39del	XP_005258866.1:n.2972-39del
XM_011526837.1:c.3068-39del	XP_011525139.1:n.3068-39del
XM_011526838.1:c.2971+658del	XP_011525140.1:n.2971+658del
XM_011526839.1:c.2732-39del	XP_011525141.1:n.2732-39del
XM_011526840.1:c.2075-39del	XP_011525142.1:n.2075-39del
XM_011526841.1:c.1661-39del	XP_011525143.1:n.1661-39del
XM_011526842.1:c.1514-39del	XP_011525144.1:n.1514-39del
XM_011526843.1:c.830-39del	XP_011525145.1:n.830-39del
XM_011526844.1:c.830-39del	XP_011525146.1:n.830-39del
XM_011526840.2:c.2075-39del	XP_011525142.1:n.2075-39del
XM_011526841.2:c.1661-39del	XP_011525143.1:n.1661-39del
XM_011526844.2:c.830-39del	XP_011525146.1:n.830-39del
XM_017026665.1:c.3083-39del	XP_016882154.1:n.3083-39del
NM_001083961.2:c.3083-39del MANE Select	NP_001077430.1:n.3083-39del
NM_173636.5:c.3083-39del	NP_775907.4:n.3083-39del