Canonical Allele Identifier: CA2333972058

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104256_36104258delinsGAC , CM000681.2:g.36104256_36104258delinsGAC	GRCh38
NC_000019.9:g.36595158_36595160delinsGAC , CM000681.1:g.36595158_36595160delinsGAC	GRCh37
NC_000019.8:g.41286998_41287000delinsGAC	NCBI36
NG_028101.1:g.54376_54378delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4139-262_4139-260delinsGAC	ENSP00000270301.6:n.4139-262_4139-260delinsGAC
ENST00000401500.7:c.4154-262_4154-260delinsGAC MANE Select	ENSP00000384792.1:n.4154-262_4154-260delinsGAC
ENST00000587391.6:c.*4014-262_*4014-260delinsGAC	ENSP00000465525.1:n.*4014-262_*4014-260delinsGAC
ENST00000679357.1:c.2234-262_2234-260delinsGAC
ENST00000679598.1:c.918+275_918+277delinsGAC
ENST00000679682.1:c.4139-262_4139-260delinsGAC	ENSP00000506226.1:n.4139-262_4139-260delinsGAC
ENST00000679714.1:c.4148-262_4148-260delinsGAC	ENSP00000506627.1:n.4148-262_4148-260delinsGAC
ENST00000679757.1:c.3803-262_3803-260delinsGAC	ENSP00000505158.1:n.3803-262_3803-260delinsGAC
ENST00000679858.1:c.*3536-262_*3536-260delinsGAC	ENSP00000505655.1:n.*3536-262_*3536-260delinsGAC
ENST00000680211.1:c.755-262_755-260delinsGAC	ENSP00000506102.1:n.755-262_755-260delinsGAC
ENST00000680280.1:n.1657-262_1657-260delinsGAC
ENST00000680349.1:n.2803-262_2803-260delinsGAC
ENST00000680403.1:c.4139-262_4139-260delinsGAC	ENSP00000505677.1:n.4139-262_4139-260delinsGAC
ENST00000680564.1:c.3905-262_3905-260delinsGAC	ENSP00000505582.1:n.3905-262_3905-260delinsGAC
ENST00000680590.1:c.*2534-262_*2534-260delinsGAC	ENSP00000505350.1:n.*2534-262_*2534-260delinsGAC
ENST00000680597.1:c.887-262_887-260delinsGAC
ENST00000680739.1:c.1169-262_1169-260delinsGAC
ENST00000680773.1:n.2655-262_2655-260delinsGAC
ENST00000680806.1:c.*3457-262_*3457-260delinsGAC	ENSP00000506418.1:n.*3457-262_*3457-260delinsGAC
ENST00000680997.1:n.2086-262_2086-260delinsGAC
ENST00000681608.1:n.1999-262_1999-260delinsGAC
ENST00000681625.1:c.*1486-262_*1486-260delinsGAC	ENSP00000505555.1:n.*1486-262_*1486-260delinsGAC
ENST00000681648.1:n.1943_1945delinsGAC
ENST00000270301.11:c.4139-262_4139-260delinsGAC	ENSP00000270301.6:n.4139-262_4139-260delinsGAC
ENST00000401500.6:c.4154-262_4154-260delinsGAC	ENSP00000384792.1:n.4154-262_4154-260delinsGAC
ENST00000587391.5:c.*4014-262_*4014-260delinsGAC	ENSP00000465525.1:n.*4014-262_*4014-260delinsGAC
NM_001083961.1:c.4154-262_4154-260delinsGAC	NP_001077430.1:n.4154-262_4154-260delinsGAC
NM_173636.4:c.4139-262_4139-260delinsGAC	NP_775907.4:n.4139-262_4139-260delinsGAC
XM_005258809.2:c.4043-262_4043-260delinsGAC	XP_005258866.1:n.4043-262_4043-260delinsGAC
XM_011526837.1:c.4139-262_4139-260delinsGAC	XP_011525139.1:n.4139-262_4139-260delinsGAC
XM_011526838.1:c.3905-262_3905-260delinsGAC	XP_011525140.1:n.3905-262_3905-260delinsGAC
XM_011526839.1:c.3803-262_3803-260delinsGAC	XP_011525141.1:n.3803-262_3803-260delinsGAC
XM_011526840.1:c.3146-262_3146-260delinsGAC	XP_011525142.1:n.3146-262_3146-260delinsGAC
XM_011526841.1:c.2732-262_2732-260delinsGAC	XP_011525143.1:n.2732-262_2732-260delinsGAC
XM_011526842.1:c.2585-262_2585-260delinsGAC	XP_011525144.1:n.2585-262_2585-260delinsGAC
XM_011526843.1:c.1901-262_1901-260delinsGAC	XP_011525145.1:n.1901-262_1901-260delinsGAC
XM_011526844.1:c.1901-262_1901-260delinsGAC	XP_011525146.1:n.1901-262_1901-260delinsGAC
XM_011526840.2:c.3146-262_3146-260delinsGAC	XP_011525142.1:n.3146-262_3146-260delinsGAC
XM_011526841.2:c.2732-262_2732-260delinsGAC	XP_011525143.1:n.2732-262_2732-260delinsGAC
XM_011526844.2:c.1901-262_1901-260delinsGAC	XP_011525146.1:n.1901-262_1901-260delinsGAC
XM_017026665.1:c.4154-262_4154-260delinsGAC	XP_016882154.1:n.4154-262_4154-260delinsGAC
NM_001083961.2:c.4154-262_4154-260delinsGAC MANE Select	NP_001077430.1:n.4154-262_4154-260delinsGAC
NM_173636.5:c.4139-262_4139-260delinsGAC	NP_775907.4:n.4139-262_4139-260delinsGAC