Canonical Allele Identifier: CA307842922

Gene: WDR62

Linked Data

• dbSNP Id: rs963236760
• gnomAD v2: 19-36595235-TAAG-T
• gnomAD v3: 19-36104333-TAAG-T
• gnomAD v4: 19-36104333-TAAG-T
• MyVariant Identifiers: chr19:g.36595236_36595238del (hg19) ; chr19:g.36104334_36104336del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104338_36104340del , CM000681.2:g.36104338_36104340del	GRCh38
NC_000019.9:g.36595240_36595242del , CM000681.1:g.36595240_36595242del	GRCh37
NC_000019.8:g.41287080_41287082del	NCBI36
NG_028101.1:g.54458_54460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4139-180_4139-178del	ENSP00000270301.6:n.4139-180_4139-178del
ENST00000401500.7:c.4154-180_4154-178del MANE Select	ENSP00000384792.1:n.4154-180_4154-178del
ENST00000587391.6:c.*4014-180_*4014-178del	ENSP00000465525.1:n.*4014-180_*4014-178del
ENST00000679357.1:c.2234-180_2234-178del
ENST00000679598.1:c.919-200_919-198del
ENST00000679682.1:c.4139-180_4139-178del	ENSP00000506226.1:n.4139-180_4139-178del
ENST00000679714.1:c.4148-180_4148-178del	ENSP00000506627.1:n.4148-180_4148-178del
ENST00000679757.1:c.3803-180_3803-178del	ENSP00000505158.1:n.3803-180_3803-178del
ENST00000679858.1:c.*3536-180_*3536-178del	ENSP00000505655.1:n.*3536-180_*3536-178del
ENST00000680211.1:c.755-180_755-178del	ENSP00000506102.1:n.755-180_755-178del
ENST00000680280.1:n.1657-180_1657-178del
ENST00000680349.1:n.2803-180_2803-178del
ENST00000680403.1:c.4139-180_4139-178del	ENSP00000505677.1:n.4139-180_4139-178del
ENST00000680564.1:c.3905-180_3905-178del	ENSP00000505582.1:n.3905-180_3905-178del
ENST00000680590.1:c.*2534-180_*2534-178del	ENSP00000505350.1:n.*2534-180_*2534-178del
ENST00000680597.1:c.887-180_887-178del
ENST00000680739.1:c.1169-180_1169-178del
ENST00000680773.1:n.2655-180_2655-178del
ENST00000680806.1:c.*3457-180_*3457-178del	ENSP00000506418.1:n.*3457-180_*3457-178del
ENST00000680997.1:n.2086-180_2086-178del
ENST00000681608.1:n.1999-180_1999-178del
ENST00000681625.1:c.*1486-180_*1486-178del	ENSP00000505555.1:n.*1486-180_*1486-178del
ENST00000681648.1:n.2025_2027del
ENST00000270301.11:c.4139-180_4139-178del	ENSP00000270301.6:n.4139-180_4139-178del
ENST00000401500.6:c.4154-180_4154-178del	ENSP00000384792.1:n.4154-180_4154-178del
ENST00000587391.5:c.*4014-180_*4014-178del	ENSP00000465525.1:n.*4014-180_*4014-178del
NM_001083961.1:c.4154-180_4154-178del	NP_001077430.1:n.4154-180_4154-178del
NM_173636.4:c.4139-180_4139-178del	NP_775907.4:n.4139-180_4139-178del
XM_005258809.2:c.4043-180_4043-178del	XP_005258866.1:n.4043-180_4043-178del
XM_011526837.1:c.4139-180_4139-178del	XP_011525139.1:n.4139-180_4139-178del
XM_011526838.1:c.3905-180_3905-178del	XP_011525140.1:n.3905-180_3905-178del
XM_011526839.1:c.3803-180_3803-178del	XP_011525141.1:n.3803-180_3803-178del
XM_011526840.1:c.3146-180_3146-178del	XP_011525142.1:n.3146-180_3146-178del
XM_011526841.1:c.2732-180_2732-178del	XP_011525143.1:n.2732-180_2732-178del
XM_011526842.1:c.2585-180_2585-178del	XP_011525144.1:n.2585-180_2585-178del
XM_011526843.1:c.1901-180_1901-178del	XP_011525145.1:n.1901-180_1901-178del
XM_011526844.1:c.1901-180_1901-178del	XP_011525146.1:n.1901-180_1901-178del
XM_011526840.2:c.3146-180_3146-178del	XP_011525142.1:n.3146-180_3146-178del
XM_011526841.2:c.2732-180_2732-178del	XP_011525143.1:n.2732-180_2732-178del
XM_011526844.2:c.1901-180_1901-178del	XP_011525146.1:n.1901-180_1901-178del
XM_017026665.1:c.4154-180_4154-178del	XP_016882154.1:n.4154-180_4154-178del
NM_001083961.2:c.4154-180_4154-178del MANE Select	NP_001077430.1:n.4154-180_4154-178del
NM_173636.5:c.4139-180_4139-178del	NP_775907.4:n.4139-180_4139-178del