Canonical Allele Identifier: CA632787946

Gene: WDR62

Linked Data

• dbSNP Id: rs1157284072
• gnomAD v2: 19-36595280-TAGGAGTGAAGGGGAGGG-T
• gnomAD v3: 19-36104378-TAGGAGTGAAGGGGAGGG-T
• gnomAD v4: 19-36104378-TAGGAGTGAAGGGGAGGG-T
• MyVariant Identifiers: chr19:g.36595281_36595297del (hg19) ; chr19:g.36104379_36104395del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104381_36104397del , CM000681.2:g.36104381_36104397del	GRCh38
NC_000019.9:g.36595283_36595299del , CM000681.1:g.36595283_36595299del	GRCh37
NC_000019.8:g.41287123_41287139del	NCBI36
NG_028101.1:g.54501_54517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4139-137_4139-121del	ENSP00000270301.6:n.4139-137_4139-121del
ENST00000401500.7:c.4154-137_4154-121del MANE Select	ENSP00000384792.1:n.4154-137_4154-121del
ENST00000587391.6:c.*4014-137_*4014-121del	ENSP00000465525.1:n.*4014-137_*4014-121del
ENST00000679357.1:c.2234-137_2234-121del
ENST00000679598.1:c.919-157_919-141del
ENST00000679682.1:c.4139-137_4139-121del	ENSP00000506226.1:n.4139-137_4139-121del
ENST00000679714.1:c.4148-137_4148-121del	ENSP00000506627.1:n.4148-137_4148-121del
ENST00000679757.1:c.3803-137_3803-121del	ENSP00000505158.1:n.3803-137_3803-121del
ENST00000679858.1:c.*3536-137_*3536-121del	ENSP00000505655.1:n.*3536-137_*3536-121del
ENST00000680211.1:c.755-137_755-121del	ENSP00000506102.1:n.755-137_755-121del
ENST00000680280.1:n.1657-137_1657-121del
ENST00000680349.1:n.2803-137_2803-121del
ENST00000680403.1:c.4139-137_4139-121del	ENSP00000505677.1:n.4139-137_4139-121del
ENST00000680564.1:c.3905-137_3905-121del	ENSP00000505582.1:n.3905-137_3905-121del
ENST00000680590.1:c.*2534-137_*2534-121del	ENSP00000505350.1:n.*2534-137_*2534-121del
ENST00000680597.1:c.887-137_887-121del
ENST00000680739.1:c.1169-137_1169-121del
ENST00000680773.1:n.2655-137_2655-121del
ENST00000680806.1:c.*3457-137_*3457-121del	ENSP00000506418.1:n.*3457-137_*3457-121del
ENST00000680997.1:n.2086-137_2086-121del
ENST00000681608.1:n.1999-137_1999-121del
ENST00000681625.1:c.*1486-137_*1486-121del	ENSP00000505555.1:n.*1486-137_*1486-121del
ENST00000681648.1:n.2068_2084del
ENST00000270301.11:c.4139-137_4139-121del	ENSP00000270301.6:n.4139-137_4139-121del
ENST00000401500.6:c.4154-137_4154-121del	ENSP00000384792.1:n.4154-137_4154-121del
ENST00000587391.5:c.*4014-137_*4014-121del	ENSP00000465525.1:n.*4014-137_*4014-121del
NM_001083961.1:c.4154-137_4154-121del	NP_001077430.1:n.4154-137_4154-121del
NM_173636.4:c.4139-137_4139-121del	NP_775907.4:n.4139-137_4139-121del
XM_005258809.2:c.4043-137_4043-121del	XP_005258866.1:n.4043-137_4043-121del
XM_011526837.1:c.4139-137_4139-121del	XP_011525139.1:n.4139-137_4139-121del
XM_011526838.1:c.3905-137_3905-121del	XP_011525140.1:n.3905-137_3905-121del
XM_011526839.1:c.3803-137_3803-121del	XP_011525141.1:n.3803-137_3803-121del
XM_011526840.1:c.3146-137_3146-121del	XP_011525142.1:n.3146-137_3146-121del
XM_011526841.1:c.2732-137_2732-121del	XP_011525143.1:n.2732-137_2732-121del
XM_011526842.1:c.2585-137_2585-121del	XP_011525144.1:n.2585-137_2585-121del
XM_011526843.1:c.1901-137_1901-121del	XP_011525145.1:n.1901-137_1901-121del
XM_011526844.1:c.1901-137_1901-121del	XP_011525146.1:n.1901-137_1901-121del
XM_011526840.2:c.3146-137_3146-121del	XP_011525142.1:n.3146-137_3146-121del
XM_011526841.2:c.2732-137_2732-121del	XP_011525143.1:n.2732-137_2732-121del
XM_011526844.2:c.1901-137_1901-121del	XP_011525146.1:n.1901-137_1901-121del
XM_017026665.1:c.4154-137_4154-121del	XP_016882154.1:n.4154-137_4154-121del
NM_001083961.2:c.4154-137_4154-121del MANE Select	NP_001077430.1:n.4154-137_4154-121del
NM_173636.5:c.4139-137_4139-121del	NP_775907.4:n.4139-137_4139-121del