Canonical Allele Identifier: CA632783704

Gene: WDR62

Linked Data

• dbSNP Id: rs1466288586
• gnomAD v2: 19-36583570-GTC-G
• gnomAD v3: 19-36092668-GTC-G
• gnomAD v4: 19-36092668-GTC-G
• MyVariant Identifiers: chr19:g.36583571_36583572del (hg19) ; chr19:g.36092669_36092670del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36092674_36092675del , CM000681.2:g.36092674_36092675del	GRCh38
NC_000019.9:g.36583576_36583577del , CM000681.1:g.36583576_36583577del	GRCh37
NC_000019.8:g.41275416_41275417del	NCBI36
NG_028101.1:g.42794_42795del

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.2211-15_2211-14del	ENSP00000270301.6:n.2211-15_2211-14del
ENST00000401500.7:c.2211-15_2211-14del MANE Select	ENSP00000384792.1:n.2211-15_2211-14del
ENST00000587391.6:c.*901-15_*901-14del	ENSP00000465525.1:n.*901-15_*901-14del
ENST00000679682.1:c.2196-15_2196-14del	ENSP00000506226.1:n.2196-15_2196-14del
ENST00000679714.1:c.2205-15_2205-14del	ENSP00000506627.1:n.2205-15_2205-14del
ENST00000679757.1:c.1860-15_1860-14del	ENSP00000505158.1:n.1860-15_1860-14del
ENST00000679858.1:c.*1008-15_*1008-14del	ENSP00000505655.1:n.*1008-15_*1008-14del
ENST00000680349.1:n.194-15_194-14del
ENST00000680377.1:c.485-15_485-14del
ENST00000680403.1:c.2211-15_2211-14del	ENSP00000505677.1:n.2211-15_2211-14del
ENST00000680489.1:n.2534-15_2534-14del
ENST00000680564.1:c.2211-15_2211-14del	ENSP00000505582.1:n.2211-15_2211-14del
ENST00000680590.1:c.*610-15_*610-14del	ENSP00000505350.1:n.*610-15_*610-14del
ENST00000680806.1:c.*1040-15_*1040-14del	ENSP00000506418.1:n.*1040-15_*1040-14del
ENST00000680858.1:c.409-15_409-14del
ENST00000681302.1:c.597-15_597-14del
ENST00000681625.1:c.2196-15_2196-14del	ENSP00000505555.1:n.2196-15_2196-14del
ENST00000270301.11:c.2211-15_2211-14del	ENSP00000270301.6:n.2211-15_2211-14del
ENST00000401500.6:c.2211-15_2211-14del	ENSP00000384792.1:n.2211-15_2211-14del
ENST00000587391.5:c.*901-15_*901-14del	ENSP00000465525.1:n.*901-15_*901-14del
NM_001083961.1:c.2211-15_2211-14del	NP_001077430.1:n.2211-15_2211-14del
NM_173636.4:c.2211-15_2211-14del	NP_775907.4:n.2211-15_2211-14del
XM_005258809.2:c.2211-15_2211-14del	XP_005258866.1:n.2211-15_2211-14del
XM_011526837.1:c.2196-15_2196-14del	XP_011525139.1:n.2196-15_2196-14del
XM_011526838.1:c.2211-15_2211-14del	XP_011525140.1:n.2211-15_2211-14del
XM_011526839.1:c.1860-15_1860-14del	XP_011525141.1:n.1860-15_1860-14del
XM_011526840.1:c.1203-15_1203-14del	XP_011525142.1:n.1203-15_1203-14del
XM_011526841.1:c.789-15_789-14del	XP_011525143.1:n.789-15_789-14del
XM_011526842.1:c.642-15_642-14del	XP_011525144.1:n.642-15_642-14del
XM_011526843.1:c.-43-15_-43-14del	XP_011525145.1:n.-43-15_-43-14del
XM_011526844.1:c.-43-15_-43-14del	XP_011525146.1:n.-43-15_-43-14del
XM_011526840.2:c.1203-15_1203-14del	XP_011525142.1:n.1203-15_1203-14del
XM_011526841.2:c.789-15_789-14del	XP_011525143.1:n.789-15_789-14del
XM_011526844.2:c.-43-15_-43-14del	XP_011525146.1:n.-43-15_-43-14del
XM_017026665.1:c.2211-15_2211-14del	XP_016882154.1:n.2211-15_2211-14del
XR_001753671.1:n.2238-15_2238-14del
XR_001753672.1:n.2126-15_2126-14del
NM_001083961.2:c.2211-15_2211-14del MANE Select	NP_001077430.1:n.2211-15_2211-14del
NM_173636.5:c.2211-15_2211-14del	NP_775907.4:n.2211-15_2211-14del