Canonical Allele Identifier: CA307842011

Gene: WDR62

Linked Data

• ClinVar Variation Id: 2446668
• ClinVar RCV Id: RCV003159498
• dbSNP Id: rs776996104
• gnomAD v3: 19-36102023-G-A
• gnomAD v4: 19-36102023-G-A
• MyVariant Identifiers: chr19:g.36592925G>A (hg19) ; chr19:g.36102023G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102023G>A , CM000681.2:g.36102023G>A	GRCh38
NC_000019.9:g.36592925G>A , CM000681.1:g.36592925G>A	GRCh37
NC_000019.8:g.41284765G>A	NCBI36
NG_028101.1:g.52143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3092G>A	ENSP00000270301.6:p.Gly1031Asp
ENST00000401500.7:c.3092G>A MANE Select	ENSP00000384792.1:p.Gly1031Asp
ENST00000587391.6:c.*2367G>A	ENSP00000465525.1:n.*2367G>A
ENST00000679357.1:c.882G>A
ENST00000679422.1:c.771G>A
ENST00000679682.1:c.3077G>A	ENSP00000506226.1:p.Gly1026Asp
ENST00000679714.1:c.3086G>A	ENSP00000506627.1:p.Gly1029Asp
ENST00000679757.1:c.2741G>A	ENSP00000505158.1:p.Gly914Asp
ENST00000679858.1:c.*2474G>A	ENSP00000505655.1:n.*2474G>A
ENST00000680211.1:c.-308G>A	ENSP00000506102.1:n.-308G>A
ENST00000680349.1:n.1075G>A
ENST00000680403.1:c.3092G>A	ENSP00000505677.1:p.Gly1031Asp
ENST00000680564.1:c.2971+706G>A	ENSP00000505582.1:n.2971+706G>A
ENST00000680590.1:c.*1487G>A	ENSP00000505350.1:n.*1487G>A
ENST00000680739.1:c.10G>A
ENST00000680773.1:n.1008G>A
ENST00000680806.1:c.*1810G>A	ENSP00000506418.1:n.*1810G>A
ENST00000680997.1:n.439G>A
ENST00000681088.1:c.754G>A
ENST00000681608.1:n.40G>A
ENST00000681625.1:c.*424G>A	ENSP00000505555.1:n.*424G>A
ENST00000270301.11:c.3092G>A	ENSP00000270301.6:p.Gly1031Asp
ENST00000401500.6:c.3092G>A	ENSP00000384792.1:p.Gly1031Asp
ENST00000587391.5:c.*2367G>A	ENSP00000465525.1:n.*2367G>A
NM_001083961.1:c.3092G>A	NP_001077430.1:p.Gly1031Asp
NM_173636.4:c.3092G>A	NP_775907.4:p.Gly1031Asp
XM_005258809.2:c.2981G>A	XP_005258866.1:p.Gly994Asp
XM_011526837.1:c.3077G>A	XP_011525139.1:p.Gly1026Asp
XM_011526838.1:c.2971+706G>A	XP_011525140.1:n.2971+706G>A
XM_011526839.1:c.2741G>A	XP_011525141.1:p.Gly914Asp
XM_011526840.1:c.2084G>A	XP_011525142.1:p.Gly695Asp
XM_011526841.1:c.1670G>A	XP_011525143.1:p.Gly557Asp
XM_011526842.1:c.1523G>A	XP_011525144.1:p.Gly508Asp
XM_011526843.1:c.839G>A	XP_011525145.1:p.Gly280Asp
XM_011526844.1:c.839G>A	XP_011525146.1:p.Gly280Asp
XM_011526840.2:c.2084G>A	XP_011525142.1:p.Gly695Asp
XM_011526841.2:c.1670G>A	XP_011525143.1:p.Gly557Asp
XM_011526844.2:c.839G>A	XP_011525146.1:p.Gly280Asp
XM_017026665.1:c.3092G>A	XP_016882154.1:p.Gly1031Asp
NM_001083961.2:c.3092G>A MANE Select	NP_001077430.1:p.Gly1031Asp
NM_173636.5:c.3092G>A	NP_775907.4:p.Gly1031Asp