Canonical Allele Identifier: CA405449460

Gene: WDR62

Linked Data

• dbSNP Id: rs1437696352
• gnomAD v2: 19-36592640-G-A
• gnomAD v4: 19-36101738-G-A
• MyVariant Identifiers: chr19:g.36592640G>A (hg19) ; chr19:g.36101738G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101738G>A , CM000681.2:g.36101738G>A	GRCh38
NC_000019.9:g.36592640G>A , CM000681.1:g.36592640G>A	GRCh37
NC_000019.8:g.41284480G>A	NCBI36
NG_028101.1:g.51858G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3046G>A	ENSP00000270301.6:p.Ala1016Thr
ENST00000401500.7:c.3046G>A MANE Select	ENSP00000384792.1:p.Ala1016Thr
ENST00000587391.6:c.*2082G>A	ENSP00000465525.1:n.*2082G>A
ENST00000679357.1:c.836G>A
ENST00000679422.1:c.762-276G>A
ENST00000679682.1:c.3031G>A	ENSP00000506226.1:p.Ala1011Thr
ENST00000679714.1:c.3040G>A	ENSP00000506627.1:p.Ala1014Thr
ENST00000679757.1:c.2695G>A	ENSP00000505158.1:p.Ala899Thr
ENST00000679858.1:c.*2189G>A	ENSP00000505655.1:n.*2189G>A
ENST00000680211.1:c.-354G>A	ENSP00000506102.1:n.-354G>A
ENST00000680349.1:n.1029G>A
ENST00000680403.1:c.3046G>A	ENSP00000505677.1:p.Ala1016Thr
ENST00000680564.1:c.2971+421G>A	ENSP00000505582.1:n.2971+421G>A
ENST00000680590.1:c.*1441G>A	ENSP00000505350.1:n.*1441G>A
ENST00000680773.1:n.723G>A
ENST00000680806.1:c.*1801-276G>A	ENSP00000506418.1:n.*1801-276G>A
ENST00000680997.1:n.393G>A
ENST00000681088.1:c.708G>A
ENST00000681625.1:c.*378G>A	ENSP00000505555.1:n.*378G>A
ENST00000270301.11:c.3046G>A	ENSP00000270301.6:p.Ala1016Thr
ENST00000401500.6:c.3046G>A	ENSP00000384792.1:p.Ala1016Thr
ENST00000587391.5:c.*2082G>A	ENSP00000465525.1:n.*2082G>A
NM_001083961.1:c.3046G>A	NP_001077430.1:p.Ala1016Thr
NM_173636.4:c.3046G>A	NP_775907.4:p.Ala1016Thr
XM_005258809.2:c.2972-276G>A	XP_005258866.1:n.2972-276G>A
XM_011526837.1:c.3031G>A	XP_011525139.1:p.Ala1011Thr
XM_011526838.1:c.2971+421G>A	XP_011525140.1:n.2971+421G>A
XM_011526839.1:c.2695G>A	XP_011525141.1:p.Ala899Thr
XM_011526840.1:c.2038G>A	XP_011525142.1:p.Ala680Thr
XM_011526841.1:c.1624G>A	XP_011525143.1:p.Ala542Thr
XM_011526842.1:c.1477G>A	XP_011525144.1:p.Ala493Thr
XM_011526843.1:c.793G>A	XP_011525145.1:p.Ala265Thr
XM_011526844.1:c.793G>A	XP_011525146.1:p.Ala265Thr
XM_011526840.2:c.2038G>A	XP_011525142.1:p.Ala680Thr
XM_011526841.2:c.1624G>A	XP_011525143.1:p.Ala542Thr
XM_011526844.2:c.793G>A	XP_011525146.1:p.Ala265Thr
XM_017026665.1:c.3046G>A	XP_016882154.1:p.Ala1016Thr
NM_001083961.2:c.3046G>A MANE Select	NP_001077430.1:p.Ala1016Thr
NM_173636.5:c.3046G>A	NP_775907.4:p.Ala1016Thr