Canonical Allele Identifier: CA507107003

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101692-G-A
• MyVariant Identifiers: chr19:g.36592594G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101692G>A , CM000681.2:g.36101692G>A	GRCh38
NC_000019.9:g.36592594G>A , CM000681.1:g.36592594G>A	GRCh37
NC_000019.8:g.41284434G>A	NCBI36
NG_028101.1:g.51812G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3000G>A	ENSP00000270301.6:p.Glu1000=
ENST00000401500.7:c.3000G>A MANE Select	ENSP00000384792.1:p.Glu1000=
ENST00000587391.6:c.*2036G>A	ENSP00000465525.1:n.*2036G>A
ENST00000679357.1:c.790G>A
ENST00000679422.1:c.762-322G>A
ENST00000679682.1:c.2985G>A	ENSP00000506226.1:p.Glu995=
ENST00000679714.1:c.2994G>A	ENSP00000506627.1:p.Glu998=
ENST00000679757.1:c.2649G>A	ENSP00000505158.1:p.Glu883=
ENST00000679858.1:c.*2143G>A	ENSP00000505655.1:n.*2143G>A
ENST00000680211.1:c.-400G>A	ENSP00000506102.1:n.-400G>A
ENST00000680349.1:n.983G>A
ENST00000680403.1:c.3000G>A	ENSP00000505677.1:p.Glu1000=
ENST00000680564.1:c.2971+375G>A	ENSP00000505582.1:n.2971+375G>A
ENST00000680590.1:c.*1395G>A	ENSP00000505350.1:n.*1395G>A
ENST00000680773.1:n.677G>A
ENST00000680806.1:c.*1801-322G>A	ENSP00000506418.1:n.*1801-322G>A
ENST00000680997.1:n.347G>A
ENST00000681088.1:c.662G>A
ENST00000681625.1:c.*332G>A	ENSP00000505555.1:n.*332G>A
ENST00000270301.11:c.3000G>A	ENSP00000270301.6:p.Glu1000=
ENST00000401500.6:c.3000G>A	ENSP00000384792.1:p.Glu1000=
ENST00000587391.5:c.*2036G>A	ENSP00000465525.1:n.*2036G>A
NM_001083961.1:c.3000G>A	NP_001077430.1:p.Glu1000=
NM_173636.4:c.3000G>A	NP_775907.4:p.Glu1000=
XM_005258809.2:c.2972-322G>A	XP_005258866.1:n.2972-322G>A
XM_011526837.1:c.2985G>A	XP_011525139.1:p.Glu995=
XM_011526838.1:c.2971+375G>A	XP_011525140.1:n.2971+375G>A
XM_011526839.1:c.2649G>A	XP_011525141.1:p.Glu883=
XM_011526840.1:c.1992G>A	XP_011525142.1:p.Glu664=
XM_011526841.1:c.1578G>A	XP_011525143.1:p.Glu526=
XM_011526842.1:c.1431G>A	XP_011525144.1:p.Glu477=
XM_011526843.1:c.747G>A	XP_011525145.1:p.Glu249=
XM_011526844.1:c.747G>A	XP_011525146.1:p.Glu249=
XM_011526840.2:c.1992G>A	XP_011525142.1:p.Glu664=
XM_011526841.2:c.1578G>A	XP_011525143.1:p.Glu526=
XM_011526844.2:c.747G>A	XP_011525146.1:p.Glu249=
XM_017026665.1:c.3000G>A	XP_016882154.1:p.Glu1000=
NM_001083961.2:c.3000G>A MANE Select	NP_001077430.1:p.Glu1000=
NM_173636.5:c.3000G>A	NP_775907.4:p.Glu1000=