Canonical Allele Identifier: CA507107521

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592959A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102057A>T , CM000681.2:g.36102057A>T	GRCh38
NC_000019.9:g.36592959A>T , CM000681.1:g.36592959A>T	GRCh37
NC_000019.8:g.41284799A>T	NCBI36
NG_028101.1:g.52177A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3126A>T	ENSP00000270301.6:p.Gly1042=
ENST00000401500.7:c.3126A>T MANE Select	ENSP00000384792.1:p.Gly1042=
ENST00000587391.6:c.*2401A>T	ENSP00000465525.1:n.*2401A>T
ENST00000679357.1:c.916A>T
ENST00000679422.1:c.805A>T
ENST00000679682.1:c.3111A>T	ENSP00000506226.1:p.Gly1037=
ENST00000679714.1:c.3120A>T	ENSP00000506627.1:p.Gly1040=
ENST00000679757.1:c.2775A>T	ENSP00000505158.1:p.Gly925=
ENST00000679858.1:c.*2508A>T	ENSP00000505655.1:n.*2508A>T
ENST00000680211.1:c.-274A>T	ENSP00000506102.1:n.-274A>T
ENST00000680349.1:n.1109A>T
ENST00000680403.1:c.3126A>T	ENSP00000505677.1:p.Gly1042=
ENST00000680564.1:c.2972-680A>T	ENSP00000505582.1:n.2972-680A>T
ENST00000680590.1:c.*1521A>T	ENSP00000505350.1:n.*1521A>T
ENST00000680739.1:c.44A>T
ENST00000680773.1:n.1042A>T
ENST00000680806.1:c.*1844A>T	ENSP00000506418.1:n.*1844A>T
ENST00000680997.1:n.473A>T
ENST00000681088.1:c.788A>T
ENST00000681608.1:n.74A>T
ENST00000681625.1:c.*458A>T	ENSP00000505555.1:n.*458A>T
ENST00000270301.11:c.3126A>T	ENSP00000270301.6:p.Gly1042=
ENST00000401500.6:c.3126A>T	ENSP00000384792.1:p.Gly1042=
ENST00000587391.5:c.*2401A>T	ENSP00000465525.1:n.*2401A>T
NM_001083961.1:c.3126A>T	NP_001077430.1:p.Gly1042=
NM_173636.4:c.3126A>T	NP_775907.4:p.Gly1042=
XM_005258809.2:c.3015A>T	XP_005258866.1:p.Gly1005=
XM_011526837.1:c.3111A>T	XP_011525139.1:p.Gly1037=
XM_011526838.1:c.2972-680A>T	XP_011525140.1:n.2972-680A>T
XM_011526839.1:c.2775A>T	XP_011525141.1:p.Gly925=
XM_011526840.1:c.2118A>T	XP_011525142.1:p.Gly706=
XM_011526841.1:c.1704A>T	XP_011525143.1:p.Gly568=
XM_011526842.1:c.1557A>T	XP_011525144.1:p.Gly519=
XM_011526843.1:c.873A>T	XP_011525145.1:p.Gly291=
XM_011526844.1:c.873A>T	XP_011525146.1:p.Gly291=
XM_011526840.2:c.2118A>T	XP_011525142.1:p.Gly706=
XM_011526841.2:c.1704A>T	XP_011525143.1:p.Gly568=
XM_011526844.2:c.873A>T	XP_011525146.1:p.Gly291=
XM_017026665.1:c.3126A>T	XP_016882154.1:p.Gly1042=
NM_001083961.2:c.3126A>T MANE Select	NP_001077430.1:p.Gly1042=
NM_173636.5:c.3126A>T	NP_775907.4:p.Gly1042=