Canonical Allele Identifier: CA507318564

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595472G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104570G>A , CM000681.2:g.36104570G>A	GRCh38
NC_000019.9:g.36595472G>A , CM000681.1:g.36595472G>A	GRCh37
NC_000019.8:g.41287312G>A	NCBI36
NG_028101.1:g.54690G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4191G>A	ENSP00000270301.6:p.Val1397=
ENST00000401500.7:c.4206G>A MANE Select	ENSP00000384792.1:p.Val1402=
ENST00000587391.6:c.*4066G>A	ENSP00000465525.1:n.*4066G>A
ENST00000679357.1:c.2286G>A
ENST00000679598.1:c.951G>A
ENST00000679682.1:c.4191G>A	ENSP00000506226.1:p.Val1397=
ENST00000679714.1:c.4200G>A	ENSP00000506627.1:p.Val1400=
ENST00000679757.1:c.3855G>A	ENSP00000505158.1:p.Val1285=
ENST00000679858.1:c.*3588G>A	ENSP00000505655.1:n.*3588G>A
ENST00000680211.1:c.807G>A	ENSP00000506102.1:p.Val269=
ENST00000680280.1:n.1709G>A
ENST00000680349.1:n.2855G>A
ENST00000680403.1:c.4191G>A	ENSP00000505677.1:p.Val1397=
ENST00000680564.1:c.3957G>A	ENSP00000505582.1:p.Val1319=
ENST00000680590.1:c.*2586G>A	ENSP00000505350.1:n.*2586G>A
ENST00000680597.1:c.939G>A
ENST00000680739.1:c.1221G>A
ENST00000680773.1:n.2707G>A
ENST00000680806.1:c.*3509G>A	ENSP00000506418.1:n.*3509G>A
ENST00000680997.1:n.2138G>A
ENST00000681608.1:n.2051G>A
ENST00000681625.1:c.*1538G>A	ENSP00000505555.1:n.*1538G>A
ENST00000681648.1:n.2257G>A
ENST00000270301.11:c.4191G>A	ENSP00000270301.6:p.Val1397=
ENST00000401500.6:c.4206G>A	ENSP00000384792.1:p.Val1402=
ENST00000587391.5:c.*4066G>A	ENSP00000465525.1:n.*4066G>A
NM_001083961.1:c.4206G>A	NP_001077430.1:p.Val1402=
NM_173636.4:c.4191G>A	NP_775907.4:p.Val1397=
XM_005258809.2:c.4095G>A	XP_005258866.1:p.Val1365=
XM_011526837.1:c.4191G>A	XP_011525139.1:p.Val1397=
XM_011526838.1:c.3957G>A	XP_011525140.1:p.Val1319=
XM_011526839.1:c.3855G>A	XP_011525141.1:p.Val1285=
XM_011526840.1:c.3198G>A	XP_011525142.1:p.Val1066=
XM_011526841.1:c.2784G>A	XP_011525143.1:p.Val928=
XM_011526842.1:c.2637G>A	XP_011525144.1:p.Val879=
XM_011526843.1:c.1953G>A	XP_011525145.1:p.Val651=
XM_011526844.1:c.1953G>A	XP_011525146.1:p.Val651=
XM_011526840.2:c.3198G>A	XP_011525142.1:p.Val1066=
XM_011526841.2:c.2784G>A	XP_011525143.1:p.Val928=
XM_011526844.2:c.1953G>A	XP_011525146.1:p.Val651=
XM_017026665.1:c.4206G>A	XP_016882154.1:p.Val1402=
NM_001083961.2:c.4206G>A MANE Select	NP_001077430.1:p.Val1402=
NM_173636.5:c.4191G>A	NP_775907.4:p.Val1397=