Canonical Allele Identifier: CA405449422

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592635A>T (hg19) ; chr19:g.36101733A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101733A>T , CM000681.2:g.36101733A>T	GRCh38
NC_000019.9:g.36592635A>T , CM000681.1:g.36592635A>T	GRCh37
NC_000019.8:g.41284475A>T	NCBI36
NG_028101.1:g.51853A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3041A>T	ENSP00000270301.6:p.Asp1014Val
ENST00000401500.7:c.3041A>T MANE Select	ENSP00000384792.1:p.Asp1014Val
ENST00000587391.6:c.*2077A>T	ENSP00000465525.1:n.*2077A>T
ENST00000679357.1:c.831A>T
ENST00000679422.1:c.762-281A>T
ENST00000679682.1:c.3026A>T	ENSP00000506226.1:p.Asp1009Val
ENST00000679714.1:c.3035A>T	ENSP00000506627.1:p.Asp1012Val
ENST00000679757.1:c.2690A>T	ENSP00000505158.1:p.Asp897Val
ENST00000679858.1:c.*2184A>T	ENSP00000505655.1:n.*2184A>T
ENST00000680211.1:c.-359A>T	ENSP00000506102.1:n.-359A>T
ENST00000680349.1:n.1024A>T
ENST00000680403.1:c.3041A>T	ENSP00000505677.1:p.Asp1014Val
ENST00000680564.1:c.2971+416A>T	ENSP00000505582.1:n.2971+416A>T
ENST00000680590.1:c.*1436A>T	ENSP00000505350.1:n.*1436A>T
ENST00000680773.1:n.718A>T
ENST00000680806.1:c.*1801-281A>T	ENSP00000506418.1:n.*1801-281A>T
ENST00000680997.1:n.388A>T
ENST00000681088.1:c.703A>T
ENST00000681625.1:c.*373A>T	ENSP00000505555.1:n.*373A>T
ENST00000270301.11:c.3041A>T	ENSP00000270301.6:p.Asp1014Val
ENST00000401500.6:c.3041A>T	ENSP00000384792.1:p.Asp1014Val
ENST00000587391.5:c.*2077A>T	ENSP00000465525.1:n.*2077A>T
NM_001083961.1:c.3041A>T	NP_001077430.1:p.Asp1014Val
NM_173636.4:c.3041A>T	NP_775907.4:p.Asp1014Val
XM_005258809.2:c.2972-281A>T	XP_005258866.1:n.2972-281A>T
XM_011526837.1:c.3026A>T	XP_011525139.1:p.Asp1009Val
XM_011526838.1:c.2971+416A>T	XP_011525140.1:n.2971+416A>T
XM_011526839.1:c.2690A>T	XP_011525141.1:p.Asp897Val
XM_011526840.1:c.2033A>T	XP_011525142.1:p.Asp678Val
XM_011526841.1:c.1619A>T	XP_011525143.1:p.Asp540Val
XM_011526842.1:c.1472A>T	XP_011525144.1:p.Asp491Val
XM_011526843.1:c.788A>T	XP_011525145.1:p.Asp263Val
XM_011526844.1:c.788A>T	XP_011525146.1:p.Asp263Val
XM_011526840.2:c.2033A>T	XP_011525142.1:p.Asp678Val
XM_011526841.2:c.1619A>T	XP_011525143.1:p.Asp540Val
XM_011526844.2:c.788A>T	XP_011525146.1:p.Asp263Val
XM_017026665.1:c.3041A>T	XP_016882154.1:p.Asp1014Val
NM_001083961.2:c.3041A>T MANE Select	NP_001077430.1:p.Asp1014Val
NM_173636.5:c.3041A>T	NP_775907.4:p.Asp1014Val