Canonical Allele Identifier: CA405450133

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592955A>T (hg19) ; chr19:g.36102053A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102053A>T , CM000681.2:g.36102053A>T	GRCh38
NC_000019.9:g.36592955A>T , CM000681.1:g.36592955A>T	GRCh37
NC_000019.8:g.41284795A>T	NCBI36
NG_028101.1:g.52173A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3122A>T	ENSP00000270301.6:p.Glu1041Val
ENST00000401500.7:c.3122A>T MANE Select	ENSP00000384792.1:p.Glu1041Val
ENST00000587391.6:c.*2397A>T	ENSP00000465525.1:n.*2397A>T
ENST00000679357.1:c.912A>T
ENST00000679422.1:c.801A>T
ENST00000679682.1:c.3107A>T	ENSP00000506226.1:p.Glu1036Val
ENST00000679714.1:c.3116A>T	ENSP00000506627.1:p.Glu1039Val
ENST00000679757.1:c.2771A>T	ENSP00000505158.1:p.Glu924Val
ENST00000679858.1:c.*2504A>T	ENSP00000505655.1:n.*2504A>T
ENST00000680211.1:c.-278A>T	ENSP00000506102.1:n.-278A>T
ENST00000680349.1:n.1105A>T
ENST00000680403.1:c.3122A>T	ENSP00000505677.1:p.Glu1041Val
ENST00000680564.1:c.2972-684A>T	ENSP00000505582.1:n.2972-684A>T
ENST00000680590.1:c.*1517A>T	ENSP00000505350.1:n.*1517A>T
ENST00000680739.1:c.40A>T
ENST00000680773.1:n.1038A>T
ENST00000680806.1:c.*1840A>T	ENSP00000506418.1:n.*1840A>T
ENST00000680997.1:n.469A>T
ENST00000681088.1:c.784A>T
ENST00000681608.1:n.70A>T
ENST00000681625.1:c.*454A>T	ENSP00000505555.1:n.*454A>T
ENST00000270301.11:c.3122A>T	ENSP00000270301.6:p.Glu1041Val
ENST00000401500.6:c.3122A>T	ENSP00000384792.1:p.Glu1041Val
ENST00000587391.5:c.*2397A>T	ENSP00000465525.1:n.*2397A>T
NM_001083961.1:c.3122A>T	NP_001077430.1:p.Glu1041Val
NM_173636.4:c.3122A>T	NP_775907.4:p.Glu1041Val
XM_005258809.2:c.3011A>T	XP_005258866.1:p.Glu1004Val
XM_011526837.1:c.3107A>T	XP_011525139.1:p.Glu1036Val
XM_011526838.1:c.2972-684A>T	XP_011525140.1:n.2972-684A>T
XM_011526839.1:c.2771A>T	XP_011525141.1:p.Glu924Val
XM_011526840.1:c.2114A>T	XP_011525142.1:p.Glu705Val
XM_011526841.1:c.1700A>T	XP_011525143.1:p.Glu567Val
XM_011526842.1:c.1553A>T	XP_011525144.1:p.Glu518Val
XM_011526843.1:c.869A>T	XP_011525145.1:p.Glu290Val
XM_011526844.1:c.869A>T	XP_011525146.1:p.Glu290Val
XM_011526840.2:c.2114A>T	XP_011525142.1:p.Glu705Val
XM_011526841.2:c.1700A>T	XP_011525143.1:p.Glu567Val
XM_011526844.2:c.869A>T	XP_011525146.1:p.Glu290Val
XM_017026665.1:c.3122A>T	XP_016882154.1:p.Glu1041Val
NM_001083961.2:c.3122A>T MANE Select	NP_001077430.1:p.Glu1041Val
NM_173636.5:c.3122A>T	NP_775907.4:p.Glu1041Val