Canonical Allele Identifier: CA405449954

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592930A>C (hg19) ; chr19:g.36102028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102028A>C , CM000681.2:g.36102028A>C	GRCh38
NC_000019.9:g.36592930A>C , CM000681.1:g.36592930A>C	GRCh37
NC_000019.8:g.41284770A>C	NCBI36
NG_028101.1:g.52148A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3097A>C	ENSP00000270301.6:p.Thr1033Pro
ENST00000401500.7:c.3097A>C MANE Select	ENSP00000384792.1:p.Thr1033Pro
ENST00000587391.6:c.*2372A>C	ENSP00000465525.1:n.*2372A>C
ENST00000679357.1:c.887A>C
ENST00000679422.1:c.776A>C
ENST00000679682.1:c.3082A>C	ENSP00000506226.1:p.Thr1028Pro
ENST00000679714.1:c.3091A>C	ENSP00000506627.1:p.Thr1031Pro
ENST00000679757.1:c.2746A>C	ENSP00000505158.1:p.Thr916Pro
ENST00000679858.1:c.*2479A>C	ENSP00000505655.1:n.*2479A>C
ENST00000680211.1:c.-303A>C	ENSP00000506102.1:n.-303A>C
ENST00000680349.1:n.1080A>C
ENST00000680403.1:c.3097A>C	ENSP00000505677.1:p.Thr1033Pro
ENST00000680564.1:c.2972-709A>C	ENSP00000505582.1:n.2972-709A>C
ENST00000680590.1:c.*1492A>C	ENSP00000505350.1:n.*1492A>C
ENST00000680739.1:c.15A>C
ENST00000680773.1:n.1013A>C
ENST00000680806.1:c.*1815A>C	ENSP00000506418.1:n.*1815A>C
ENST00000680997.1:n.444A>C
ENST00000681088.1:c.759A>C
ENST00000681608.1:n.45A>C
ENST00000681625.1:c.*429A>C	ENSP00000505555.1:n.*429A>C
ENST00000270301.11:c.3097A>C	ENSP00000270301.6:p.Thr1033Pro
ENST00000401500.6:c.3097A>C	ENSP00000384792.1:p.Thr1033Pro
ENST00000587391.5:c.*2372A>C	ENSP00000465525.1:n.*2372A>C
NM_001083961.1:c.3097A>C	NP_001077430.1:p.Thr1033Pro
NM_173636.4:c.3097A>C	NP_775907.4:p.Thr1033Pro
XM_005258809.2:c.2986A>C	XP_005258866.1:p.Thr996Pro
XM_011526837.1:c.3082A>C	XP_011525139.1:p.Thr1028Pro
XM_011526838.1:c.2972-709A>C	XP_011525140.1:n.2972-709A>C
XM_011526839.1:c.2746A>C	XP_011525141.1:p.Thr916Pro
XM_011526840.1:c.2089A>C	XP_011525142.1:p.Thr697Pro
XM_011526841.1:c.1675A>C	XP_011525143.1:p.Thr559Pro
XM_011526842.1:c.1528A>C	XP_011525144.1:p.Thr510Pro
XM_011526843.1:c.844A>C	XP_011525145.1:p.Thr282Pro
XM_011526844.1:c.844A>C	XP_011525146.1:p.Thr282Pro
XM_011526840.2:c.2089A>C	XP_011525142.1:p.Thr697Pro
XM_011526841.2:c.1675A>C	XP_011525143.1:p.Thr559Pro
XM_011526844.2:c.844A>C	XP_011525146.1:p.Thr282Pro
XM_017026665.1:c.3097A>C	XP_016882154.1:p.Thr1033Pro
NM_001083961.2:c.3097A>C MANE Select	NP_001077430.1:p.Thr1033Pro
NM_173636.5:c.3097A>C	NP_775907.4:p.Thr1033Pro