Canonical Allele Identifier: CA405449957

Gene: WDR62

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3097A>T	ENSP00000270301.6:p.Thr1033Ser
ENST00000401500.7:c.3097A>T MANE Select	ENSP00000384792.1:p.Thr1033Ser
ENST00000587391.6:c.*2372A>T	ENSP00000465525.1:n.*2372A>T
ENST00000679357.1:c.887A>T
ENST00000679422.1:c.776A>T
ENST00000679682.1:c.3082A>T	ENSP00000506226.1:p.Thr1028Ser
ENST00000679714.1:c.3091A>T	ENSP00000506627.1:p.Thr1031Ser
ENST00000679757.1:c.2746A>T	ENSP00000505158.1:p.Thr916Ser
ENST00000679858.1:c.*2479A>T	ENSP00000505655.1:n.*2479A>T
ENST00000680211.1:c.-303A>T	ENSP00000506102.1:n.-303A>T
ENST00000680349.1:n.1080A>T
ENST00000680403.1:c.3097A>T	ENSP00000505677.1:p.Thr1033Ser
ENST00000680564.1:c.2972-709A>T	ENSP00000505582.1:n.2972-709A>T
ENST00000680590.1:c.*1492A>T	ENSP00000505350.1:n.*1492A>T
ENST00000680739.1:c.15A>T
ENST00000680773.1:n.1013A>T
ENST00000680806.1:c.*1815A>T	ENSP00000506418.1:n.*1815A>T
ENST00000680997.1:n.444A>T
ENST00000681088.1:c.759A>T
ENST00000681608.1:n.45A>T
ENST00000681625.1:c.*429A>T	ENSP00000505555.1:n.*429A>T
ENST00000270301.11:c.3097A>T	ENSP00000270301.6:p.Thr1033Ser
ENST00000401500.6:c.3097A>T	ENSP00000384792.1:p.Thr1033Ser
ENST00000587391.5:c.*2372A>T	ENSP00000465525.1:n.*2372A>T
NM_001083961.1:c.3097A>T	NP_001077430.1:p.Thr1033Ser
NM_173636.4:c.3097A>T	NP_775907.4:p.Thr1033Ser
XM_005258809.2:c.2986A>T	XP_005258866.1:p.Thr996Ser
XM_011526837.1:c.3082A>T	XP_011525139.1:p.Thr1028Ser
XM_011526838.1:c.2972-709A>T	XP_011525140.1:n.2972-709A>T
XM_011526839.1:c.2746A>T	XP_011525141.1:p.Thr916Ser
XM_011526840.1:c.2089A>T	XP_011525142.1:p.Thr697Ser
XM_011526841.1:c.1675A>T	XP_011525143.1:p.Thr559Ser
XM_011526842.1:c.1528A>T	XP_011525144.1:p.Thr510Ser
XM_011526843.1:c.844A>T	XP_011525145.1:p.Thr282Ser
XM_011526844.1:c.844A>T	XP_011525146.1:p.Thr282Ser
XM_011526840.2:c.2089A>T	XP_011525142.1:p.Thr697Ser
XM_011526841.2:c.1675A>T	XP_011525143.1:p.Thr559Ser
XM_011526844.2:c.844A>T	XP_011525146.1:p.Thr282Ser
XM_017026665.1:c.3097A>T	XP_016882154.1:p.Thr1033Ser
NM_001083961.2:c.3097A>T MANE Select	NP_001077430.1:p.Thr1033Ser
NM_173636.5:c.3097A>T	NP_775907.4:p.Thr1033Ser