Canonical Allele Identifier: CA507107685

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593862C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102960C>A , CM000681.2:g.36102960C>A	GRCh38
NC_000019.9:g.36593862C>A , CM000681.1:g.36593862C>A	GRCh37
NC_000019.8:g.41285702C>A	NCBI36
NG_028101.1:g.53080C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3333C>A	ENSP00000270301.6:p.Thr1111=
ENST00000401500.7:c.3348C>A MANE Select	ENSP00000384792.1:p.Thr1116=
ENST00000587391.6:c.*3208C>A	ENSP00000465525.1:n.*3208C>A
ENST00000679357.1:c.1428C>A
ENST00000679598.1:c.113C>A
ENST00000679682.1:c.3333C>A	ENSP00000506226.1:p.Thr1111=
ENST00000679714.1:c.3342C>A	ENSP00000506627.1:p.Thr1114=
ENST00000679757.1:c.2997C>A	ENSP00000505158.1:p.Thr999=
ENST00000679858.1:c.*2730C>A	ENSP00000505655.1:n.*2730C>A
ENST00000680211.1:c.-52C>A	ENSP00000506102.1:n.-52C>A
ENST00000680280.1:n.635C>A
ENST00000680349.1:n.1916C>A
ENST00000680403.1:c.3333C>A	ENSP00000505677.1:p.Thr1111=
ENST00000680564.1:c.3099C>A	ENSP00000505582.1:p.Thr1033=
ENST00000680590.1:c.*1728C>A	ENSP00000505350.1:n.*1728C>A
ENST00000680597.1:c.113C>A
ENST00000680739.1:c.363C>A
ENST00000680773.1:n.1849C>A
ENST00000680806.1:c.*2651C>A	ENSP00000506418.1:n.*2651C>A
ENST00000680997.1:n.1280C>A
ENST00000681608.1:n.977C>A
ENST00000681625.1:c.*680C>A	ENSP00000505555.1:n.*680C>A
ENST00000681648.1:n.647C>A
ENST00000270301.11:c.3333C>A	ENSP00000270301.6:p.Thr1111=
ENST00000401500.6:c.3348C>A	ENSP00000384792.1:p.Thr1116=
ENST00000587391.5:c.*3208C>A	ENSP00000465525.1:n.*3208C>A
NM_001083961.1:c.3348C>A	NP_001077430.1:p.Thr1116=
NM_173636.4:c.3333C>A	NP_775907.4:p.Thr1111=
XM_005258809.2:c.3237C>A	XP_005258866.1:p.Thr1079=
XM_011526837.1:c.3333C>A	XP_011525139.1:p.Thr1111=
XM_011526838.1:c.3099C>A	XP_011525140.1:p.Thr1033=
XM_011526839.1:c.2997C>A	XP_011525141.1:p.Thr999=
XM_011526840.1:c.2340C>A	XP_011525142.1:p.Thr780=
XM_011526841.1:c.1926C>A	XP_011525143.1:p.Thr642=
XM_011526842.1:c.1779C>A	XP_011525144.1:p.Thr593=
XM_011526843.1:c.1095C>A	XP_011525145.1:p.Thr365=
XM_011526844.1:c.1095C>A	XP_011525146.1:p.Thr365=
XM_011526840.2:c.2340C>A	XP_011525142.1:p.Thr780=
XM_011526841.2:c.1926C>A	XP_011525143.1:p.Thr642=
XM_011526844.2:c.1095C>A	XP_011525146.1:p.Thr365=
XM_017026665.1:c.3348C>A	XP_016882154.1:p.Thr1116=
NM_001083961.2:c.3348C>A MANE Select	NP_001077430.1:p.Thr1116=
NM_173636.5:c.3333C>A	NP_775907.4:p.Thr1111=