Canonical Allele Identifier: CA507107498

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592932A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102030A>C , CM000681.2:g.36102030A>C	GRCh38
NC_000019.9:g.36592932A>C , CM000681.1:g.36592932A>C	GRCh37
NC_000019.8:g.41284772A>C	NCBI36
NG_028101.1:g.52150A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3099A>C	ENSP00000270301.6:p.Thr1033=
ENST00000401500.7:c.3099A>C MANE Select	ENSP00000384792.1:p.Thr1033=
ENST00000587391.6:c.*2374A>C	ENSP00000465525.1:n.*2374A>C
ENST00000679357.1:c.889A>C
ENST00000679422.1:c.778A>C
ENST00000679682.1:c.3084A>C	ENSP00000506226.1:p.Thr1028=
ENST00000679714.1:c.3093A>C	ENSP00000506627.1:p.Thr1031=
ENST00000679757.1:c.2748A>C	ENSP00000505158.1:p.Thr916=
ENST00000679858.1:c.*2481A>C	ENSP00000505655.1:n.*2481A>C
ENST00000680211.1:c.-301A>C	ENSP00000506102.1:n.-301A>C
ENST00000680349.1:n.1082A>C
ENST00000680403.1:c.3099A>C	ENSP00000505677.1:p.Thr1033=
ENST00000680564.1:c.2972-707A>C	ENSP00000505582.1:n.2972-707A>C
ENST00000680590.1:c.*1494A>C	ENSP00000505350.1:n.*1494A>C
ENST00000680739.1:c.17A>C
ENST00000680773.1:n.1015A>C
ENST00000680806.1:c.*1817A>C	ENSP00000506418.1:n.*1817A>C
ENST00000680997.1:n.446A>C
ENST00000681088.1:c.761A>C
ENST00000681608.1:n.47A>C
ENST00000681625.1:c.*431A>C	ENSP00000505555.1:n.*431A>C
ENST00000270301.11:c.3099A>C	ENSP00000270301.6:p.Thr1033=
ENST00000401500.6:c.3099A>C	ENSP00000384792.1:p.Thr1033=
ENST00000587391.5:c.*2374A>C	ENSP00000465525.1:n.*2374A>C
NM_001083961.1:c.3099A>C	NP_001077430.1:p.Thr1033=
NM_173636.4:c.3099A>C	NP_775907.4:p.Thr1033=
XM_005258809.2:c.2988A>C	XP_005258866.1:p.Thr996=
XM_011526837.1:c.3084A>C	XP_011525139.1:p.Thr1028=
XM_011526838.1:c.2972-707A>C	XP_011525140.1:n.2972-707A>C
XM_011526839.1:c.2748A>C	XP_011525141.1:p.Thr916=
XM_011526840.1:c.2091A>C	XP_011525142.1:p.Thr697=
XM_011526841.1:c.1677A>C	XP_011525143.1:p.Thr559=
XM_011526842.1:c.1530A>C	XP_011525144.1:p.Thr510=
XM_011526843.1:c.846A>C	XP_011525145.1:p.Thr282=
XM_011526844.1:c.846A>C	XP_011525146.1:p.Thr282=
XM_011526840.2:c.2091A>C	XP_011525142.1:p.Thr697=
XM_011526841.2:c.1677A>C	XP_011525143.1:p.Thr559=
XM_011526844.2:c.846A>C	XP_011525146.1:p.Thr282=
XM_017026665.1:c.3099A>C	XP_016882154.1:p.Thr1033=
NM_001083961.2:c.3099A>C MANE Select	NP_001077430.1:p.Thr1033=
NM_173636.5:c.3099A>C	NP_775907.4:p.Thr1033=