Canonical Allele Identifier: CA507107581

Gene: WDR62

Linked Data

• dbSNP Id: rs1973390270
• gnomAD v4: 19-36102114-C-A
• MyVariant Identifiers: chr19:g.36593016C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102114C>A , CM000681.2:g.36102114C>A	GRCh38
NC_000019.9:g.36593016C>A , CM000681.1:g.36593016C>A	GRCh37
NC_000019.8:g.41284856C>A	NCBI36
NG_028101.1:g.52234C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3183C>A	ENSP00000270301.6:p.Arg1061=
ENST00000401500.7:c.3183C>A MANE Select	ENSP00000384792.1:p.Arg1061=
ENST00000587391.6:c.*2458C>A	ENSP00000465525.1:n.*2458C>A
ENST00000679357.1:c.973C>A
ENST00000679422.1:c.862C>A
ENST00000679682.1:c.3168C>A	ENSP00000506226.1:p.Arg1056=
ENST00000679714.1:c.3177C>A	ENSP00000506627.1:p.Arg1059=
ENST00000679757.1:c.2832C>A	ENSP00000505158.1:p.Arg944=
ENST00000679858.1:c.*2565C>A	ENSP00000505655.1:n.*2565C>A
ENST00000680211.1:c.-217C>A	ENSP00000506102.1:n.-217C>A
ENST00000680349.1:n.1166C>A
ENST00000680403.1:c.3183C>A	ENSP00000505677.1:p.Arg1061=
ENST00000680564.1:c.2972-623C>A	ENSP00000505582.1:n.2972-623C>A
ENST00000680590.1:c.*1578C>A	ENSP00000505350.1:n.*1578C>A
ENST00000680739.1:c.101C>A
ENST00000680773.1:n.1099C>A
ENST00000680806.1:c.*1901C>A	ENSP00000506418.1:n.*1901C>A
ENST00000680997.1:n.530C>A
ENST00000681088.1:c.845C>A
ENST00000681608.1:n.131C>A
ENST00000681625.1:c.*515C>A	ENSP00000505555.1:n.*515C>A
ENST00000270301.11:c.3183C>A	ENSP00000270301.6:p.Arg1061=
ENST00000401500.6:c.3183C>A	ENSP00000384792.1:p.Arg1061=
ENST00000587391.5:c.*2458C>A	ENSP00000465525.1:n.*2458C>A
NM_001083961.1:c.3183C>A	NP_001077430.1:p.Arg1061=
NM_173636.4:c.3183C>A	NP_775907.4:p.Arg1061=
XM_005258809.2:c.3072C>A	XP_005258866.1:p.Arg1024=
XM_011526837.1:c.3168C>A	XP_011525139.1:p.Arg1056=
XM_011526838.1:c.2972-623C>A	XP_011525140.1:n.2972-623C>A
XM_011526839.1:c.2832C>A	XP_011525141.1:p.Arg944=
XM_011526840.1:c.2175C>A	XP_011525142.1:p.Arg725=
XM_011526841.1:c.1761C>A	XP_011525143.1:p.Arg587=
XM_011526842.1:c.1614C>A	XP_011525144.1:p.Arg538=
XM_011526843.1:c.930C>A	XP_011525145.1:p.Arg310=
XM_011526844.1:c.930C>A	XP_011525146.1:p.Arg310=
XM_011526840.2:c.2175C>A	XP_011525142.1:p.Arg725=
XM_011526841.2:c.1761C>A	XP_011525143.1:p.Arg587=
XM_011526844.2:c.930C>A	XP_011525146.1:p.Arg310=
XM_017026665.1:c.3183C>A	XP_016882154.1:p.Arg1061=
NM_001083961.2:c.3183C>A MANE Select	NP_001077430.1:p.Arg1061=
NM_173636.5:c.3183C>A	NP_775907.4:p.Arg1061=