Canonical Allele Identifier: CA405450306

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102077-C-G
• MyVariant Identifiers: chr19:g.36592979C>G (hg19) ; chr19:g.36102077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102077C>G , CM000681.2:g.36102077C>G	GRCh38
NC_000019.9:g.36592979C>G , CM000681.1:g.36592979C>G	GRCh37
NC_000019.8:g.41284819C>G	NCBI36
NG_028101.1:g.52197C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3146C>G	ENSP00000270301.6:p.Ser1049Cys
ENST00000401500.7:c.3146C>G MANE Select	ENSP00000384792.1:p.Ser1049Cys
ENST00000587391.6:c.*2421C>G	ENSP00000465525.1:n.*2421C>G
ENST00000679357.1:c.936C>G
ENST00000679422.1:c.825C>G
ENST00000679682.1:c.3131C>G	ENSP00000506226.1:p.Ser1044Cys
ENST00000679714.1:c.3140C>G	ENSP00000506627.1:p.Ser1047Cys
ENST00000679757.1:c.2795C>G	ENSP00000505158.1:p.Ser932Cys
ENST00000679858.1:c.*2528C>G	ENSP00000505655.1:n.*2528C>G
ENST00000680211.1:c.-254C>G	ENSP00000506102.1:n.-254C>G
ENST00000680349.1:n.1129C>G
ENST00000680403.1:c.3146C>G	ENSP00000505677.1:p.Ser1049Cys
ENST00000680564.1:c.2972-660C>G	ENSP00000505582.1:n.2972-660C>G
ENST00000680590.1:c.*1541C>G	ENSP00000505350.1:n.*1541C>G
ENST00000680739.1:c.64C>G
ENST00000680773.1:n.1062C>G
ENST00000680806.1:c.*1864C>G	ENSP00000506418.1:n.*1864C>G
ENST00000680997.1:n.493C>G
ENST00000681088.1:c.808C>G
ENST00000681608.1:n.94C>G
ENST00000681625.1:c.*478C>G	ENSP00000505555.1:n.*478C>G
ENST00000270301.11:c.3146C>G	ENSP00000270301.6:p.Ser1049Cys
ENST00000401500.6:c.3146C>G	ENSP00000384792.1:p.Ser1049Cys
ENST00000587391.5:c.*2421C>G	ENSP00000465525.1:n.*2421C>G
NM_001083961.1:c.3146C>G	NP_001077430.1:p.Ser1049Cys
NM_173636.4:c.3146C>G	NP_775907.4:p.Ser1049Cys
XM_005258809.2:c.3035C>G	XP_005258866.1:p.Ser1012Cys
XM_011526837.1:c.3131C>G	XP_011525139.1:p.Ser1044Cys
XM_011526838.1:c.2972-660C>G	XP_011525140.1:n.2972-660C>G
XM_011526839.1:c.2795C>G	XP_011525141.1:p.Ser932Cys
XM_011526840.1:c.2138C>G	XP_011525142.1:p.Ser713Cys
XM_011526841.1:c.1724C>G	XP_011525143.1:p.Ser575Cys
XM_011526842.1:c.1577C>G	XP_011525144.1:p.Ser526Cys
XM_011526843.1:c.893C>G	XP_011525145.1:p.Ser298Cys
XM_011526844.1:c.893C>G	XP_011525146.1:p.Ser298Cys
XM_011526840.2:c.2138C>G	XP_011525142.1:p.Ser713Cys
XM_011526841.2:c.1724C>G	XP_011525143.1:p.Ser575Cys
XM_011526844.2:c.893C>G	XP_011525146.1:p.Ser298Cys
XM_017026665.1:c.3146C>G	XP_016882154.1:p.Ser1049Cys
NM_001083961.2:c.3146C>G MANE Select	NP_001077430.1:p.Ser1049Cys
NM_173636.5:c.3146C>G	NP_775907.4:p.Ser1049Cys