Canonical Allele Identifier: CA405450691

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593020C>G (hg19) ; chr19:g.36102118C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102118C>G , CM000681.2:g.36102118C>G	GRCh38
NC_000019.9:g.36593020C>G , CM000681.1:g.36593020C>G	GRCh37
NC_000019.8:g.41284860C>G	NCBI36
NG_028101.1:g.52238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3187C>G	ENSP00000270301.6:p.His1063Asp
ENST00000401500.7:c.3187C>G MANE Select	ENSP00000384792.1:p.His1063Asp
ENST00000587391.6:c.*2462C>G	ENSP00000465525.1:n.*2462C>G
ENST00000679357.1:c.977C>G
ENST00000679422.1:c.866C>G
ENST00000679682.1:c.3172C>G	ENSP00000506226.1:p.His1058Asp
ENST00000679714.1:c.3181C>G	ENSP00000506627.1:p.His1061Asp
ENST00000679757.1:c.2836C>G	ENSP00000505158.1:p.His946Asp
ENST00000679858.1:c.*2569C>G	ENSP00000505655.1:n.*2569C>G
ENST00000680211.1:c.-213C>G	ENSP00000506102.1:n.-213C>G
ENST00000680349.1:n.1170C>G
ENST00000680403.1:c.3187C>G	ENSP00000505677.1:p.His1063Asp
ENST00000680564.1:c.2972-619C>G	ENSP00000505582.1:n.2972-619C>G
ENST00000680590.1:c.*1582C>G	ENSP00000505350.1:n.*1582C>G
ENST00000680739.1:c.105C>G
ENST00000680773.1:n.1103C>G
ENST00000680806.1:c.*1905C>G	ENSP00000506418.1:n.*1905C>G
ENST00000680997.1:n.534C>G
ENST00000681088.1:c.849C>G
ENST00000681608.1:n.135C>G
ENST00000681625.1:c.*519C>G	ENSP00000505555.1:n.*519C>G
ENST00000270301.11:c.3187C>G	ENSP00000270301.6:p.His1063Asp
ENST00000401500.6:c.3187C>G	ENSP00000384792.1:p.His1063Asp
ENST00000587391.5:c.*2462C>G	ENSP00000465525.1:n.*2462C>G
NM_001083961.1:c.3187C>G	NP_001077430.1:p.His1063Asp
NM_173636.4:c.3187C>G	NP_775907.4:p.His1063Asp
XM_005258809.2:c.3076C>G	XP_005258866.1:p.His1026Asp
XM_011526837.1:c.3172C>G	XP_011525139.1:p.His1058Asp
XM_011526838.1:c.2972-619C>G	XP_011525140.1:n.2972-619C>G
XM_011526839.1:c.2836C>G	XP_011525141.1:p.His946Asp
XM_011526840.1:c.2179C>G	XP_011525142.1:p.His727Asp
XM_011526841.1:c.1765C>G	XP_011525143.1:p.His589Asp
XM_011526842.1:c.1618C>G	XP_011525144.1:p.His540Asp
XM_011526843.1:c.934C>G	XP_011525145.1:p.His312Asp
XM_011526844.1:c.934C>G	XP_011525146.1:p.His312Asp
XM_011526840.2:c.2179C>G	XP_011525142.1:p.His727Asp
XM_011526841.2:c.1765C>G	XP_011525143.1:p.His589Asp
XM_011526844.2:c.934C>G	XP_011525146.1:p.His312Asp
XM_017026665.1:c.3187C>G	XP_016882154.1:p.His1063Asp
NM_001083961.2:c.3187C>G MANE Select	NP_001077430.1:p.His1063Asp
NM_173636.5:c.3187C>G	NP_775907.4:p.His1063Asp