Canonical Allele Identifier: CA405449507

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592646C>G (hg19) ; chr19:g.36101744C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101744C>G , CM000681.2:g.36101744C>G	GRCh38
NC_000019.9:g.36592646C>G , CM000681.1:g.36592646C>G	GRCh37
NC_000019.8:g.41284486C>G	NCBI36
NG_028101.1:g.51864C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3052C>G	ENSP00000270301.6:p.Arg1018Gly
ENST00000401500.7:c.3052C>G MANE Select	ENSP00000384792.1:p.Arg1018Gly
ENST00000587391.6:c.*2088C>G	ENSP00000465525.1:n.*2088C>G
ENST00000679357.1:c.842C>G
ENST00000679422.1:c.762-270C>G
ENST00000679682.1:c.3037C>G	ENSP00000506226.1:p.Arg1013Gly
ENST00000679714.1:c.3046C>G	ENSP00000506627.1:p.Arg1016Gly
ENST00000679757.1:c.2701C>G	ENSP00000505158.1:p.Arg901Gly
ENST00000679858.1:c.*2195C>G	ENSP00000505655.1:n.*2195C>G
ENST00000680211.1:c.-348C>G	ENSP00000506102.1:n.-348C>G
ENST00000680349.1:n.1035C>G
ENST00000680403.1:c.3052C>G	ENSP00000505677.1:p.Arg1018Gly
ENST00000680564.1:c.2971+427C>G	ENSP00000505582.1:n.2971+427C>G
ENST00000680590.1:c.*1447C>G	ENSP00000505350.1:n.*1447C>G
ENST00000680773.1:n.729C>G
ENST00000680806.1:c.*1801-270C>G	ENSP00000506418.1:n.*1801-270C>G
ENST00000680997.1:n.399C>G
ENST00000681088.1:c.714C>G
ENST00000681625.1:c.*384C>G	ENSP00000505555.1:n.*384C>G
ENST00000270301.11:c.3052C>G	ENSP00000270301.6:p.Arg1018Gly
ENST00000401500.6:c.3052C>G	ENSP00000384792.1:p.Arg1018Gly
ENST00000587391.5:c.*2088C>G	ENSP00000465525.1:n.*2088C>G
NM_001083961.1:c.3052C>G	NP_001077430.1:p.Arg1018Gly
NM_173636.4:c.3052C>G	NP_775907.4:p.Arg1018Gly
XM_005258809.2:c.2972-270C>G	XP_005258866.1:n.2972-270C>G
XM_011526837.1:c.3037C>G	XP_011525139.1:p.Arg1013Gly
XM_011526838.1:c.2971+427C>G	XP_011525140.1:n.2971+427C>G
XM_011526839.1:c.2701C>G	XP_011525141.1:p.Arg901Gly
XM_011526840.1:c.2044C>G	XP_011525142.1:p.Arg682Gly
XM_011526841.1:c.1630C>G	XP_011525143.1:p.Arg544Gly
XM_011526842.1:c.1483C>G	XP_011525144.1:p.Arg495Gly
XM_011526843.1:c.799C>G	XP_011525145.1:p.Arg267Gly
XM_011526844.1:c.799C>G	XP_011525146.1:p.Arg267Gly
XM_011526840.2:c.2044C>G	XP_011525142.1:p.Arg682Gly
XM_011526841.2:c.1630C>G	XP_011525143.1:p.Arg544Gly
XM_011526844.2:c.799C>G	XP_011525146.1:p.Arg267Gly
XM_017026665.1:c.3052C>G	XP_016882154.1:p.Arg1018Gly
NM_001083961.2:c.3052C>G MANE Select	NP_001077430.1:p.Arg1018Gly
NM_173636.5:c.3052C>G	NP_775907.4:p.Arg1018Gly