Canonical Allele Identifier: CA405460851

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595498C>G (hg19) ; chr19:g.36104596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104596C>G , CM000681.2:g.36104596C>G	GRCh38
NC_000019.9:g.36595498C>G , CM000681.1:g.36595498C>G	GRCh37
NC_000019.8:g.41287338C>G	NCBI36
NG_028101.1:g.54716C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4217C>G	ENSP00000270301.6:p.Pro1406Arg
ENST00000401500.7:c.4232C>G MANE Select	ENSP00000384792.1:p.Pro1411Arg
ENST00000587391.6:c.*4092C>G	ENSP00000465525.1:n.*4092C>G
ENST00000679357.1:c.2312C>G
ENST00000679598.1:c.977C>G
ENST00000679682.1:c.4217C>G	ENSP00000506226.1:p.Pro1406Arg
ENST00000679714.1:c.4226C>G	ENSP00000506627.1:p.Pro1409Arg
ENST00000679757.1:c.3881C>G	ENSP00000505158.1:p.Pro1294Arg
ENST00000679858.1:c.*3614C>G	ENSP00000505655.1:n.*3614C>G
ENST00000680211.1:c.833C>G	ENSP00000506102.1:p.Pro278Arg
ENST00000680280.1:n.1735C>G
ENST00000680349.1:n.2881C>G
ENST00000680403.1:c.4217C>G	ENSP00000505677.1:p.Pro1406Arg
ENST00000680564.1:c.3983C>G	ENSP00000505582.1:p.Pro1328Arg
ENST00000680590.1:c.*2612C>G	ENSP00000505350.1:n.*2612C>G
ENST00000680597.1:c.965C>G
ENST00000680739.1:c.1247C>G
ENST00000680773.1:n.2733C>G
ENST00000680806.1:c.*3535C>G	ENSP00000506418.1:n.*3535C>G
ENST00000680997.1:n.2164C>G
ENST00000681608.1:n.2077C>G
ENST00000681625.1:c.*1564C>G	ENSP00000505555.1:n.*1564C>G
ENST00000681648.1:n.2283C>G
ENST00000270301.11:c.4217C>G	ENSP00000270301.6:p.Pro1406Arg
ENST00000401500.6:c.4232C>G	ENSP00000384792.1:p.Pro1411Arg
ENST00000587391.5:c.*4092C>G	ENSP00000465525.1:n.*4092C>G
NM_001083961.1:c.4232C>G	NP_001077430.1:p.Pro1411Arg
NM_173636.4:c.4217C>G	NP_775907.4:p.Pro1406Arg
XM_005258809.2:c.4121C>G	XP_005258866.1:p.Pro1374Arg
XM_011526837.1:c.4217C>G	XP_011525139.1:p.Pro1406Arg
XM_011526838.1:c.3983C>G	XP_011525140.1:p.Pro1328Arg
XM_011526839.1:c.3881C>G	XP_011525141.1:p.Pro1294Arg
XM_011526840.1:c.3224C>G	XP_011525142.1:p.Pro1075Arg
XM_011526841.1:c.2810C>G	XP_011525143.1:p.Pro937Arg
XM_011526842.1:c.2663C>G	XP_011525144.1:p.Pro888Arg
XM_011526843.1:c.1979C>G	XP_011525145.1:p.Pro660Arg
XM_011526844.1:c.1979C>G	XP_011525146.1:p.Pro660Arg
XM_011526840.2:c.3224C>G	XP_011525142.1:p.Pro1075Arg
XM_011526841.2:c.2810C>G	XP_011525143.1:p.Pro937Arg
XM_011526844.2:c.1979C>G	XP_011525146.1:p.Pro660Arg
XM_017026665.1:c.4232C>G	XP_016882154.1:p.Pro1411Arg
NM_001083961.2:c.4232C>G MANE Select	NP_001077430.1:p.Pro1411Arg
NM_173636.5:c.4217C>G	NP_775907.4:p.Pro1406Arg