Canonical Allele Identifier: CA405460785

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595494T>G (hg19) ; chr19:g.36104592T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104592T>G , CM000681.2:g.36104592T>G	GRCh38
NC_000019.9:g.36595494T>G , CM000681.1:g.36595494T>G	GRCh37
NC_000019.8:g.41287334T>G	NCBI36
NG_028101.1:g.54712T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4213T>G	ENSP00000270301.6:p.Ser1405Ala
ENST00000401500.7:c.4228T>G MANE Select	ENSP00000384792.1:p.Ser1410Ala
ENST00000587391.6:c.*4088T>G	ENSP00000465525.1:n.*4088T>G
ENST00000679357.1:c.2308T>G
ENST00000679598.1:c.973T>G
ENST00000679682.1:c.4213T>G	ENSP00000506226.1:p.Ser1405Ala
ENST00000679714.1:c.4222T>G	ENSP00000506627.1:p.Ser1408Ala
ENST00000679757.1:c.3877T>G	ENSP00000505158.1:p.Ser1293Ala
ENST00000679858.1:c.*3610T>G	ENSP00000505655.1:n.*3610T>G
ENST00000680211.1:c.829T>G	ENSP00000506102.1:p.Ser277Ala
ENST00000680280.1:n.1731T>G
ENST00000680349.1:n.2877T>G
ENST00000680403.1:c.4213T>G	ENSP00000505677.1:p.Ser1405Ala
ENST00000680564.1:c.3979T>G	ENSP00000505582.1:p.Ser1327Ala
ENST00000680590.1:c.*2608T>G	ENSP00000505350.1:n.*2608T>G
ENST00000680597.1:c.961T>G
ENST00000680739.1:c.1243T>G
ENST00000680773.1:n.2729T>G
ENST00000680806.1:c.*3531T>G	ENSP00000506418.1:n.*3531T>G
ENST00000680997.1:n.2160T>G
ENST00000681608.1:n.2073T>G
ENST00000681625.1:c.*1560T>G	ENSP00000505555.1:n.*1560T>G
ENST00000681648.1:n.2279T>G
ENST00000270301.11:c.4213T>G	ENSP00000270301.6:p.Ser1405Ala
ENST00000401500.6:c.4228T>G	ENSP00000384792.1:p.Ser1410Ala
ENST00000587391.5:c.*4088T>G	ENSP00000465525.1:n.*4088T>G
NM_001083961.1:c.4228T>G	NP_001077430.1:p.Ser1410Ala
NM_173636.4:c.4213T>G	NP_775907.4:p.Ser1405Ala
XM_005258809.2:c.4117T>G	XP_005258866.1:p.Ser1373Ala
XM_011526837.1:c.4213T>G	XP_011525139.1:p.Ser1405Ala
XM_011526838.1:c.3979T>G	XP_011525140.1:p.Ser1327Ala
XM_011526839.1:c.3877T>G	XP_011525141.1:p.Ser1293Ala
XM_011526840.1:c.3220T>G	XP_011525142.1:p.Ser1074Ala
XM_011526841.1:c.2806T>G	XP_011525143.1:p.Ser936Ala
XM_011526842.1:c.2659T>G	XP_011525144.1:p.Ser887Ala
XM_011526843.1:c.1975T>G	XP_011525145.1:p.Ser659Ala
XM_011526844.1:c.1975T>G	XP_011525146.1:p.Ser659Ala
XM_011526840.2:c.3220T>G	XP_011525142.1:p.Ser1074Ala
XM_011526841.2:c.2806T>G	XP_011525143.1:p.Ser936Ala
XM_011526844.2:c.1975T>G	XP_011525146.1:p.Ser659Ala
XM_017026665.1:c.4228T>G	XP_016882154.1:p.Ser1410Ala
NM_001083961.2:c.4228T>G MANE Select	NP_001077430.1:p.Ser1410Ala
NM_173636.5:c.4213T>G	NP_775907.4:p.Ser1405Ala