Canonical Allele Identifier: CA405460923

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595510G>A (hg19) ; chr19:g.36104608G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104608G>A , CM000681.2:g.36104608G>A	GRCh38
NC_000019.9:g.36595510G>A , CM000681.1:g.36595510G>A	GRCh37
NC_000019.8:g.41287350G>A	NCBI36
NG_028101.1:g.54728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4229G>A	ENSP00000270301.6:p.Ser1410Asn
ENST00000401500.7:c.4244G>A MANE Select	ENSP00000384792.1:p.Ser1415Asn
ENST00000587391.6:c.*4104G>A	ENSP00000465525.1:n.*4104G>A
ENST00000679357.1:c.2324G>A
ENST00000679598.1:c.989G>A
ENST00000679682.1:c.4229G>A	ENSP00000506226.1:p.Ser1410Asn
ENST00000679714.1:c.4238G>A	ENSP00000506627.1:p.Ser1413Asn
ENST00000679757.1:c.3893G>A	ENSP00000505158.1:p.Ser1298Asn
ENST00000679858.1:c.*3626G>A	ENSP00000505655.1:n.*3626G>A
ENST00000680211.1:c.845G>A	ENSP00000506102.1:p.Ser282Asn
ENST00000680280.1:n.1747G>A
ENST00000680349.1:n.2893G>A
ENST00000680403.1:c.4229G>A	ENSP00000505677.1:p.Ser1410Asn
ENST00000680564.1:c.3995G>A	ENSP00000505582.1:p.Ser1332Asn
ENST00000680590.1:c.*2624G>A	ENSP00000505350.1:n.*2624G>A
ENST00000680597.1:c.977G>A
ENST00000680739.1:c.1259G>A
ENST00000680773.1:n.2745G>A
ENST00000680806.1:c.*3547G>A	ENSP00000506418.1:n.*3547G>A
ENST00000680997.1:n.2176G>A
ENST00000681608.1:n.2089G>A
ENST00000681625.1:c.*1576G>A	ENSP00000505555.1:n.*1576G>A
ENST00000681648.1:n.2295G>A
ENST00000270301.11:c.4229G>A	ENSP00000270301.6:p.Ser1410Asn
ENST00000401500.6:c.4244G>A	ENSP00000384792.1:p.Ser1415Asn
ENST00000587391.5:c.*4104G>A	ENSP00000465525.1:n.*4104G>A
NM_001083961.1:c.4244G>A	NP_001077430.1:p.Ser1415Asn
NM_173636.4:c.4229G>A	NP_775907.4:p.Ser1410Asn
XM_005258809.2:c.4133G>A	XP_005258866.1:p.Ser1378Asn
XM_011526837.1:c.4229G>A	XP_011525139.1:p.Ser1410Asn
XM_011526838.1:c.3995G>A	XP_011525140.1:p.Ser1332Asn
XM_011526839.1:c.3893G>A	XP_011525141.1:p.Ser1298Asn
XM_011526840.1:c.3236G>A	XP_011525142.1:p.Ser1079Asn
XM_011526841.1:c.2822G>A	XP_011525143.1:p.Ser941Asn
XM_011526842.1:c.2675G>A	XP_011525144.1:p.Ser892Asn
XM_011526843.1:c.1991G>A	XP_011525145.1:p.Ser664Asn
XM_011526844.1:c.1991G>A	XP_011525146.1:p.Ser664Asn
XM_011526840.2:c.3236G>A	XP_011525142.1:p.Ser1079Asn
XM_011526841.2:c.2822G>A	XP_011525143.1:p.Ser941Asn
XM_011526844.2:c.1991G>A	XP_011525146.1:p.Ser664Asn
XM_017026665.1:c.4244G>A	XP_016882154.1:p.Ser1415Asn
NM_001083961.2:c.4244G>A MANE Select	NP_001077430.1:p.Ser1415Asn
NM_173636.5:c.4229G>A	NP_775907.4:p.Ser1410Asn