Canonical Allele Identifier: CA9396505

Gene: WDR62

Linked Data

• dbSNP Id: rs566214361
• ExAC: 19:36595482 G / C
• gnomAD v2: 19-36595482-G-C
• gnomAD v4: 19-36104580-G-C
• MyVariant Identifiers: chr19:g.36595482G>C (hg19) ; chr19:g.36104580G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104580G>C , CM000681.2:g.36104580G>C	GRCh38
NC_000019.9:g.36595482G>C , CM000681.1:g.36595482G>C	GRCh37
NC_000019.8:g.41287322G>C	NCBI36
NG_028101.1:g.54700G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4201G>C	ENSP00000270301.6:p.Ala1401Pro
ENST00000401500.7:c.4216G>C MANE Select	ENSP00000384792.1:p.Ala1406Pro
ENST00000587391.6:c.*4076G>C	ENSP00000465525.1:n.*4076G>C
ENST00000679357.1:c.2296G>C
ENST00000679598.1:c.961G>C
ENST00000679682.1:c.4201G>C	ENSP00000506226.1:p.Ala1401Pro
ENST00000679714.1:c.4210G>C	ENSP00000506627.1:p.Ala1404Pro
ENST00000679757.1:c.3865G>C	ENSP00000505158.1:p.Ala1289Pro
ENST00000679858.1:c.*3598G>C	ENSP00000505655.1:n.*3598G>C
ENST00000680211.1:c.817G>C	ENSP00000506102.1:p.Ala273Pro
ENST00000680280.1:n.1719G>C
ENST00000680349.1:n.2865G>C
ENST00000680403.1:c.4201G>C	ENSP00000505677.1:p.Ala1401Pro
ENST00000680564.1:c.3967G>C	ENSP00000505582.1:p.Ala1323Pro
ENST00000680590.1:c.*2596G>C	ENSP00000505350.1:n.*2596G>C
ENST00000680597.1:c.949G>C
ENST00000680739.1:c.1231G>C
ENST00000680773.1:n.2717G>C
ENST00000680806.1:c.*3519G>C	ENSP00000506418.1:n.*3519G>C
ENST00000680997.1:n.2148G>C
ENST00000681608.1:n.2061G>C
ENST00000681625.1:c.*1548G>C	ENSP00000505555.1:n.*1548G>C
ENST00000681648.1:n.2267G>C
ENST00000270301.11:c.4201G>C	ENSP00000270301.6:p.Ala1401Pro
ENST00000401500.6:c.4216G>C	ENSP00000384792.1:p.Ala1406Pro
ENST00000587391.5:c.*4076G>C	ENSP00000465525.1:n.*4076G>C
NM_001083961.1:c.4216G>C	NP_001077430.1:p.Ala1406Pro
NM_173636.4:c.4201G>C	NP_775907.4:p.Ala1401Pro
XM_005258809.2:c.4105G>C	XP_005258866.1:p.Ala1369Pro
XM_011526837.1:c.4201G>C	XP_011525139.1:p.Ala1401Pro
XM_011526838.1:c.3967G>C	XP_011525140.1:p.Ala1323Pro
XM_011526839.1:c.3865G>C	XP_011525141.1:p.Ala1289Pro
XM_011526840.1:c.3208G>C	XP_011525142.1:p.Ala1070Pro
XM_011526841.1:c.2794G>C	XP_011525143.1:p.Ala932Pro
XM_011526842.1:c.2647G>C	XP_011525144.1:p.Ala883Pro
XM_011526843.1:c.1963G>C	XP_011525145.1:p.Ala655Pro
XM_011526844.1:c.1963G>C	XP_011525146.1:p.Ala655Pro
XM_011526840.2:c.3208G>C	XP_011525142.1:p.Ala1070Pro
XM_011526841.2:c.2794G>C	XP_011525143.1:p.Ala932Pro
XM_011526844.2:c.1963G>C	XP_011525146.1:p.Ala655Pro
XM_017026665.1:c.4216G>C	XP_016882154.1:p.Ala1406Pro
NM_001083961.2:c.4216G>C MANE Select	NP_001077430.1:p.Ala1406Pro
NM_173636.5:c.4201G>C	NP_775907.4:p.Ala1401Pro