Canonical Allele Identifier: CA405460398

Gene: WDR62

Linked Data

• dbSNP Id: rs1321813664
• gnomAD v2: 19-36595446-C-G
• gnomAD v3: 19-36104544-C-G
• gnomAD v4: 19-36104544-C-G
• MyVariant Identifiers: chr19:g.36595446C>G (hg19) ; chr19:g.36104544C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104544C>G , CM000681.2:g.36104544C>G	GRCh38
NC_000019.9:g.36595446C>G , CM000681.1:g.36595446C>G	GRCh37
NC_000019.8:g.41287286C>G	NCBI36
NG_028101.1:g.54664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4165C>G	ENSP00000270301.6:p.Pro1389Ala
ENST00000401500.7:c.4180C>G MANE Select	ENSP00000384792.1:p.Pro1394Ala
ENST00000587391.6:c.*4040C>G	ENSP00000465525.1:n.*4040C>G
ENST00000679357.1:c.2260C>G
ENST00000679598.1:c.925C>G
ENST00000679682.1:c.4165C>G	ENSP00000506226.1:p.Pro1389Ala
ENST00000679714.1:c.4174C>G	ENSP00000506627.1:p.Pro1392Ala
ENST00000679757.1:c.3829C>G	ENSP00000505158.1:p.Pro1277Ala
ENST00000679858.1:c.*3562C>G	ENSP00000505655.1:n.*3562C>G
ENST00000680211.1:c.781C>G	ENSP00000506102.1:p.Pro261Ala
ENST00000680280.1:n.1683C>G
ENST00000680349.1:n.2829C>G
ENST00000680403.1:c.4165C>G	ENSP00000505677.1:p.Pro1389Ala
ENST00000680564.1:c.3931C>G	ENSP00000505582.1:p.Pro1311Ala
ENST00000680590.1:c.*2560C>G	ENSP00000505350.1:n.*2560C>G
ENST00000680597.1:c.913C>G
ENST00000680739.1:c.1195C>G
ENST00000680773.1:n.2681C>G
ENST00000680806.1:c.*3483C>G	ENSP00000506418.1:n.*3483C>G
ENST00000680997.1:n.2112C>G
ENST00000681608.1:n.2025C>G
ENST00000681625.1:c.*1512C>G	ENSP00000505555.1:n.*1512C>G
ENST00000681648.1:n.2231C>G
ENST00000270301.11:c.4165C>G	ENSP00000270301.6:p.Pro1389Ala
ENST00000401500.6:c.4180C>G	ENSP00000384792.1:p.Pro1394Ala
ENST00000587391.5:c.*4040C>G	ENSP00000465525.1:n.*4040C>G
NM_001083961.1:c.4180C>G	NP_001077430.1:p.Pro1394Ala
NM_173636.4:c.4165C>G	NP_775907.4:p.Pro1389Ala
XM_005258809.2:c.4069C>G	XP_005258866.1:p.Pro1357Ala
XM_011526837.1:c.4165C>G	XP_011525139.1:p.Pro1389Ala
XM_011526838.1:c.3931C>G	XP_011525140.1:p.Pro1311Ala
XM_011526839.1:c.3829C>G	XP_011525141.1:p.Pro1277Ala
XM_011526840.1:c.3172C>G	XP_011525142.1:p.Pro1058Ala
XM_011526841.1:c.2758C>G	XP_011525143.1:p.Pro920Ala
XM_011526842.1:c.2611C>G	XP_011525144.1:p.Pro871Ala
XM_011526843.1:c.1927C>G	XP_011525145.1:p.Pro643Ala
XM_011526844.1:c.1927C>G	XP_011525146.1:p.Pro643Ala
XM_011526840.2:c.3172C>G	XP_011525142.1:p.Pro1058Ala
XM_011526841.2:c.2758C>G	XP_011525143.1:p.Pro920Ala
XM_011526844.2:c.1927C>G	XP_011525146.1:p.Pro643Ala
XM_017026665.1:c.4180C>G	XP_016882154.1:p.Pro1394Ala
NM_001083961.2:c.4180C>G MANE Select	NP_001077430.1:p.Pro1394Ala
NM_173636.5:c.4165C>G	NP_775907.4:p.Pro1389Ala