Canonical Allele Identifier: CA405450867

Gene: WDR62

Linked Data

• dbSNP Id: rs773422974
• gnomAD v2: 19-36593042-C-A
• gnomAD v4: 19-36102140-C-A
• MyVariant Identifiers: chr19:g.36593042C>A (hg19) ; chr19:g.36102140C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102140C>A , CM000681.2:g.36102140C>A	GRCh38
NC_000019.9:g.36593042C>A , CM000681.1:g.36593042C>A	GRCh37
NC_000019.8:g.41284882C>A	NCBI36
NG_028101.1:g.52260C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3209C>A	ENSP00000270301.6:p.Ser1070Tyr
ENST00000401500.7:c.3209C>A MANE Select	ENSP00000384792.1:p.Ser1070Tyr
ENST00000587391.6:c.*2484C>A	ENSP00000465525.1:n.*2484C>A
ENST00000679357.1:c.999C>A
ENST00000679422.1:c.888C>A
ENST00000679682.1:c.3194C>A	ENSP00000506226.1:p.Ser1065Tyr
ENST00000679714.1:c.3203C>A	ENSP00000506627.1:p.Ser1068Tyr
ENST00000679757.1:c.2858C>A	ENSP00000505158.1:p.Ser953Tyr
ENST00000679858.1:c.*2591C>A	ENSP00000505655.1:n.*2591C>A
ENST00000680211.1:c.-191C>A	ENSP00000506102.1:n.-191C>A
ENST00000680349.1:n.1192C>A
ENST00000680403.1:c.3209C>A	ENSP00000505677.1:p.Ser1070Tyr
ENST00000680564.1:c.2972-597C>A	ENSP00000505582.1:n.2972-597C>A
ENST00000680590.1:c.*1604C>A	ENSP00000505350.1:n.*1604C>A
ENST00000680739.1:c.127C>A
ENST00000680773.1:n.1125C>A
ENST00000680806.1:c.*1927C>A	ENSP00000506418.1:n.*1927C>A
ENST00000680997.1:n.556C>A
ENST00000681088.1:c.871C>A
ENST00000681608.1:n.157C>A
ENST00000681625.1:c.*541C>A	ENSP00000505555.1:n.*541C>A
ENST00000270301.11:c.3209C>A	ENSP00000270301.6:p.Ser1070Tyr
ENST00000401500.6:c.3209C>A	ENSP00000384792.1:p.Ser1070Tyr
ENST00000587391.5:c.*2484C>A	ENSP00000465525.1:n.*2484C>A
NM_001083961.1:c.3209C>A	NP_001077430.1:p.Ser1070Tyr
NM_173636.4:c.3209C>A	NP_775907.4:p.Ser1070Tyr
XM_005258809.2:c.3098C>A	XP_005258866.1:p.Ser1033Tyr
XM_011526837.1:c.3194C>A	XP_011525139.1:p.Ser1065Tyr
XM_011526838.1:c.2972-597C>A	XP_011525140.1:n.2972-597C>A
XM_011526839.1:c.2858C>A	XP_011525141.1:p.Ser953Tyr
XM_011526840.1:c.2201C>A	XP_011525142.1:p.Ser734Tyr
XM_011526841.1:c.1787C>A	XP_011525143.1:p.Ser596Tyr
XM_011526842.1:c.1640C>A	XP_011525144.1:p.Ser547Tyr
XM_011526843.1:c.956C>A	XP_011525145.1:p.Ser319Tyr
XM_011526844.1:c.956C>A	XP_011525146.1:p.Ser319Tyr
XM_011526840.2:c.2201C>A	XP_011525142.1:p.Ser734Tyr
XM_011526841.2:c.1787C>A	XP_011525143.1:p.Ser596Tyr
XM_011526844.2:c.956C>A	XP_011525146.1:p.Ser319Tyr
XM_017026665.1:c.3209C>A	XP_016882154.1:p.Ser1070Tyr
NM_001083961.2:c.3209C>A MANE Select	NP_001077430.1:p.Ser1070Tyr
NM_173636.5:c.3209C>A	NP_775907.4:p.Ser1070Tyr