Canonical Allele Identifier: CA405460412

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104547-G-T
• MyVariant Identifiers: chr19:g.36595449G>T (hg19) ; chr19:g.36104547G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104547G>T , CM000681.2:g.36104547G>T	GRCh38
NC_000019.9:g.36595449G>T , CM000681.1:g.36595449G>T	GRCh37
NC_000019.8:g.41287289G>T	NCBI36
NG_028101.1:g.54667G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4168G>T	ENSP00000270301.6:p.Ala1390Ser
ENST00000401500.7:c.4183G>T MANE Select	ENSP00000384792.1:p.Ala1395Ser
ENST00000587391.6:c.*4043G>T	ENSP00000465525.1:n.*4043G>T
ENST00000679357.1:c.2263G>T
ENST00000679598.1:c.928G>T
ENST00000679682.1:c.4168G>T	ENSP00000506226.1:p.Ala1390Ser
ENST00000679714.1:c.4177G>T	ENSP00000506627.1:p.Ala1393Ser
ENST00000679757.1:c.3832G>T	ENSP00000505158.1:p.Ala1278Ser
ENST00000679858.1:c.*3565G>T	ENSP00000505655.1:n.*3565G>T
ENST00000680211.1:c.784G>T	ENSP00000506102.1:p.Ala262Ser
ENST00000680280.1:n.1686G>T
ENST00000680349.1:n.2832G>T
ENST00000680403.1:c.4168G>T	ENSP00000505677.1:p.Ala1390Ser
ENST00000680564.1:c.3934G>T	ENSP00000505582.1:p.Ala1312Ser
ENST00000680590.1:c.*2563G>T	ENSP00000505350.1:n.*2563G>T
ENST00000680597.1:c.916G>T
ENST00000680739.1:c.1198G>T
ENST00000680773.1:n.2684G>T
ENST00000680806.1:c.*3486G>T	ENSP00000506418.1:n.*3486G>T
ENST00000680997.1:n.2115G>T
ENST00000681608.1:n.2028G>T
ENST00000681625.1:c.*1515G>T	ENSP00000505555.1:n.*1515G>T
ENST00000681648.1:n.2234G>T
ENST00000270301.11:c.4168G>T	ENSP00000270301.6:p.Ala1390Ser
ENST00000401500.6:c.4183G>T	ENSP00000384792.1:p.Ala1395Ser
ENST00000587391.5:c.*4043G>T	ENSP00000465525.1:n.*4043G>T
NM_001083961.1:c.4183G>T	NP_001077430.1:p.Ala1395Ser
NM_173636.4:c.4168G>T	NP_775907.4:p.Ala1390Ser
XM_005258809.2:c.4072G>T	XP_005258866.1:p.Ala1358Ser
XM_011526837.1:c.4168G>T	XP_011525139.1:p.Ala1390Ser
XM_011526838.1:c.3934G>T	XP_011525140.1:p.Ala1312Ser
XM_011526839.1:c.3832G>T	XP_011525141.1:p.Ala1278Ser
XM_011526840.1:c.3175G>T	XP_011525142.1:p.Ala1059Ser
XM_011526841.1:c.2761G>T	XP_011525143.1:p.Ala921Ser
XM_011526842.1:c.2614G>T	XP_011525144.1:p.Ala872Ser
XM_011526843.1:c.1930G>T	XP_011525145.1:p.Ala644Ser
XM_011526844.1:c.1930G>T	XP_011525146.1:p.Ala644Ser
XM_011526840.2:c.3175G>T	XP_011525142.1:p.Ala1059Ser
XM_011526841.2:c.2761G>T	XP_011525143.1:p.Ala921Ser
XM_011526844.2:c.1930G>T	XP_011525146.1:p.Ala644Ser
XM_017026665.1:c.4183G>T	XP_016882154.1:p.Ala1395Ser
NM_001083961.2:c.4183G>T MANE Select	NP_001077430.1:p.Ala1395Ser
NM_173636.5:c.4168G>T	NP_775907.4:p.Ala1390Ser