Canonical Allele Identifier: CA507318591

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595484C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104582C>A , CM000681.2:g.36104582C>A	GRCh38
NC_000019.9:g.36595484C>A , CM000681.1:g.36595484C>A	GRCh37
NC_000019.8:g.41287324C>A	NCBI36
NG_028101.1:g.54702C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4203C>A	ENSP00000270301.6:p.Ala1401=
ENST00000401500.7:c.4218C>A MANE Select	ENSP00000384792.1:p.Ala1406=
ENST00000587391.6:c.*4078C>A	ENSP00000465525.1:n.*4078C>A
ENST00000679357.1:c.2298C>A
ENST00000679598.1:c.963C>A
ENST00000679682.1:c.4203C>A	ENSP00000506226.1:p.Ala1401=
ENST00000679714.1:c.4212C>A	ENSP00000506627.1:p.Ala1404=
ENST00000679757.1:c.3867C>A	ENSP00000505158.1:p.Ala1289=
ENST00000679858.1:c.*3600C>A	ENSP00000505655.1:n.*3600C>A
ENST00000680211.1:c.819C>A	ENSP00000506102.1:p.Ala273=
ENST00000680280.1:n.1721C>A
ENST00000680349.1:n.2867C>A
ENST00000680403.1:c.4203C>A	ENSP00000505677.1:p.Ala1401=
ENST00000680564.1:c.3969C>A	ENSP00000505582.1:p.Ala1323=
ENST00000680590.1:c.*2598C>A	ENSP00000505350.1:n.*2598C>A
ENST00000680597.1:c.951C>A
ENST00000680739.1:c.1233C>A
ENST00000680773.1:n.2719C>A
ENST00000680806.1:c.*3521C>A	ENSP00000506418.1:n.*3521C>A
ENST00000680997.1:n.2150C>A
ENST00000681608.1:n.2063C>A
ENST00000681625.1:c.*1550C>A	ENSP00000505555.1:n.*1550C>A
ENST00000681648.1:n.2269C>A
ENST00000270301.11:c.4203C>A	ENSP00000270301.6:p.Ala1401=
ENST00000401500.6:c.4218C>A	ENSP00000384792.1:p.Ala1406=
ENST00000587391.5:c.*4078C>A	ENSP00000465525.1:n.*4078C>A
NM_001083961.1:c.4218C>A	NP_001077430.1:p.Ala1406=
NM_173636.4:c.4203C>A	NP_775907.4:p.Ala1401=
XM_005258809.2:c.4107C>A	XP_005258866.1:p.Ala1369=
XM_011526837.1:c.4203C>A	XP_011525139.1:p.Ala1401=
XM_011526838.1:c.3969C>A	XP_011525140.1:p.Ala1323=
XM_011526839.1:c.3867C>A	XP_011525141.1:p.Ala1289=
XM_011526840.1:c.3210C>A	XP_011525142.1:p.Ala1070=
XM_011526841.1:c.2796C>A	XP_011525143.1:p.Ala932=
XM_011526842.1:c.2649C>A	XP_011525144.1:p.Ala883=
XM_011526843.1:c.1965C>A	XP_011525145.1:p.Ala655=
XM_011526844.1:c.1965C>A	XP_011525146.1:p.Ala655=
XM_011526840.2:c.3210C>A	XP_011525142.1:p.Ala1070=
XM_011526841.2:c.2796C>A	XP_011525143.1:p.Ala932=
XM_011526844.2:c.1965C>A	XP_011525146.1:p.Ala655=
XM_017026665.1:c.4218C>A	XP_016882154.1:p.Ala1406=
NM_001083961.2:c.4218C>A MANE Select	NP_001077430.1:p.Ala1406=
NM_173636.5:c.4203C>A	NP_775907.4:p.Ala1401=