Canonical Allele Identifier: CA507318432

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595427T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104525T>A , CM000681.2:g.36104525T>A	GRCh38
NC_000019.9:g.36595427T>A , CM000681.1:g.36595427T>A	GRCh37
NC_000019.8:g.41287267T>A	NCBI36
NG_028101.1:g.54645T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4146T>A	ENSP00000270301.6:p.Leu1382=
ENST00000401500.7:c.4161T>A MANE Select	ENSP00000384792.1:p.Leu1387=
ENST00000587391.6:c.*4021T>A	ENSP00000465525.1:n.*4021T>A
ENST00000679357.1:c.2241T>A
ENST00000679598.1:c.919-13T>A
ENST00000679682.1:c.4146T>A	ENSP00000506226.1:p.Leu1382=
ENST00000679714.1:c.4155T>A	ENSP00000506627.1:p.Leu1385=
ENST00000679757.1:c.3810T>A	ENSP00000505158.1:p.Leu1270=
ENST00000679858.1:c.*3543T>A	ENSP00000505655.1:n.*3543T>A
ENST00000680211.1:c.762T>A	ENSP00000506102.1:p.Leu254=
ENST00000680280.1:n.1664T>A
ENST00000680349.1:n.2810T>A
ENST00000680403.1:c.4146T>A	ENSP00000505677.1:p.Leu1382=
ENST00000680564.1:c.3912T>A	ENSP00000505582.1:p.Leu1304=
ENST00000680590.1:c.*2541T>A	ENSP00000505350.1:n.*2541T>A
ENST00000680597.1:c.894T>A
ENST00000680739.1:c.1176T>A
ENST00000680773.1:n.2662T>A
ENST00000680806.1:c.*3464T>A	ENSP00000506418.1:n.*3464T>A
ENST00000680997.1:n.2093T>A
ENST00000681608.1:n.2006T>A
ENST00000681625.1:c.*1493T>A	ENSP00000505555.1:n.*1493T>A
ENST00000681648.1:n.2212T>A
ENST00000270301.11:c.4146T>A	ENSP00000270301.6:p.Leu1382=
ENST00000401500.6:c.4161T>A	ENSP00000384792.1:p.Leu1387=
ENST00000587391.5:c.*4021T>A	ENSP00000465525.1:n.*4021T>A
NM_001083961.1:c.4161T>A	NP_001077430.1:p.Leu1387=
NM_173636.4:c.4146T>A	NP_775907.4:p.Leu1382=
XM_005258809.2:c.4050T>A	XP_005258866.1:p.Leu1350=
XM_011526837.1:c.4146T>A	XP_011525139.1:p.Leu1382=
XM_011526838.1:c.3912T>A	XP_011525140.1:p.Leu1304=
XM_011526839.1:c.3810T>A	XP_011525141.1:p.Leu1270=
XM_011526840.1:c.3153T>A	XP_011525142.1:p.Leu1051=
XM_011526841.1:c.2739T>A	XP_011525143.1:p.Leu913=
XM_011526842.1:c.2592T>A	XP_011525144.1:p.Leu864=
XM_011526843.1:c.1908T>A	XP_011525145.1:p.Leu636=
XM_011526844.1:c.1908T>A	XP_011525146.1:p.Leu636=
XM_011526840.2:c.3153T>A	XP_011525142.1:p.Leu1051=
XM_011526841.2:c.2739T>A	XP_011525143.1:p.Leu913=
XM_011526844.2:c.1908T>A	XP_011525146.1:p.Leu636=
XM_017026665.1:c.4161T>A	XP_016882154.1:p.Leu1387=
NM_001083961.2:c.4161T>A MANE Select	NP_001077430.1:p.Leu1387=
NM_173636.5:c.4146T>A	NP_775907.4:p.Leu1382=