Canonical Allele Identifier: CA507318601

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595487G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104585G>T , CM000681.2:g.36104585G>T	GRCh38
NC_000019.9:g.36595487G>T , CM000681.1:g.36595487G>T	GRCh37
NC_000019.8:g.41287327G>T	NCBI36
NG_028101.1:g.54705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4206G>T	ENSP00000270301.6:p.Leu1402=
ENST00000401500.7:c.4221G>T MANE Select	ENSP00000384792.1:p.Leu1407=
ENST00000587391.6:c.*4081G>T	ENSP00000465525.1:n.*4081G>T
ENST00000679357.1:c.2301G>T
ENST00000679598.1:c.966G>T
ENST00000679682.1:c.4206G>T	ENSP00000506226.1:p.Leu1402=
ENST00000679714.1:c.4215G>T	ENSP00000506627.1:p.Leu1405=
ENST00000679757.1:c.3870G>T	ENSP00000505158.1:p.Leu1290=
ENST00000679858.1:c.*3603G>T	ENSP00000505655.1:n.*3603G>T
ENST00000680211.1:c.822G>T	ENSP00000506102.1:p.Leu274=
ENST00000680280.1:n.1724G>T
ENST00000680349.1:n.2870G>T
ENST00000680403.1:c.4206G>T	ENSP00000505677.1:p.Leu1402=
ENST00000680564.1:c.3972G>T	ENSP00000505582.1:p.Leu1324=
ENST00000680590.1:c.*2601G>T	ENSP00000505350.1:n.*2601G>T
ENST00000680597.1:c.954G>T
ENST00000680739.1:c.1236G>T
ENST00000680773.1:n.2722G>T
ENST00000680806.1:c.*3524G>T	ENSP00000506418.1:n.*3524G>T
ENST00000680997.1:n.2153G>T
ENST00000681608.1:n.2066G>T
ENST00000681625.1:c.*1553G>T	ENSP00000505555.1:n.*1553G>T
ENST00000681648.1:n.2272G>T
ENST00000270301.11:c.4206G>T	ENSP00000270301.6:p.Leu1402=
ENST00000401500.6:c.4221G>T	ENSP00000384792.1:p.Leu1407=
ENST00000587391.5:c.*4081G>T	ENSP00000465525.1:n.*4081G>T
NM_001083961.1:c.4221G>T	NP_001077430.1:p.Leu1407=
NM_173636.4:c.4206G>T	NP_775907.4:p.Leu1402=
XM_005258809.2:c.4110G>T	XP_005258866.1:p.Leu1370=
XM_011526837.1:c.4206G>T	XP_011525139.1:p.Leu1402=
XM_011526838.1:c.3972G>T	XP_011525140.1:p.Leu1324=
XM_011526839.1:c.3870G>T	XP_011525141.1:p.Leu1290=
XM_011526840.1:c.3213G>T	XP_011525142.1:p.Leu1071=
XM_011526841.1:c.2799G>T	XP_011525143.1:p.Leu933=
XM_011526842.1:c.2652G>T	XP_011525144.1:p.Leu884=
XM_011526843.1:c.1968G>T	XP_011525145.1:p.Leu656=
XM_011526844.1:c.1968G>T	XP_011525146.1:p.Leu656=
XM_011526840.2:c.3213G>T	XP_011525142.1:p.Leu1071=
XM_011526841.2:c.2799G>T	XP_011525143.1:p.Leu933=
XM_011526844.2:c.1968G>T	XP_011525146.1:p.Leu656=
XM_017026665.1:c.4221G>T	XP_016882154.1:p.Leu1407=
NM_001083961.2:c.4221G>T MANE Select	NP_001077430.1:p.Leu1407=
NM_173636.5:c.4206G>T	NP_775907.4:p.Leu1402=