Canonical Allele Identifier: CA405460875

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595501T>A (hg19) ; chr19:g.36104599T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104599T>A , CM000681.2:g.36104599T>A	GRCh38
NC_000019.9:g.36595501T>A , CM000681.1:g.36595501T>A	GRCh37
NC_000019.8:g.41287341T>A	NCBI36
NG_028101.1:g.54719T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4220T>A	ENSP00000270301.6:p.Leu1407His
ENST00000401500.7:c.4235T>A MANE Select	ENSP00000384792.1:p.Leu1412His
ENST00000587391.6:c.*4095T>A	ENSP00000465525.1:n.*4095T>A
ENST00000679357.1:c.2315T>A
ENST00000679598.1:c.980T>A
ENST00000679682.1:c.4220T>A	ENSP00000506226.1:p.Leu1407His
ENST00000679714.1:c.4229T>A	ENSP00000506627.1:p.Leu1410His
ENST00000679757.1:c.3884T>A	ENSP00000505158.1:p.Leu1295His
ENST00000679858.1:c.*3617T>A	ENSP00000505655.1:n.*3617T>A
ENST00000680211.1:c.836T>A	ENSP00000506102.1:p.Leu279His
ENST00000680280.1:n.1738T>A
ENST00000680349.1:n.2884T>A
ENST00000680403.1:c.4220T>A	ENSP00000505677.1:p.Leu1407His
ENST00000680564.1:c.3986T>A	ENSP00000505582.1:p.Leu1329His
ENST00000680590.1:c.*2615T>A	ENSP00000505350.1:n.*2615T>A
ENST00000680597.1:c.968T>A
ENST00000680739.1:c.1250T>A
ENST00000680773.1:n.2736T>A
ENST00000680806.1:c.*3538T>A	ENSP00000506418.1:n.*3538T>A
ENST00000680997.1:n.2167T>A
ENST00000681608.1:n.2080T>A
ENST00000681625.1:c.*1567T>A	ENSP00000505555.1:n.*1567T>A
ENST00000681648.1:n.2286T>A
ENST00000270301.11:c.4220T>A	ENSP00000270301.6:p.Leu1407His
ENST00000401500.6:c.4235T>A	ENSP00000384792.1:p.Leu1412His
ENST00000587391.5:c.*4095T>A	ENSP00000465525.1:n.*4095T>A
NM_001083961.1:c.4235T>A	NP_001077430.1:p.Leu1412His
NM_173636.4:c.4220T>A	NP_775907.4:p.Leu1407His
XM_005258809.2:c.4124T>A	XP_005258866.1:p.Leu1375His
XM_011526837.1:c.4220T>A	XP_011525139.1:p.Leu1407His
XM_011526838.1:c.3986T>A	XP_011525140.1:p.Leu1329His
XM_011526839.1:c.3884T>A	XP_011525141.1:p.Leu1295His
XM_011526840.1:c.3227T>A	XP_011525142.1:p.Leu1076His
XM_011526841.1:c.2813T>A	XP_011525143.1:p.Leu938His
XM_011526842.1:c.2666T>A	XP_011525144.1:p.Leu889His
XM_011526843.1:c.1982T>A	XP_011525145.1:p.Leu661His
XM_011526844.1:c.1982T>A	XP_011525146.1:p.Leu661His
XM_011526840.2:c.3227T>A	XP_011525142.1:p.Leu1076His
XM_011526841.2:c.2813T>A	XP_011525143.1:p.Leu938His
XM_011526844.2:c.1982T>A	XP_011525146.1:p.Leu661His
XM_017026665.1:c.4235T>A	XP_016882154.1:p.Leu1412His
NM_001083961.2:c.4235T>A MANE Select	NP_001077430.1:p.Leu1412His
NM_173636.5:c.4220T>A	NP_775907.4:p.Leu1407His