Canonical Allele Identifier: CA405450088

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592949T>A (hg19) ; chr19:g.36102047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102047T>A , CM000681.2:g.36102047T>A	GRCh38
NC_000019.9:g.36592949T>A , CM000681.1:g.36592949T>A	GRCh37
NC_000019.8:g.41284789T>A	NCBI36
NG_028101.1:g.52167T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3116T>A	ENSP00000270301.6:p.Leu1039Gln
ENST00000401500.7:c.3116T>A MANE Select	ENSP00000384792.1:p.Leu1039Gln
ENST00000587391.6:c.*2391T>A	ENSP00000465525.1:n.*2391T>A
ENST00000679357.1:c.906T>A
ENST00000679422.1:c.795T>A
ENST00000679682.1:c.3101T>A	ENSP00000506226.1:p.Leu1034Gln
ENST00000679714.1:c.3110T>A	ENSP00000506627.1:p.Leu1037Gln
ENST00000679757.1:c.2765T>A	ENSP00000505158.1:p.Leu922Gln
ENST00000679858.1:c.*2498T>A	ENSP00000505655.1:n.*2498T>A
ENST00000680211.1:c.-284T>A	ENSP00000506102.1:n.-284T>A
ENST00000680349.1:n.1099T>A
ENST00000680403.1:c.3116T>A	ENSP00000505677.1:p.Leu1039Gln
ENST00000680564.1:c.2972-690T>A	ENSP00000505582.1:n.2972-690T>A
ENST00000680590.1:c.*1511T>A	ENSP00000505350.1:n.*1511T>A
ENST00000680739.1:c.34T>A
ENST00000680773.1:n.1032T>A
ENST00000680806.1:c.*1834T>A	ENSP00000506418.1:n.*1834T>A
ENST00000680997.1:n.463T>A
ENST00000681088.1:c.778T>A
ENST00000681608.1:n.64T>A
ENST00000681625.1:c.*448T>A	ENSP00000505555.1:n.*448T>A
ENST00000270301.11:c.3116T>A	ENSP00000270301.6:p.Leu1039Gln
ENST00000401500.6:c.3116T>A	ENSP00000384792.1:p.Leu1039Gln
ENST00000587391.5:c.*2391T>A	ENSP00000465525.1:n.*2391T>A
NM_001083961.1:c.3116T>A	NP_001077430.1:p.Leu1039Gln
NM_173636.4:c.3116T>A	NP_775907.4:p.Leu1039Gln
XM_005258809.2:c.3005T>A	XP_005258866.1:p.Leu1002Gln
XM_011526837.1:c.3101T>A	XP_011525139.1:p.Leu1034Gln
XM_011526838.1:c.2972-690T>A	XP_011525140.1:n.2972-690T>A
XM_011526839.1:c.2765T>A	XP_011525141.1:p.Leu922Gln
XM_011526840.1:c.2108T>A	XP_011525142.1:p.Leu703Gln
XM_011526841.1:c.1694T>A	XP_011525143.1:p.Leu565Gln
XM_011526842.1:c.1547T>A	XP_011525144.1:p.Leu516Gln
XM_011526843.1:c.863T>A	XP_011525145.1:p.Leu288Gln
XM_011526844.1:c.863T>A	XP_011525146.1:p.Leu288Gln
XM_011526840.2:c.2108T>A	XP_011525142.1:p.Leu703Gln
XM_011526841.2:c.1694T>A	XP_011525143.1:p.Leu565Gln
XM_011526844.2:c.863T>A	XP_011525146.1:p.Leu288Gln
XM_017026665.1:c.3116T>A	XP_016882154.1:p.Leu1039Gln
NM_001083961.2:c.3116T>A MANE Select	NP_001077430.1:p.Leu1039Gln
NM_173636.5:c.3116T>A	NP_775907.4:p.Leu1039Gln