Canonical Allele Identifier: CA405450062

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592945T>A (hg19) ; chr19:g.36102043T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102043T>A , CM000681.2:g.36102043T>A	GRCh38
NC_000019.9:g.36592945T>A , CM000681.1:g.36592945T>A	GRCh37
NC_000019.8:g.41284785T>A	NCBI36
NG_028101.1:g.52163T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3112T>A	ENSP00000270301.6:p.Ser1038Thr
ENST00000401500.7:c.3112T>A MANE Select	ENSP00000384792.1:p.Ser1038Thr
ENST00000587391.6:c.*2387T>A	ENSP00000465525.1:n.*2387T>A
ENST00000679357.1:c.902T>A
ENST00000679422.1:c.791T>A
ENST00000679682.1:c.3097T>A	ENSP00000506226.1:p.Ser1033Thr
ENST00000679714.1:c.3106T>A	ENSP00000506627.1:p.Ser1036Thr
ENST00000679757.1:c.2761T>A	ENSP00000505158.1:p.Ser921Thr
ENST00000679858.1:c.*2494T>A	ENSP00000505655.1:n.*2494T>A
ENST00000680211.1:c.-288T>A	ENSP00000506102.1:n.-288T>A
ENST00000680349.1:n.1095T>A
ENST00000680403.1:c.3112T>A	ENSP00000505677.1:p.Ser1038Thr
ENST00000680564.1:c.2972-694T>A	ENSP00000505582.1:n.2972-694T>A
ENST00000680590.1:c.*1507T>A	ENSP00000505350.1:n.*1507T>A
ENST00000680739.1:c.30T>A
ENST00000680773.1:n.1028T>A
ENST00000680806.1:c.*1830T>A	ENSP00000506418.1:n.*1830T>A
ENST00000680997.1:n.459T>A
ENST00000681088.1:c.774T>A
ENST00000681608.1:n.60T>A
ENST00000681625.1:c.*444T>A	ENSP00000505555.1:n.*444T>A
ENST00000270301.11:c.3112T>A	ENSP00000270301.6:p.Ser1038Thr
ENST00000401500.6:c.3112T>A	ENSP00000384792.1:p.Ser1038Thr
ENST00000587391.5:c.*2387T>A	ENSP00000465525.1:n.*2387T>A
NM_001083961.1:c.3112T>A	NP_001077430.1:p.Ser1038Thr
NM_173636.4:c.3112T>A	NP_775907.4:p.Ser1038Thr
XM_005258809.2:c.3001T>A	XP_005258866.1:p.Ser1001Thr
XM_011526837.1:c.3097T>A	XP_011525139.1:p.Ser1033Thr
XM_011526838.1:c.2972-694T>A	XP_011525140.1:n.2972-694T>A
XM_011526839.1:c.2761T>A	XP_011525141.1:p.Ser921Thr
XM_011526840.1:c.2104T>A	XP_011525142.1:p.Ser702Thr
XM_011526841.1:c.1690T>A	XP_011525143.1:p.Ser564Thr
XM_011526842.1:c.1543T>A	XP_011525144.1:p.Ser515Thr
XM_011526843.1:c.859T>A	XP_011525145.1:p.Ser287Thr
XM_011526844.1:c.859T>A	XP_011525146.1:p.Ser287Thr
XM_011526840.2:c.2104T>A	XP_011525142.1:p.Ser702Thr
XM_011526841.2:c.1690T>A	XP_011525143.1:p.Ser564Thr
XM_011526844.2:c.859T>A	XP_011525146.1:p.Ser287Thr
XM_017026665.1:c.3112T>A	XP_016882154.1:p.Ser1038Thr
NM_001083961.2:c.3112T>A MANE Select	NP_001077430.1:p.Ser1038Thr
NM_173636.5:c.3112T>A	NP_775907.4:p.Ser1038Thr