Canonical Allele Identifier: CA405450161

Gene: WDR62

Linked Data

• dbSNP Id: rs1973383823
• MyVariant Identifiers: chr19:g.36592960C>A (hg19) ; chr19:g.36102058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102058C>A , CM000681.2:g.36102058C>A	GRCh38
NC_000019.9:g.36592960C>A , CM000681.1:g.36592960C>A	GRCh37
NC_000019.8:g.41284800C>A	NCBI36
NG_028101.1:g.52178C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3127C>A	ENSP00000270301.6:p.Pro1043Thr
ENST00000401500.7:c.3127C>A MANE Select	ENSP00000384792.1:p.Pro1043Thr
ENST00000587391.6:c.*2402C>A	ENSP00000465525.1:n.*2402C>A
ENST00000679357.1:c.917C>A
ENST00000679422.1:c.806C>A
ENST00000679682.1:c.3112C>A	ENSP00000506226.1:p.Pro1038Thr
ENST00000679714.1:c.3121C>A	ENSP00000506627.1:p.Pro1041Thr
ENST00000679757.1:c.2776C>A	ENSP00000505158.1:p.Pro926Thr
ENST00000679858.1:c.*2509C>A	ENSP00000505655.1:n.*2509C>A
ENST00000680211.1:c.-273C>A	ENSP00000506102.1:n.-273C>A
ENST00000680349.1:n.1110C>A
ENST00000680403.1:c.3127C>A	ENSP00000505677.1:p.Pro1043Thr
ENST00000680564.1:c.2972-679C>A	ENSP00000505582.1:n.2972-679C>A
ENST00000680590.1:c.*1522C>A	ENSP00000505350.1:n.*1522C>A
ENST00000680739.1:c.45C>A
ENST00000680773.1:n.1043C>A
ENST00000680806.1:c.*1845C>A	ENSP00000506418.1:n.*1845C>A
ENST00000680997.1:n.474C>A
ENST00000681088.1:c.789C>A
ENST00000681608.1:n.75C>A
ENST00000681625.1:c.*459C>A	ENSP00000505555.1:n.*459C>A
ENST00000270301.11:c.3127C>A	ENSP00000270301.6:p.Pro1043Thr
ENST00000401500.6:c.3127C>A	ENSP00000384792.1:p.Pro1043Thr
ENST00000587391.5:c.*2402C>A	ENSP00000465525.1:n.*2402C>A
NM_001083961.1:c.3127C>A	NP_001077430.1:p.Pro1043Thr
NM_173636.4:c.3127C>A	NP_775907.4:p.Pro1043Thr
XM_005258809.2:c.3016C>A	XP_005258866.1:p.Pro1006Thr
XM_011526837.1:c.3112C>A	XP_011525139.1:p.Pro1038Thr
XM_011526838.1:c.2972-679C>A	XP_011525140.1:n.2972-679C>A
XM_011526839.1:c.2776C>A	XP_011525141.1:p.Pro926Thr
XM_011526840.1:c.2119C>A	XP_011525142.1:p.Pro707Thr
XM_011526841.1:c.1705C>A	XP_011525143.1:p.Pro569Thr
XM_011526842.1:c.1558C>A	XP_011525144.1:p.Pro520Thr
XM_011526843.1:c.874C>A	XP_011525145.1:p.Pro292Thr
XM_011526844.1:c.874C>A	XP_011525146.1:p.Pro292Thr
XM_011526840.2:c.2119C>A	XP_011525142.1:p.Pro707Thr
XM_011526841.2:c.1705C>A	XP_011525143.1:p.Pro569Thr
XM_011526844.2:c.874C>A	XP_011525146.1:p.Pro292Thr
XM_017026665.1:c.3127C>A	XP_016882154.1:p.Pro1043Thr
NM_001083961.2:c.3127C>A MANE Select	NP_001077430.1:p.Pro1043Thr
NM_173636.5:c.3127C>A	NP_775907.4:p.Pro1043Thr