Canonical Allele Identifier: CA405450140

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592956G>T (hg19) ; chr19:g.36102054G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102054G>T , CM000681.2:g.36102054G>T	GRCh38
NC_000019.9:g.36592956G>T , CM000681.1:g.36592956G>T	GRCh37
NC_000019.8:g.41284796G>T	NCBI36
NG_028101.1:g.52174G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3123G>T	ENSP00000270301.6:p.Glu1041Asp
ENST00000401500.7:c.3123G>T MANE Select	ENSP00000384792.1:p.Glu1041Asp
ENST00000587391.6:c.*2398G>T	ENSP00000465525.1:n.*2398G>T
ENST00000679357.1:c.913G>T
ENST00000679422.1:c.802G>T
ENST00000679682.1:c.3108G>T	ENSP00000506226.1:p.Glu1036Asp
ENST00000679714.1:c.3117G>T	ENSP00000506627.1:p.Glu1039Asp
ENST00000679757.1:c.2772G>T	ENSP00000505158.1:p.Glu924Asp
ENST00000679858.1:c.*2505G>T	ENSP00000505655.1:n.*2505G>T
ENST00000680211.1:c.-277G>T	ENSP00000506102.1:n.-277G>T
ENST00000680349.1:n.1106G>T
ENST00000680403.1:c.3123G>T	ENSP00000505677.1:p.Glu1041Asp
ENST00000680564.1:c.2972-683G>T	ENSP00000505582.1:n.2972-683G>T
ENST00000680590.1:c.*1518G>T	ENSP00000505350.1:n.*1518G>T
ENST00000680739.1:c.41G>T
ENST00000680773.1:n.1039G>T
ENST00000680806.1:c.*1841G>T	ENSP00000506418.1:n.*1841G>T
ENST00000680997.1:n.470G>T
ENST00000681088.1:c.785G>T
ENST00000681608.1:n.71G>T
ENST00000681625.1:c.*455G>T	ENSP00000505555.1:n.*455G>T
ENST00000270301.11:c.3123G>T	ENSP00000270301.6:p.Glu1041Asp
ENST00000401500.6:c.3123G>T	ENSP00000384792.1:p.Glu1041Asp
ENST00000587391.5:c.*2398G>T	ENSP00000465525.1:n.*2398G>T
NM_001083961.1:c.3123G>T	NP_001077430.1:p.Glu1041Asp
NM_173636.4:c.3123G>T	NP_775907.4:p.Glu1041Asp
XM_005258809.2:c.3012G>T	XP_005258866.1:p.Glu1004Asp
XM_011526837.1:c.3108G>T	XP_011525139.1:p.Glu1036Asp
XM_011526838.1:c.2972-683G>T	XP_011525140.1:n.2972-683G>T
XM_011526839.1:c.2772G>T	XP_011525141.1:p.Glu924Asp
XM_011526840.1:c.2115G>T	XP_011525142.1:p.Glu705Asp
XM_011526841.1:c.1701G>T	XP_011525143.1:p.Glu567Asp
XM_011526842.1:c.1554G>T	XP_011525144.1:p.Glu518Asp
XM_011526843.1:c.870G>T	XP_011525145.1:p.Glu290Asp
XM_011526844.1:c.870G>T	XP_011525146.1:p.Glu290Asp
XM_011526840.2:c.2115G>T	XP_011525142.1:p.Glu705Asp
XM_011526841.2:c.1701G>T	XP_011525143.1:p.Glu567Asp
XM_011526844.2:c.870G>T	XP_011525146.1:p.Glu290Asp
XM_017026665.1:c.3123G>T	XP_016882154.1:p.Glu1041Asp
NM_001083961.2:c.3123G>T MANE Select	NP_001077430.1:p.Glu1041Asp
NM_173636.5:c.3123G>T	NP_775907.4:p.Glu1041Asp