Canonical Allele Identifier: CA405451689

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593679A>C (hg19) ; chr19:g.36102777A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102777A>C , CM000681.2:g.36102777A>C	GRCh38
NC_000019.9:g.36593679A>C , CM000681.1:g.36593679A>C	GRCh37
NC_000019.8:g.41285519A>C	NCBI36
NG_028101.1:g.52897A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3246A>C	ENSP00000270301.6:p.Glu1082Asp
ENST00000401500.7:c.3261A>C MANE Select	ENSP00000384792.1:p.Glu1087Asp
ENST00000587391.6:c.*3121A>C	ENSP00000465525.1:n.*3121A>C
ENST00000679357.1:c.1341A>C
ENST00000679598.1:c.26A>C
ENST00000679682.1:c.3246A>C	ENSP00000506226.1:p.Glu1082Asp
ENST00000679714.1:c.3255A>C	ENSP00000506627.1:p.Glu1085Asp
ENST00000679757.1:c.2910A>C	ENSP00000505158.1:p.Glu970Asp
ENST00000679858.1:c.*2643A>C	ENSP00000505655.1:n.*2643A>C
ENST00000680211.1:c.-139A>C	ENSP00000506102.1:n.-139A>C
ENST00000680280.1:n.548A>C
ENST00000680349.1:n.1829A>C
ENST00000680403.1:c.3246A>C	ENSP00000505677.1:p.Glu1082Asp
ENST00000680564.1:c.3012A>C	ENSP00000505582.1:p.Glu1004Asp
ENST00000680590.1:c.*1641A>C	ENSP00000505350.1:n.*1641A>C
ENST00000680597.1:c.26A>C
ENST00000680739.1:c.276A>C
ENST00000680773.1:n.1762A>C
ENST00000680806.1:c.*2564A>C	ENSP00000506418.1:n.*2564A>C
ENST00000680997.1:n.1193A>C
ENST00000681608.1:n.794A>C
ENST00000681625.1:c.*593A>C	ENSP00000505555.1:n.*593A>C
ENST00000681648.1:n.560A>C
ENST00000270301.11:c.3246A>C	ENSP00000270301.6:p.Glu1082Asp
ENST00000401500.6:c.3261A>C	ENSP00000384792.1:p.Glu1087Asp
ENST00000587391.5:c.*3121A>C	ENSP00000465525.1:n.*3121A>C
NM_001083961.1:c.3261A>C	NP_001077430.1:p.Glu1087Asp
NM_173636.4:c.3246A>C	NP_775907.4:p.Glu1082Asp
XM_005258809.2:c.3150A>C	XP_005258866.1:p.Glu1050Asp
XM_011526837.1:c.3246A>C	XP_011525139.1:p.Glu1082Asp
XM_011526838.1:c.3012A>C	XP_011525140.1:p.Glu1004Asp
XM_011526839.1:c.2910A>C	XP_011525141.1:p.Glu970Asp
XM_011526840.1:c.2253A>C	XP_011525142.1:p.Glu751Asp
XM_011526841.1:c.1839A>C	XP_011525143.1:p.Glu613Asp
XM_011526842.1:c.1692A>C	XP_011525144.1:p.Glu564Asp
XM_011526843.1:c.1008A>C	XP_011525145.1:p.Glu336Asp
XM_011526844.1:c.1008A>C	XP_011525146.1:p.Glu336Asp
XM_011526840.2:c.2253A>C	XP_011525142.1:p.Glu751Asp
XM_011526841.2:c.1839A>C	XP_011525143.1:p.Glu613Asp
XM_011526844.2:c.1008A>C	XP_011525146.1:p.Glu336Asp
XM_017026665.1:c.3261A>C	XP_016882154.1:p.Glu1087Asp
NM_001083961.2:c.3261A>C MANE Select	NP_001077430.1:p.Glu1087Asp
NM_173636.5:c.3246A>C	NP_775907.4:p.Glu1082Asp