Canonical Allele Identifier: CA405451669

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593677G>C (hg19) ; chr19:g.36102775G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102775G>C , CM000681.2:g.36102775G>C	GRCh38
NC_000019.9:g.36593677G>C , CM000681.1:g.36593677G>C	GRCh37
NC_000019.8:g.41285517G>C	NCBI36
NG_028101.1:g.52895G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3244G>C	ENSP00000270301.6:p.Glu1082Gln
ENST00000401500.7:c.3259G>C MANE Select	ENSP00000384792.1:p.Glu1087Gln
ENST00000587391.6:c.*3119G>C	ENSP00000465525.1:n.*3119G>C
ENST00000679357.1:c.1339G>C
ENST00000679598.1:c.24G>C
ENST00000679682.1:c.3244G>C	ENSP00000506226.1:p.Glu1082Gln
ENST00000679714.1:c.3253G>C	ENSP00000506627.1:p.Glu1085Gln
ENST00000679757.1:c.2908G>C	ENSP00000505158.1:p.Glu970Gln
ENST00000679858.1:c.*2641G>C	ENSP00000505655.1:n.*2641G>C
ENST00000680211.1:c.-141G>C	ENSP00000506102.1:n.-141G>C
ENST00000680280.1:n.546G>C
ENST00000680349.1:n.1827G>C
ENST00000680403.1:c.3244G>C	ENSP00000505677.1:p.Glu1082Gln
ENST00000680564.1:c.3010G>C	ENSP00000505582.1:p.Glu1004Gln
ENST00000680590.1:c.*1639G>C	ENSP00000505350.1:n.*1639G>C
ENST00000680597.1:c.24G>C
ENST00000680739.1:c.274G>C
ENST00000680773.1:n.1760G>C
ENST00000680806.1:c.*2562G>C	ENSP00000506418.1:n.*2562G>C
ENST00000680997.1:n.1191G>C
ENST00000681608.1:n.792G>C
ENST00000681625.1:c.*591G>C	ENSP00000505555.1:n.*591G>C
ENST00000681648.1:n.558G>C
ENST00000270301.11:c.3244G>C	ENSP00000270301.6:p.Glu1082Gln
ENST00000401500.6:c.3259G>C	ENSP00000384792.1:p.Glu1087Gln
ENST00000587391.5:c.*3119G>C	ENSP00000465525.1:n.*3119G>C
NM_001083961.1:c.3259G>C	NP_001077430.1:p.Glu1087Gln
NM_173636.4:c.3244G>C	NP_775907.4:p.Glu1082Gln
XM_005258809.2:c.3148G>C	XP_005258866.1:p.Glu1050Gln
XM_011526837.1:c.3244G>C	XP_011525139.1:p.Glu1082Gln
XM_011526838.1:c.3010G>C	XP_011525140.1:p.Glu1004Gln
XM_011526839.1:c.2908G>C	XP_011525141.1:p.Glu970Gln
XM_011526840.1:c.2251G>C	XP_011525142.1:p.Glu751Gln
XM_011526841.1:c.1837G>C	XP_011525143.1:p.Glu613Gln
XM_011526842.1:c.1690G>C	XP_011525144.1:p.Glu564Gln
XM_011526843.1:c.1006G>C	XP_011525145.1:p.Glu336Gln
XM_011526844.1:c.1006G>C	XP_011525146.1:p.Glu336Gln
XM_011526840.2:c.2251G>C	XP_011525142.1:p.Glu751Gln
XM_011526841.2:c.1837G>C	XP_011525143.1:p.Glu613Gln
XM_011526844.2:c.1006G>C	XP_011525146.1:p.Glu336Gln
XM_017026665.1:c.3259G>C	XP_016882154.1:p.Glu1087Gln
NM_001083961.2:c.3259G>C MANE Select	NP_001077430.1:p.Glu1087Gln
NM_173636.5:c.3244G>C	NP_775907.4:p.Glu1082Gln