Canonical Allele Identifier: CA405451581

Gene: WDR62

Linked Data

• dbSNP Id: rs1287480501
• gnomAD v2: 19-36593668-G-C
• gnomAD v4: 19-36102766-G-C
• MyVariant Identifiers: chr19:g.36593668G>C (hg19) ; chr19:g.36102766G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102766G>C , CM000681.2:g.36102766G>C	GRCh38
NC_000019.9:g.36593668G>C , CM000681.1:g.36593668G>C	GRCh37
NC_000019.8:g.41285508G>C	NCBI36
NG_028101.1:g.52886G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3235G>C	ENSP00000270301.6:p.Glu1079Gln
ENST00000401500.7:c.3250G>C MANE Select	ENSP00000384792.1:p.Glu1084Gln
ENST00000587391.6:c.*3110G>C	ENSP00000465525.1:n.*3110G>C
ENST00000679357.1:c.1330G>C
ENST00000679598.1:c.15G>C
ENST00000679682.1:c.3235G>C	ENSP00000506226.1:p.Glu1079Gln
ENST00000679714.1:c.3244G>C	ENSP00000506627.1:p.Glu1082Gln
ENST00000679757.1:c.2899G>C	ENSP00000505158.1:p.Glu967Gln
ENST00000679858.1:c.*2632G>C	ENSP00000505655.1:n.*2632G>C
ENST00000680211.1:c.-150G>C	ENSP00000506102.1:n.-150G>C
ENST00000680280.1:n.537G>C
ENST00000680349.1:n.1818G>C
ENST00000680403.1:c.3235G>C	ENSP00000505677.1:p.Glu1079Gln
ENST00000680564.1:c.3001G>C	ENSP00000505582.1:p.Glu1001Gln
ENST00000680590.1:c.*1630G>C	ENSP00000505350.1:n.*1630G>C
ENST00000680597.1:c.15G>C
ENST00000680739.1:c.265G>C
ENST00000680773.1:n.1751G>C
ENST00000680806.1:c.*2553G>C	ENSP00000506418.1:n.*2553G>C
ENST00000680997.1:n.1182G>C
ENST00000681608.1:n.783G>C
ENST00000681625.1:c.*582G>C	ENSP00000505555.1:n.*582G>C
ENST00000681648.1:n.549G>C
ENST00000270301.11:c.3235G>C	ENSP00000270301.6:p.Glu1079Gln
ENST00000401500.6:c.3250G>C	ENSP00000384792.1:p.Glu1084Gln
ENST00000587391.5:c.*3110G>C	ENSP00000465525.1:n.*3110G>C
NM_001083961.1:c.3250G>C	NP_001077430.1:p.Glu1084Gln
NM_173636.4:c.3235G>C	NP_775907.4:p.Glu1079Gln
XM_005258809.2:c.3139G>C	XP_005258866.1:p.Glu1047Gln
XM_011526837.1:c.3235G>C	XP_011525139.1:p.Glu1079Gln
XM_011526838.1:c.3001G>C	XP_011525140.1:p.Glu1001Gln
XM_011526839.1:c.2899G>C	XP_011525141.1:p.Glu967Gln
XM_011526840.1:c.2242G>C	XP_011525142.1:p.Glu748Gln
XM_011526841.1:c.1828G>C	XP_011525143.1:p.Glu610Gln
XM_011526842.1:c.1681G>C	XP_011525144.1:p.Glu561Gln
XM_011526843.1:c.997G>C	XP_011525145.1:p.Glu333Gln
XM_011526844.1:c.997G>C	XP_011525146.1:p.Glu333Gln
XM_011526840.2:c.2242G>C	XP_011525142.1:p.Glu748Gln
XM_011526841.2:c.1828G>C	XP_011525143.1:p.Glu610Gln
XM_011526844.2:c.997G>C	XP_011525146.1:p.Glu333Gln
XM_017026665.1:c.3250G>C	XP_016882154.1:p.Glu1084Gln
NM_001083961.2:c.3250G>C MANE Select	NP_001077430.1:p.Glu1084Gln
NM_173636.5:c.3235G>C	NP_775907.4:p.Glu1079Gln