Canonical Allele Identifier: CA405451809

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593688C>G (hg19) ; chr19:g.36102786C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102786C>G , CM000681.2:g.36102786C>G	GRCh38
NC_000019.9:g.36593688C>G , CM000681.1:g.36593688C>G	GRCh37
NC_000019.8:g.41285528C>G	NCBI36
NG_028101.1:g.52906C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3255C>G	ENSP00000270301.6:p.Asp1085Glu
ENST00000401500.7:c.3270C>G MANE Select	ENSP00000384792.1:p.Asp1090Glu
ENST00000587391.6:c.*3130C>G	ENSP00000465525.1:n.*3130C>G
ENST00000679357.1:c.1350C>G
ENST00000679598.1:c.35C>G
ENST00000679682.1:c.3255C>G	ENSP00000506226.1:p.Asp1085Glu
ENST00000679714.1:c.3264C>G	ENSP00000506627.1:p.Asp1088Glu
ENST00000679757.1:c.2919C>G	ENSP00000505158.1:p.Asp973Glu
ENST00000679858.1:c.*2652C>G	ENSP00000505655.1:n.*2652C>G
ENST00000680211.1:c.-130C>G	ENSP00000506102.1:n.-130C>G
ENST00000680280.1:n.557C>G
ENST00000680349.1:n.1838C>G
ENST00000680403.1:c.3255C>G	ENSP00000505677.1:p.Asp1085Glu
ENST00000680564.1:c.3021C>G	ENSP00000505582.1:p.Asp1007Glu
ENST00000680590.1:c.*1650C>G	ENSP00000505350.1:n.*1650C>G
ENST00000680597.1:c.35C>G
ENST00000680739.1:c.285C>G
ENST00000680773.1:n.1771C>G
ENST00000680806.1:c.*2573C>G	ENSP00000506418.1:n.*2573C>G
ENST00000680997.1:n.1202C>G
ENST00000681608.1:n.803C>G
ENST00000681625.1:c.*602C>G	ENSP00000505555.1:n.*602C>G
ENST00000681648.1:n.569C>G
ENST00000270301.11:c.3255C>G	ENSP00000270301.6:p.Asp1085Glu
ENST00000401500.6:c.3270C>G	ENSP00000384792.1:p.Asp1090Glu
ENST00000587391.5:c.*3130C>G	ENSP00000465525.1:n.*3130C>G
NM_001083961.1:c.3270C>G	NP_001077430.1:p.Asp1090Glu
NM_173636.4:c.3255C>G	NP_775907.4:p.Asp1085Glu
XM_005258809.2:c.3159C>G	XP_005258866.1:p.Asp1053Glu
XM_011526837.1:c.3255C>G	XP_011525139.1:p.Asp1085Glu
XM_011526838.1:c.3021C>G	XP_011525140.1:p.Asp1007Glu
XM_011526839.1:c.2919C>G	XP_011525141.1:p.Asp973Glu
XM_011526840.1:c.2262C>G	XP_011525142.1:p.Asp754Glu
XM_011526841.1:c.1848C>G	XP_011525143.1:p.Asp616Glu
XM_011526842.1:c.1701C>G	XP_011525144.1:p.Asp567Glu
XM_011526843.1:c.1017C>G	XP_011525145.1:p.Asp339Glu
XM_011526844.1:c.1017C>G	XP_011525146.1:p.Asp339Glu
XM_011526840.2:c.2262C>G	XP_011525142.1:p.Asp754Glu
XM_011526841.2:c.1848C>G	XP_011525143.1:p.Asp616Glu
XM_011526844.2:c.1017C>G	XP_011525146.1:p.Asp339Glu
XM_017026665.1:c.3270C>G	XP_016882154.1:p.Asp1090Glu
NM_001083961.2:c.3270C>G MANE Select	NP_001077430.1:p.Asp1090Glu
NM_173636.5:c.3255C>G	NP_775907.4:p.Asp1085Glu