Canonical Allele Identifier: CA1139666416

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36090449dup , CM000681.2:g.36090449dup	GRCh38
NC_000019.9:g.36581351dup , CM000681.1:g.36581351dup	GRCh37
NC_000019.8:g.41273191dup	NCBI36
NG_028101.1:g.40569dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.1963dup	ENSP00000270301.6:p.Tyr655LeufsTer18
ENST00000401500.7:c.1963dup MANE Select	ENSP00000384792.1:p.Tyr655LeufsTer18
ENST00000587391.6:c.*653dup	ENSP00000465525.1:n.*653dup
ENST00000679489.1:c.281dup
ENST00000679682.1:c.1948dup	ENSP00000506226.1:p.Tyr650LeufsTer18
ENST00000679714.1:c.1957dup	ENSP00000506627.1:p.Tyr653LeufsTer18
ENST00000679757.1:c.1612dup	ENSP00000505158.1:p.Tyr538LeufsTer18
ENST00000679858.1:c.*760dup	ENSP00000505655.1:n.*760dup
ENST00000680377.1:c.413dup
ENST00000680403.1:c.1963dup	ENSP00000505677.1:p.Tyr655LeufsTer18
ENST00000680489.1:n.2286dup
ENST00000680564.1:c.1963dup	ENSP00000505582.1:p.Tyr655LeufsTer18
ENST00000680590.1:c.*362dup	ENSP00000505350.1:n.*362dup
ENST00000680806.1:c.*792dup	ENSP00000506418.1:n.*792dup
ENST00000680858.1:c.408+1143dup
ENST00000681302.1:c.413dup
ENST00000681625.1:c.1948dup	ENSP00000505555.1:p.Tyr650LeufsTer18
ENST00000270301.11:c.1963dup	ENSP00000270301.6:p.Tyr655LeufsTer18
ENST00000401500.6:c.1963dup	ENSP00000384792.1:p.Tyr655LeufsTer18
ENST00000587391.5:c.*653dup	ENSP00000465525.1:n.*653dup
NM_001083961.1:c.1963dup	NP_001077430.1:p.Tyr655LeufsTer18
NM_173636.4:c.1963dup	NP_775907.4:p.Tyr655LeufsTer18
XM_005258809.2:c.1963dup	XP_005258866.1:p.Tyr655LeufsTer18
XM_011526837.1:c.1948dup	XP_011525139.1:p.Tyr650LeufsTer18
XM_011526838.1:c.1963dup	XP_011525140.1:p.Tyr655LeufsTer18
XM_011526839.1:c.1612dup	XP_011525141.1:p.Tyr538LeufsTer18
XM_011526840.1:c.955dup	XP_011525142.1:p.Tyr319LeufsTer18
XM_011526841.1:c.541dup	XP_011525143.1:p.Tyr181LeufsTer18
XM_011526842.1:c.394dup	XP_011525144.1:p.Tyr132LeufsTer18
XM_011526843.1:c.-115dup	XP_011525145.1:n.-115dup
XM_011526840.2:c.955dup	XP_011525142.1:p.Tyr319LeufsTer18
XM_011526841.2:c.541dup	XP_011525143.1:p.Tyr181LeufsTer18
XM_017026665.1:c.1963dup	XP_016882154.1:p.Tyr655LeufsTer18
XR_001753671.1:n.2054dup
XR_001753672.1:n.2054dup
NM_001083961.2:c.1963dup MANE Select	NP_001077430.1:p.Tyr655LeufsTer18
NM_173636.5:c.1963dup	NP_775907.4:p.Tyr655LeufsTer18