Canonical Allele Identifier: CA2584644441

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102130-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102131dup , CM000681.2:g.36102131dup	GRCh38
NC_000019.9:g.36593033dup , CM000681.1:g.36593033dup	GRCh37
NC_000019.8:g.41284873dup	NCBI36
NG_028101.1:g.52251dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3200dup	ENSP00000270301.6:p.Thr1068AspfsTer2
ENST00000401500.7:c.3200dup MANE Select	ENSP00000384792.1:p.Thr1068AspfsTer2
ENST00000587391.6:c.*2475dup	ENSP00000465525.1:n.*2475dup
ENST00000679357.1:c.990dup
ENST00000679422.1:c.879dup
ENST00000679682.1:c.3185dup	ENSP00000506226.1:p.Thr1063AspfsTer2
ENST00000679714.1:c.3194dup	ENSP00000506627.1:p.Thr1066AspfsTer2
ENST00000679757.1:c.2849dup	ENSP00000505158.1:p.Thr951AspfsTer2
ENST00000679858.1:c.*2582dup	ENSP00000505655.1:n.*2582dup
ENST00000680211.1:c.-200dup	ENSP00000506102.1:n.-200dup
ENST00000680349.1:n.1183dup
ENST00000680403.1:c.3200dup	ENSP00000505677.1:p.Thr1068AspfsTer2
ENST00000680564.1:c.2972-606dup	ENSP00000505582.1:n.2972-606dup
ENST00000680590.1:c.*1595dup	ENSP00000505350.1:n.*1595dup
ENST00000680739.1:c.118dup
ENST00000680773.1:n.1116dup
ENST00000680806.1:c.*1918dup	ENSP00000506418.1:n.*1918dup
ENST00000680997.1:n.547dup
ENST00000681088.1:c.862dup
ENST00000681608.1:n.148dup
ENST00000681625.1:c.*532dup	ENSP00000505555.1:n.*532dup
ENST00000270301.11:c.3200dup	ENSP00000270301.6:p.Thr1068AspfsTer2
ENST00000401500.6:c.3200dup	ENSP00000384792.1:p.Thr1068AspfsTer2
ENST00000587391.5:c.*2475dup	ENSP00000465525.1:n.*2475dup
NM_001083961.1:c.3200dup	NP_001077430.1:p.Thr1068AspfsTer2
NM_173636.4:c.3200dup	NP_775907.4:p.Thr1068AspfsTer2
XM_005258809.2:c.3089dup	XP_005258866.1:p.Thr1031AspfsTer2
XM_011526837.1:c.3185dup	XP_011525139.1:p.Thr1063AspfsTer2
XM_011526838.1:c.2972-606dup	XP_011525140.1:n.2972-606dup
XM_011526839.1:c.2849dup	XP_011525141.1:p.Thr951AspfsTer2
XM_011526840.1:c.2192dup	XP_011525142.1:p.Thr732AspfsTer2
XM_011526841.1:c.1778dup	XP_011525143.1:p.Thr594AspfsTer2
XM_011526842.1:c.1631dup	XP_011525144.1:p.Thr545AspfsTer2
XM_011526843.1:c.947dup	XP_011525145.1:p.Thr317AspfsTer2
XM_011526844.1:c.947dup	XP_011525146.1:p.Thr317AspfsTer2
XM_011526840.2:c.2192dup	XP_011525142.1:p.Thr732AspfsTer2
XM_011526841.2:c.1778dup	XP_011525143.1:p.Thr594AspfsTer2
XM_011526844.2:c.947dup	XP_011525146.1:p.Thr317AspfsTer2
XM_017026665.1:c.3200dup	XP_016882154.1:p.Thr1068AspfsTer2
NM_001083961.2:c.3200dup MANE Select	NP_001077430.1:p.Thr1068AspfsTer2
NM_173636.5:c.3200dup	NP_775907.4:p.Thr1068AspfsTer2