Canonical Allele Identifier: CA2333970967

Gene: WDR62

Linked Data

• dbSNP Id: rs1973394904

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102150_36102151dup , CM000681.2:g.36102150_36102151dup	GRCh38
NC_000019.9:g.36593052_36593053dup , CM000681.1:g.36593052_36593053dup	GRCh37
NC_000019.8:g.41284892_41284893dup	NCBI36
NG_028101.1:g.52270_52271dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3219_3220dup	ENSP00000270301.6:p.Ala1074GlufsTer20
ENST00000401500.7:c.3219_3220dup MANE Select	ENSP00000384792.1:p.Leu1075SerfsTer24
ENST00000587391.6:c.*2494_*2495dup	ENSP00000465525.1:n.*2494_*2495dup
ENST00000679357.1:c.1009_1010dup
ENST00000679682.1:c.3204_3205dup	ENSP00000506226.1:p.Leu1070SerfsTer24
ENST00000679714.1:c.3213_3214dup	ENSP00000506627.1:p.Leu1073SerfsTer24
ENST00000679757.1:c.2868_2869dup	ENSP00000505158.1:p.Leu958SerfsTer24
ENST00000679858.1:c.*2601_*2602dup	ENSP00000505655.1:n.*2601_*2602dup
ENST00000680211.1:c.-181_-180dup	ENSP00000506102.1:n.-181_-180dup
ENST00000680349.1:n.1202_1203dup
ENST00000680403.1:c.3219_3220dup	ENSP00000505677.1:p.Ala1074GlufsTer20
ENST00000680564.1:c.2972-587_2972-586dup	ENSP00000505582.1:n.2972-587_2972-586dup
ENST00000680590.1:c.*1614_*1615dup	ENSP00000505350.1:n.*1614_*1615dup
ENST00000680739.1:c.137_138dup
ENST00000680773.1:n.1135_1136dup
ENST00000680806.1:c.*1937_*1938dup	ENSP00000506418.1:n.*1937_*1938dup
ENST00000680997.1:n.566_567dup
ENST00000681608.1:n.167_168dup
ENST00000681625.1:c.*551_*552dup	ENSP00000505555.1:n.*551_*552dup
ENST00000270301.11:c.3219_3220dup	ENSP00000270301.6:p.Ala1074GlufsTer20
ENST00000401500.6:c.3219_3220dup	ENSP00000384792.1:p.Leu1075SerfsTer24
ENST00000587391.5:c.*2494_*2495dup	ENSP00000465525.1:n.*2494_*2495dup
NM_001083961.1:c.3219_3220dup	NP_001077430.1:p.Leu1075SerfsTer24
NM_173636.4:c.3219_3220dup	NP_775907.4:p.Ala1074GlufsTer20
XM_005258809.2:c.3108_3109dup	XP_005258866.1:p.Leu1038SerfsTer24
XM_011526837.1:c.3204_3205dup	XP_011525139.1:p.Leu1070SerfsTer24
XM_011526838.1:c.2972-587_2972-586dup	XP_011525140.1:n.2972-587_2972-586dup
XM_011526839.1:c.2868_2869dup	XP_011525141.1:p.Leu958SerfsTer24
XM_011526840.1:c.2211_2212dup	XP_011525142.1:p.Leu739SerfsTer24
XM_011526841.1:c.1797_1798dup	XP_011525143.1:p.Leu601SerfsTer24
XM_011526842.1:c.1650_1651dup	XP_011525144.1:p.Leu552SerfsTer24
XM_011526843.1:c.966_967dup	XP_011525145.1:p.Leu324SerfsTer24
XM_011526844.1:c.966_967dup	XP_011525146.1:p.Leu324SerfsTer24
XM_011526840.2:c.2211_2212dup	XP_011525142.1:p.Leu739SerfsTer24
XM_011526841.2:c.1797_1798dup	XP_011525143.1:p.Leu601SerfsTer24
XM_011526844.2:c.966_967dup	XP_011525146.1:p.Leu324SerfsTer24
XM_017026665.1:c.3219_3220dup	XP_016882154.1:p.Leu1075SerfsTer24
NM_001083961.2:c.3219_3220dup MANE Select	NP_001077430.1:p.Leu1075SerfsTer24
NM_173636.5:c.3219_3220dup	NP_775907.4:p.Ala1074GlufsTer20