Canonical Allele Identifier: CA272766
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36091249_36091255dup , CM000681.2:g.36091249_36091255dup GRCh38
NC_000019.9:g.36582151_36582157dup , CM000681.1:g.36582151_36582157dup GRCh37
NC_000019.8:g.41273991_41273997dup NCBI36
NG_028101.1:g.41369_41375dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.2084_2090dup ENSP00000270301.6:p.Ser698LysfsTer6
ENST00000401500.7:c.2084_2090dup MANE Select ENSP00000384792.1:p.Ser698LysfsTer6
ENST00000587391.6:c.*774_*780dup ENSP00000465525.1:n.*774_*780dup
ENST00000679489.1:c.402_408dup
ENST00000679682.1:c.2069_2075dup ENSP00000506226.1:p.Ser693LysfsTer6
ENST00000679714.1:c.2078_2084dup ENSP00000506627.1:p.Ser696LysfsTer6
ENST00000679757.1:c.1733_1739dup ENSP00000505158.1:p.Ser581LysfsTer6
ENST00000679858.1:c.*881_*887dup ENSP00000505655.1:n.*881_*887dup
ENST00000680349.1:n.67_73dup
ENST00000680377.1:c.484+729_484+735dup
ENST00000680403.1:c.2084_2090dup ENSP00000505677.1:p.Ser698LysfsTer6
ENST00000680489.1:n.2407_2413dup
ENST00000680564.1:c.2084_2090dup ENSP00000505582.1:p.Ser698LysfsTer6
ENST00000680590.1:c.*483_*489dup ENSP00000505350.1:n.*483_*489dup
ENST00000680806.1:c.*913_*919dup ENSP00000506418.1:n.*913_*919dup
ENST00000680858.1:c.409-1440_409-1434dup
ENST00000681302.1:c.534_540dup
ENST00000681625.1:c.2069_2075dup ENSP00000505555.1:p.Ser693LysfsTer6
ENST00000270301.11:c.2084_2090dup ENSP00000270301.6:p.Ser698LysfsTer6
ENST00000401500.6:c.2084_2090dup ENSP00000384792.1:p.Ser698LysfsTer6
ENST00000587391.5:c.*774_*780dup ENSP00000465525.1:n.*774_*780dup
NM_001083961.1:c.2084_2090dup NP_001077430.1:p.Ser698LysfsTer6
NM_173636.4:c.2084_2090dup NP_775907.4:p.Ser698LysfsTer6
XM_005258809.2:c.2084_2090dup XP_005258866.1:p.Ser698LysfsTer6
XM_011526837.1:c.2069_2075dup XP_011525139.1:p.Ser693LysfsTer6
XM_011526838.1:c.2084_2090dup XP_011525140.1:p.Ser698LysfsTer6
XM_011526839.1:c.1733_1739dup XP_011525141.1:p.Ser581LysfsTer6
XM_011526840.1:c.1076_1082dup XP_011525142.1:p.Ser362LysfsTer6
XM_011526841.1:c.662_668dup XP_011525143.1:p.Ser224LysfsTer6
XM_011526842.1:c.515_521dup XP_011525144.1:p.Ser175LysfsTer6
XM_011526843.1:c.-44+729_-44+735dup XP_011525145.1:n.-44+729_-44+735dup
XM_011526844.1:c.-106_-100dup XP_011525146.1:n.-106_-100dup
XM_011526840.2:c.1076_1082dup XP_011525142.1:p.Ser362LysfsTer6
XM_011526841.2:c.662_668dup XP_011525143.1:p.Ser224LysfsTer6
XM_011526844.2:c.-106_-100dup XP_011525146.1:n.-106_-100dup
XM_017026665.1:c.2084_2090dup XP_016882154.1:p.Ser698LysfsTer6
XR_001753671.1:n.2175_2181dup
XR_001753672.1:n.2125+729_2125+735dup
NM_001083961.2:c.2084_2090dup MANE Select NP_001077430.1:p.Ser698LysfsTer6
NM_173636.5:c.2084_2090dup NP_775907.4:p.Ser698LysfsTer6