Canonical Allele Identifier: CA2333971387
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102970_36102971delinsCG , CM000681.2:g.36102970_36102971delinsCG GRCh38
NC_000019.9:g.36593872_36593873delinsCG , CM000681.1:g.36593872_36593873delinsCG GRCh37
NC_000019.8:g.41285712_41285713delinsCG NCBI36
NG_028101.1:g.53090_53091delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3343_3344delinsCG ENSP00000270301.6:p.Arg1115=
ENST00000401500.7:c.3358_3359delinsCG MANE Select ENSP00000384792.1:p.Arg1120=
ENST00000587391.6:c.*3218_*3219delinsCG ENSP00000465525.1:n.*3218_*3219delinsCG
ENST00000679357.1:c.1438_1439delinsCG
ENST00000679598.1:c.123_124delinsCG
ENST00000679682.1:c.3343_3344delinsCG ENSP00000506226.1:p.Arg1115=
ENST00000679714.1:c.3352_3353delinsCG ENSP00000506627.1:p.Arg1118=
ENST00000679757.1:c.3007_3008delinsCG ENSP00000505158.1:p.Arg1003=
ENST00000679858.1:c.*2740_*2741delinsCG ENSP00000505655.1:n.*2740_*2741delinsCG
ENST00000680211.1:c.-42_-41delinsCG ENSP00000506102.1:n.-42_-41delinsCG
ENST00000680280.1:n.645_646delinsCG
ENST00000680349.1:n.1926_1927delinsCG
ENST00000680403.1:c.3343_3344delinsCG ENSP00000505677.1:p.Arg1115=
ENST00000680564.1:c.3109_3110delinsCG ENSP00000505582.1:p.Arg1037=
ENST00000680590.1:c.*1738_*1739delinsCG ENSP00000505350.1:n.*1738_*1739delinsCG
ENST00000680597.1:c.123_124delinsCG
ENST00000680739.1:c.373_374delinsCG
ENST00000680773.1:n.1859_1860delinsCG
ENST00000680806.1:c.*2661_*2662delinsCG ENSP00000506418.1:n.*2661_*2662delinsCG
ENST00000680997.1:n.1290_1291delinsCG
ENST00000681608.1:n.987_988delinsCG
ENST00000681625.1:c.*690_*691delinsCG ENSP00000505555.1:n.*690_*691delinsCG
ENST00000681648.1:n.657_658delinsCG
ENST00000270301.11:c.3343_3344delinsCG ENSP00000270301.6:p.Arg1115=
ENST00000401500.6:c.3358_3359delinsCG ENSP00000384792.1:p.Arg1120=
ENST00000587391.5:c.*3218_*3219delinsCG ENSP00000465525.1:n.*3218_*3219delinsCG
NM_001083961.1:c.3358_3359delinsCG NP_001077430.1:p.Arg1120=
NM_173636.4:c.3343_3344delinsCG NP_775907.4:p.Arg1115=
XM_005258809.2:c.3247_3248delinsCG XP_005258866.1:p.Arg1083=
XM_011526837.1:c.3343_3344delinsCG XP_011525139.1:p.Arg1115=
XM_011526838.1:c.3109_3110delinsCG XP_011525140.1:p.Arg1037=
XM_011526839.1:c.3007_3008delinsCG XP_011525141.1:p.Arg1003=
XM_011526840.1:c.2350_2351delinsCG XP_011525142.1:p.Arg784=
XM_011526841.1:c.1936_1937delinsCG XP_011525143.1:p.Arg646=
XM_011526842.1:c.1789_1790delinsCG XP_011525144.1:p.Arg597=
XM_011526843.1:c.1105_1106delinsCG XP_011525145.1:p.Arg369=
XM_011526844.1:c.1105_1106delinsCG XP_011525146.1:p.Arg369=
XM_011526840.2:c.2350_2351delinsCG XP_011525142.1:p.Arg784=
XM_011526841.2:c.1936_1937delinsCG XP_011525143.1:p.Arg646=
XM_011526844.2:c.1105_1106delinsCG XP_011525146.1:p.Arg369=
XM_017026665.1:c.3358_3359delinsCG XP_016882154.1:p.Arg1120=
NM_001083961.2:c.3358_3359delinsCG MANE Select NP_001077430.1:p.Arg1120=
NM_173636.5:c.3343_3344delinsCG NP_775907.4:p.Arg1115=