Canonical Allele Identifier: CA2333971348
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102900C= , CM000681.2:g.36102900C= GRCh38
NC_000019.9:g.36593802C= , CM000681.1:g.36593802C= GRCh37
NC_000019.8:g.41285642C= NCBI36
NG_028101.1:g.53020C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3321-48C= ENSP00000270301.6:n.3321-48C=
ENST00000401500.7:c.3336-48C= MANE Select ENSP00000384792.1:n.3336-48C=
ENST00000587391.6:c.*3196-48C= ENSP00000465525.1:n.*3196-48C=
ENST00000679357.1:c.1416-48C=
ENST00000679598.1:c.101-48C=
ENST00000679682.1:c.3321-48C= ENSP00000506226.1:n.3321-48C=
ENST00000679714.1:c.3330-48C= ENSP00000506627.1:n.3330-48C=
ENST00000679757.1:c.2985-48C= ENSP00000505158.1:n.2985-48C=
ENST00000679858.1:c.*2718-48C= ENSP00000505655.1:n.*2718-48C=
ENST00000680211.1:c.-64-48C= ENSP00000506102.1:n.-64-48C=
ENST00000680280.1:n.623-48C=
ENST00000680349.1:n.1904-48C=
ENST00000680403.1:c.3321-48C= ENSP00000505677.1:n.3321-48C=
ENST00000680564.1:c.3087-48C= ENSP00000505582.1:n.3087-48C=
ENST00000680590.1:c.*1716-48C= ENSP00000505350.1:n.*1716-48C=
ENST00000680597.1:c.101-48C=
ENST00000680739.1:c.351-48C=
ENST00000680773.1:n.1837-48C=
ENST00000680806.1:c.*2639-48C= ENSP00000506418.1:n.*2639-48C=
ENST00000680997.1:n.1268-48C=
ENST00000681608.1:n.917C=
ENST00000681625.1:c.*668-48C= ENSP00000505555.1:n.*668-48C=
ENST00000681648.1:n.635-48C=
ENST00000270301.11:c.3321-48C= ENSP00000270301.6:n.3321-48C=
ENST00000401500.6:c.3336-48C= ENSP00000384792.1:n.3336-48C=
ENST00000587391.5:c.*3196-48C= ENSP00000465525.1:n.*3196-48C=
NM_001083961.1:c.3336-48C= NP_001077430.1:n.3336-48C=
NM_173636.4:c.3321-48C= NP_775907.4:n.3321-48C=
XM_005258809.2:c.3225-48C= XP_005258866.1:n.3225-48C=
XM_011526837.1:c.3321-48C= XP_011525139.1:n.3321-48C=
XM_011526838.1:c.3087-48C= XP_011525140.1:n.3087-48C=
XM_011526839.1:c.2985-48C= XP_011525141.1:n.2985-48C=
XM_011526840.1:c.2328-48C= XP_011525142.1:n.2328-48C=
XM_011526841.1:c.1914-48C= XP_011525143.1:n.1914-48C=
XM_011526842.1:c.1767-48C= XP_011525144.1:n.1767-48C=
XM_011526843.1:c.1083-48C= XP_011525145.1:n.1083-48C=
XM_011526844.1:c.1083-48C= XP_011525146.1:n.1083-48C=
XM_011526840.2:c.2328-48C= XP_011525142.1:n.2328-48C=
XM_011526841.2:c.1914-48C= XP_011525143.1:n.1914-48C=
XM_011526844.2:c.1083-48C= XP_011525146.1:n.1083-48C=
XM_017026665.1:c.3336-48C= XP_016882154.1:n.3336-48C=
NM_001083961.2:c.3336-48C= MANE Select NP_001077430.1:n.3336-48C=
NM_173636.5:c.3321-48C= NP_775907.4:n.3321-48C=