Canonical Allele Identifier: CA507110939
Community Standard Title: NM_001083961.2(WDR62):c.1941C>T (p.Cys647=)
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36089289C>T , CM000681.2:g.36089289C>T GRCh38
NC_000019.9:g.36580191C>T , CM000681.1:g.36580191C>T GRCh37
NC_000019.8:g.41272031C>T NCBI36
NG_028101.1:g.39409C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001083961.2:c.1941C>T MANE Select NP_001077430.1:p.Cys647=
ENST00000401500.7:c.1941C>T MANE Select ENSP00000384792.1:p.Cys647=
NM_001083961.1:c.1941C>T NP_001077430.1:p.Cys647=
NM_173636.4:c.1941C>T NP_775907.4:p.Cys647=
NM_173636.5:c.1941C>T NP_775907.4:p.Cys647=
ENST00000270301.11:c.1941C>T ENSP00000270301.6:p.Cys647=
ENST00000270301.12:c.1941C>T ENSP00000270301.6:p.Cys647=
ENST00000401500.6:c.1941C>T ENSP00000384792.1:p.Cys647=
ENST00000587391.5:c.*631C>T ENSP00000465525.1:n.*631C>T
ENST00000587391.6:c.*631C>T ENSP00000465525.1:n.*631C>T
ENST00000679489.1:c.259C>T
ENST00000679682.1:c.1926C>T ENSP00000506226.1:p.Cys642=
ENST00000679714.1:c.1935C>T ENSP00000506627.1:p.Cys645=
ENST00000679757.1:c.1590C>T ENSP00000505158.1:p.Cys530=
ENST00000679858.1:c.*738C>T ENSP00000505655.1:n.*738C>T
ENST00000680377.1:c.391C>T
ENST00000680403.1:c.1941C>T ENSP00000505677.1:p.Cys647=
ENST00000680489.1:n.2264C>T
ENST00000680564.1:c.1941C>T ENSP00000505582.1:p.Cys647=
ENST00000680590.1:c.*340C>T ENSP00000505350.1:n.*340C>T
ENST00000680806.1:c.*770C>T ENSP00000506418.1:n.*770C>T
ENST00000680858.1:c.391C>T
ENST00000681302.1:c.391C>T
ENST00000681625.1:c.1926C>T ENSP00000505555.1:p.Cys642=
XM_005258809.2:c.1941C>T XP_005258866.1:p.Cys647=
XM_011526837.1:c.1926C>T XP_011525139.1:p.Cys642=
XM_011526838.1:c.1941C>T XP_011525140.1:p.Cys647=
XM_011526839.1:c.1590C>T XP_011525141.1:p.Cys530=
XM_011526840.1:c.933C>T XP_011525142.1:p.Cys311=
XM_011526840.2:c.933C>T XP_011525142.1:p.Cys311=
XM_011526841.1:c.519C>T XP_011525143.1:p.Cys173=
XM_011526841.2:c.519C>T XP_011525143.1:p.Cys173=
XM_011526842.1:c.372C>T XP_011525144.1:p.Cys124=
XM_017026665.1:c.1941C>T XP_016882154.1:p.Cys647=
XR_001753671.1:n.2032C>T
XR_001753672.1:n.2032C>T