Canonical Allele Identifier: CA370067304
Community Standard Title: NM_198285.3(WDR86):c.913G>C (p.Gly305Arg)
Gene: WDR86 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151381931C>G , CM000669.2:g.151381931C>G GRCh38
NC_000007.13:g.151079017C>G , CM000669.1:g.151079017C>G GRCh37
NC_000007.12:g.150709950C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_198285.3:c.913G>C MANE Select NP_938026.2:p.Gly305Arg
ENST00000334493.11:c.913G>C MANE Select ENSP00000335522.7:p.Gly305Arg
NM_001284260.1:c.977G>C NP_001271189.1:p.Trp326Ser
NM_001284260.2:c.977G>C NP_001271189.1:p.Trp326Ser
NM_001284261.1:c.393G>C NP_001271190.1:p.Leu131=
NM_001284261.2:c.393G>C NP_001271190.1:p.Leu131=
NM_001284262.1:c.529G>C NP_001271191.1:p.Gly177Arg
NM_001284262.2:c.529G>C NP_001271191.1:p.Gly177Arg
NM_198285.2:c.913G>C NP_938026.2:p.Gly305Arg
ENST00000334493.10:c.913G>C ENSP00000335522.6:p.Gly305Arg
ENST00000463000.1:n.143-4784G>C
ENST00000469830.2:c.977G>C ENSP00000419162.2:p.Trp326Ser
ENST00000477459.5:c.393G>C ENSP00000417512.1:p.Leu131=
ENST00000621812.2:c.529G>C ENSP00000482209.1:p.Gly177Arg
ENST00000628331.1:c.393G>C ENSP00000486705.1:p.Leu131=
XM_005249989.3:c.777G>C XP_005250046.1:p.Leu259=
XM_005249989.4:c.777G>C XP_005250046.1:p.Leu259=
XM_005249990.3:c.913G>C XP_005250047.1:p.Gly305Arg
XM_005249990.5:c.913G>C XP_005250047.1:p.Gly305Arg
XM_011516144.1:c.977G>C XP_011514446.1:p.Trp326Ser
XM_011516144.3:c.977G>C XP_011514446.1:p.Trp326Ser
XM_011516145.1:c.977G>C XP_011514447.1:p.Trp326Ser
XM_011516145.3:c.977G>C XP_011514447.1:p.Trp326Ser
XM_011516146.1:c.913G>C XP_011514448.1:p.Gly305Arg
XM_011516146.3:c.913G>C XP_011514448.1:p.Gly305Arg
XM_011516147.1:c.777G>C XP_011514449.1:p.Leu259=
XM_011516147.3:c.777G>C XP_011514449.1:p.Leu259=
XM_011516148.1:c.593G>C XP_011514450.1:p.Trp198Ser
XM_011516149.1:c.593G>C XP_011514451.1:p.Trp198Ser
XM_011516150.1:c.593G>C XP_011514452.1:p.Trp198Ser
XM_011516151.1:c.777G>C XP_011514453.1:p.Leu259=
XM_011516151.3:c.777G>C XP_011514453.1:p.Leu259=
XM_011516153.1:c.529G>C XP_011514455.1:p.Gly177Arg
XM_011516154.1:c.529G>C XP_011514456.1:p.Gly177Arg
XM_011516155.1:c.412G>C XP_011514457.1:p.Gly138Arg