Canonical Allele Identifier: CA2695224467
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793778_17793779insGAC , CM000679.2:g.17793778_17793779insGAC GRCh38
NC_000017.10:g.17697092_17697093insGAC , CM000679.1:g.17697092_17697093insGAC GRCh37
NC_000017.9:g.17637817_17637818insGAC NCBI36
NG_007101.2:g.117306_117307insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.830_831insGAC MANE Select ENSP00000323074.4:p.Asp277delinsGluThr
ENST00000640861.1:c.764_765insGAC ENSP00000491773.1:p.Asp255delinsGluThr
ENST00000353383.5:c.830_831insGAC ENSP00000323074.4:p.Asp277delinsGluThr
ENST00000395774.1:c.830_831insGAC ENSP00000379120.1:p.Asp277delinsGluThr
NM_030665.3:c.830_831insGAC NP_109590.3:p.Asp277delinsGluThr
XM_017024025.1:c.830_831insGAC XP_016879514.1:p.Asp277delinsGluThr
XM_017024026.1:c.830_831insGAC XP_016879515.1:p.Asp277delinsGluThr
XM_017024027.1:c.830_831insGAC XP_016879516.1:p.Asp277delinsGluThr
XM_017024028.2:c.830_831insGAC XP_016879517.1:p.Asp277delinsGluThr
NM_030665.4:c.830_831insGAC MANE Select NP_109590.3:p.Asp277delinsGluThr