Canonical Allele Identifier: CA2695224465
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793466_17793467insG , CM000679.2:g.17793466_17793467insG GRCh38
NC_000017.10:g.17696780_17696781insG , CM000679.1:g.17696780_17696781insG GRCh37
NC_000017.9:g.17637505_17637506insG NCBI36
NG_007101.2:g.116994_116995insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.518_519insG MANE Select ENSP00000323074.4:p.Gln174ProfsTer?
ENST00000640861.1:c.518_519insG ENSP00000491773.1:p.Gln174ProfsTer?
ENST00000353383.5:c.518_519insG ENSP00000323074.4:p.Gln174ProfsTer?
ENST00000395774.1:c.518_519insG ENSP00000379120.1:p.Gln174ProfsTer?
NM_030665.3:c.518_519insG NP_109590.3:p.Gln174ProfsTer?
XM_017024025.1:c.518_519insG XP_016879514.1:p.Gln174ProfsTer?
XM_017024026.1:c.518_519insG XP_016879515.1:p.Gln174ProfsTer?
XM_017024027.1:c.518_519insG XP_016879516.1:p.Gln174ProfsTer?
XM_017024028.2:c.518_519insG XP_016879517.1:p.Gln174ProfsTer?
NM_030665.4:c.518_519insG MANE Select NP_109590.3:p.Gln174ProfsTer?