Canonical Allele Identifier: CA2250667345
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793796_17793798delinsAGC , CM000679.2:g.17793796_17793798delinsAGC GRCh38
NC_000017.10:g.17697110_17697112delinsAGC , CM000679.1:g.17697110_17697112delinsAGC GRCh37
NC_000017.9:g.17637835_17637837delinsAGC NCBI36
NG_007101.2:g.117324_117326delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.848_850delinsAGC MANE Select ENSP00000323074.4:p.Gln283=
ENST00000640861.1:c.782_784delinsAGC ENSP00000491773.1:p.Gln261=
ENST00000353383.5:c.848_850delinsAGC ENSP00000323074.4:p.Gln283=
ENST00000395774.1:c.848_850delinsAGC ENSP00000379120.1:p.Gln283=
NM_030665.3:c.848_850delinsAGC NP_109590.3:p.Gln283=
XM_017024025.1:c.848_850delinsAGC XP_016879514.1:p.Gln283=
XM_017024026.1:c.848_850delinsAGC XP_016879515.1:p.Gln283=
XM_017024027.1:c.848_850delinsAGC XP_016879516.1:p.Gln283=
XM_017024028.2:c.848_850delinsAGC XP_016879517.1:p.Gln283=
NM_030665.4:c.848_850delinsAGC MANE Select NP_109590.3:p.Gln283=