Canonical Allele Identifier: CA2576187124
Gene: RAI1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793613_17793615dup , CM000679.2:g.17793613_17793615dup GRCh38
NC_000017.10:g.17696927_17696929dup , CM000679.1:g.17696927_17696929dup GRCh37
NC_000017.9:g.17637652_17637654dup NCBI36
NG_007101.2:g.117141_117143dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.665_667dup MANE Select ENSP00000323074.4:p.Tyr222_Ser223insTyr
ENST00000640861.1:c.617-17_617-15dup ENSP00000491773.1:n.617-17_617-15dup
ENST00000353383.5:c.665_667dup ENSP00000323074.4:p.Tyr222_Ser223insTyr
ENST00000395774.1:c.665_667dup ENSP00000379120.1:p.Tyr222_Ser223insTyr
NM_030665.3:c.665_667dup NP_109590.3:p.Tyr222_Ser223insTyr
XM_017024025.1:c.665_667dup XP_016879514.1:p.Tyr222_Ser223insTyr
XM_017024026.1:c.665_667dup XP_016879515.1:p.Tyr222_Ser223insTyr
XM_017024027.1:c.665_667dup XP_016879516.1:p.Tyr222_Ser223insTyr
XM_017024028.2:c.665_667dup XP_016879517.1:p.Tyr222_Ser223insTyr
NM_030665.4:c.665_667dup MANE Select NP_109590.3:p.Tyr222_Ser223insTyr
Search 100 bp 5'
Search 100 bp 3'