Canonical Allele Identifier: CA288367406
Gene: RAI1 HGNC NCBI

Linked Data

dbSNP Id: rs372058626

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793817dup , CM000679.2:g.17793817dup GRCh38
NC_000017.10:g.17697131dup , CM000679.1:g.17697131dup GRCh37
NC_000017.9:g.17637856dup NCBI36
NG_007101.2:g.117345dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.869dup MANE Select ENSP00000323074.4:p.Gln291AlafsTer?
ENST00000640861.1:c.803dup ENSP00000491773.1:p.Gln269AlafsTer?
ENST00000353383.5:c.869dup ENSP00000323074.4:p.Gln291AlafsTer?
ENST00000395774.1:c.869dup ENSP00000379120.1:p.Gln291AlafsTer?
NM_030665.3:c.869dup NP_109590.3:p.Gln291AlafsTer?
XM_017024025.1:c.869dup XP_016879514.1:p.Gln291AlafsTer?
XM_017024026.1:c.869dup XP_016879515.1:p.Gln291AlafsTer?
XM_017024027.1:c.869dup XP_016879516.1:p.Gln291AlafsTer?
XM_017024028.2:c.869dup XP_016879517.1:p.Gln291AlafsTer?
NM_030665.4:c.869dup MANE Select NP_109590.3:p.Gln291AlafsTer?