Canonical Allele Identifier: CA645589910
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793785del , CM000679.2:g.17793785del GRCh38
NC_000017.10:g.17697099del , CM000679.1:g.17697099del GRCh37
NC_000017.9:g.17637824del NCBI36
NG_007101.2:g.117313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.837del MANE Select ENSP00000323074.4:p.Gln279HisfsTer?
ENST00000640861.1:c.771del ENSP00000491773.1:p.Gln257HisfsTer?
ENST00000353383.5:c.837del ENSP00000323074.4:p.Gln279HisfsTer?
ENST00000395774.1:c.837del ENSP00000379120.1:p.Gln279HisfsTer?
NM_030665.3:c.837del NP_109590.3:p.Gln279HisfsTer?
XM_017024025.1:c.837del XP_016879514.1:p.Gln279HisfsTer?
XM_017024026.1:c.837del XP_016879515.1:p.Gln279HisfsTer?
XM_017024027.1:c.837del XP_016879516.1:p.Gln279HisfsTer?
XM_017024028.2:c.837del XP_016879517.1:p.Gln279HisfsTer?
NM_030665.4:c.837del MANE Select NP_109590.3:p.Gln279HisfsTer?