Canonical Allele Identifier: CA625314488
Gene: RAI1 HGNC NCBI

Linked Data

dbSNP Id: rs1263846130

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793797_17793798del , CM000679.2:g.17793797_17793798del GRCh38
NC_000017.10:g.17697111_17697112del , CM000679.1:g.17697111_17697112del GRCh37
NC_000017.9:g.17637836_17637837del NCBI36
NG_007101.2:g.117325_117326del

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.849_850del MANE Select ENSP00000323074.4:p.Gln284AlafsTer?
ENST00000640861.1:c.783_784del ENSP00000491773.1:p.Gln262AlafsTer?
ENST00000353383.5:c.849_850del ENSP00000323074.4:p.Gln284AlafsTer?
ENST00000395774.1:c.849_850del ENSP00000379120.1:p.Gln284AlafsTer?
NM_030665.3:c.849_850del NP_109590.3:p.Gln284AlafsTer?
XM_017024025.1:c.849_850del XP_016879514.1:p.Gln284AlafsTer?
XM_017024026.1:c.849_850del XP_016879515.1:p.Gln284AlafsTer?
XM_017024027.1:c.849_850del XP_016879516.1:p.Gln284AlafsTer?
XM_017024028.2:c.849_850del XP_016879517.1:p.Gln284AlafsTer?
NM_030665.4:c.849_850del MANE Select NP_109590.3:p.Gln284AlafsTer?