Canonical Allele Identifier: CA2636388238
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793813_17793821del , CM000679.2:g.17793813_17793821del GRCh38
NC_000017.10:g.17697127_17697135del , CM000679.1:g.17697127_17697135del GRCh37
NC_000017.9:g.17637852_17637860del NCBI36
NG_007101.2:g.117341_117349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.865_873del MANE Select ENSP00000323074.4:p.Gln289_Gln291del
ENST00000640861.1:c.799_807del ENSP00000491773.1:p.Gln267_Gln269del
ENST00000353383.5:c.865_873del ENSP00000323074.4:p.Gln289_Gln291del
ENST00000395774.1:c.865_873del ENSP00000379120.1:p.Gln289_Gln291del
NM_030665.3:c.865_873del NP_109590.3:p.Gln289_Gln291del
XM_017024025.1:c.865_873del XP_016879514.1:p.Gln289_Gln291del
XM_017024026.1:c.865_873del XP_016879515.1:p.Gln289_Gln291del
XM_017024027.1:c.865_873del XP_016879516.1:p.Gln289_Gln291del
XM_017024028.2:c.865_873del XP_016879517.1:p.Gln289_Gln291del
NM_030665.4:c.865_873del MANE Select NP_109590.3:p.Gln289_Gln291del