Canonical Allele Identifier: CA2250666432
Gene: RAI1 HGNC NCBI

Linked Data

dbSNP Id: rs2032106589

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793609_17793623dup , CM000679.2:g.17793609_17793623dup GRCh38
NC_000017.10:g.17696923_17696937dup , CM000679.1:g.17696923_17696937dup GRCh37
NC_000017.9:g.17637648_17637662dup NCBI36
NG_007101.2:g.117137_117151dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.661_675dup MANE Select ENSP00000323074.4:p.Ser225_Val226insThrTyrSerSerSer
ENST00000640861.1:c.617-21_617-7dup ENSP00000491773.1:n.617-21_617-7dup
ENST00000353383.5:c.661_675dup ENSP00000323074.4:p.Ser225_Val226insThrTyrSerSerSer
ENST00000395774.1:c.661_675dup ENSP00000379120.1:p.Ser225_Val226insThrTyrSerSerSer
NM_030665.3:c.661_675dup NP_109590.3:p.Ser225_Val226insThrTyrSerSerSer
XM_017024025.1:c.661_675dup XP_016879514.1:p.Ser225_Val226insThrTyrSerSerSer
XM_017024026.1:c.661_675dup XP_016879515.1:p.Ser225_Val226insThrTyrSerSerSer
XM_017024027.1:c.661_675dup XP_016879516.1:p.Ser225_Val226insThrTyrSerSerSer
XM_017024028.2:c.661_675dup XP_016879517.1:p.Ser225_Val226insThrTyrSerSerSer
NM_030665.4:c.661_675dup MANE Select NP_109590.3:p.Ser225_Val226insThrTyrSerSerSer