Canonical Allele Identifier: CA2497029353
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793779_17793782delinsCCAG , CM000679.2:g.17793779_17793782delinsCCAG GRCh38
NC_000017.10:g.17697093_17697096delinsCCAG , CM000679.1:g.17697093_17697096delinsCCAG GRCh37
NC_000017.9:g.17637818_17637821delinsCCAG NCBI36
NG_007101.2:g.117307_117310delinsCCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.831_834delinsCCAG MANE Select ENSP00000323074.4:p.Asp277=
ENST00000640861.1:c.765_768delinsCCAG ENSP00000491773.1:p.Asp255=
ENST00000353383.5:c.831_834delinsCCAG ENSP00000323074.4:p.Asp277=
ENST00000395774.1:c.831_834delinsCCAG ENSP00000379120.1:p.Asp277=
NM_030665.3:c.831_834delinsCCAG NP_109590.3:p.Asp277=
XM_017024025.1:c.831_834delinsCCAG XP_016879514.1:p.Asp277=
XM_017024026.1:c.831_834delinsCCAG XP_016879515.1:p.Asp277=
XM_017024027.1:c.831_834delinsCCAG XP_016879516.1:p.Asp277=
XM_017024028.2:c.831_834delinsCCAG XP_016879517.1:p.Asp277=
NM_030665.4:c.831_834delinsCCAG MANE Select NP_109590.3:p.Asp277=