Canonical Allele Identifier: CA2250667231
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793787_17793791delinsAGCAG , CM000679.2:g.17793787_17793791delinsAGCAG GRCh38
NC_000017.10:g.17697101_17697105delinsAGCAG , CM000679.1:g.17697101_17697105delinsAGCAG GRCh37
NC_000017.9:g.17637826_17637830delinsAGCAG NCBI36
NG_007101.2:g.117315_117319delinsAGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.839_843delinsAGCAG MANE Select ENSP00000323074.4:p.Gln280=
ENST00000640861.1:c.773_777delinsAGCAG ENSP00000491773.1:p.Gln258=
ENST00000353383.5:c.839_843delinsAGCAG ENSP00000323074.4:p.Gln280=
ENST00000395774.1:c.839_843delinsAGCAG ENSP00000379120.1:p.Gln280=
NM_030665.3:c.839_843delinsAGCAG NP_109590.3:p.Gln280=
XM_017024025.1:c.839_843delinsAGCAG XP_016879514.1:p.Gln280=
XM_017024026.1:c.839_843delinsAGCAG XP_016879515.1:p.Gln280=
XM_017024027.1:c.839_843delinsAGCAG XP_016879516.1:p.Gln280=
XM_017024028.2:c.839_843delinsAGCAG XP_016879517.1:p.Gln280=
NM_030665.4:c.839_843delinsAGCAG MANE Select NP_109590.3:p.Gln280=