Canonical Allele Identifier: CA2250667473
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793818_17793821delinsGCAA , CM000679.2:g.17793818_17793821delinsGCAA GRCh38
NC_000017.10:g.17697132_17697135delinsGCAA , CM000679.1:g.17697132_17697135delinsGCAA GRCh37
NC_000017.9:g.17637857_17637860delinsGCAA NCBI36
NG_007101.2:g.117346_117349delinsGCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.870_873delinsGCAA MANE Select ENSP00000323074.4:p.Gln290=
ENST00000640861.1:c.804_807delinsGCAA ENSP00000491773.1:p.Gln268=
ENST00000353383.5:c.870_873delinsGCAA ENSP00000323074.4:p.Gln290=
ENST00000395774.1:c.870_873delinsGCAA ENSP00000379120.1:p.Gln290=
NM_030665.3:c.870_873delinsGCAA NP_109590.3:p.Gln290=
XM_017024025.1:c.870_873delinsGCAA XP_016879514.1:p.Gln290=
XM_017024026.1:c.870_873delinsGCAA XP_016879515.1:p.Gln290=
XM_017024027.1:c.870_873delinsGCAA XP_016879516.1:p.Gln290=
XM_017024028.2:c.870_873delinsGCAA XP_016879517.1:p.Gln290=
NM_030665.4:c.870_873delinsGCAA MANE Select NP_109590.3:p.Gln290=