Canonical Allele Identifier: CA2636388239
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793820_17793821insGCAGCAGCAGCAGC , CM000679.2:g.17793820_17793821insGCAGCAGCAGCAGC GRCh38
NC_000017.10:g.17697134_17697135insGCAGCAGCAGCAGC , CM000679.1:g.17697134_17697135insGCAGCAGCAGCAGC GRCh37
NC_000017.9:g.17637859_17637860insGCAGCAGCAGCAGC NCBI36
NG_007101.2:g.117348_117349insGCAGCAGCAGCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.872_873insGCAGCAGCAGCAGC MANE Select ENSP00000323074.4:p.Ala292GlnfsTer?
ENST00000640861.1:c.806_807insGCAGCAGCAGCAGC ENSP00000491773.1:p.Ala270GlnfsTer?
ENST00000353383.5:c.872_873insGCAGCAGCAGCAGC ENSP00000323074.4:p.Ala292GlnfsTer?
ENST00000395774.1:c.872_873insGCAGCAGCAGCAGC ENSP00000379120.1:p.Ala292GlnfsTer?
NM_030665.3:c.872_873insGCAGCAGCAGCAGC NP_109590.3:p.Ala292GlnfsTer?
XM_017024025.1:c.872_873insGCAGCAGCAGCAGC XP_016879514.1:p.Ala292GlnfsTer?
XM_017024026.1:c.872_873insGCAGCAGCAGCAGC XP_016879515.1:p.Ala292GlnfsTer?
XM_017024027.1:c.872_873insGCAGCAGCAGCAGC XP_016879516.1:p.Ala292GlnfsTer?
XM_017024028.2:c.872_873insGCAGCAGCAGCAGC XP_016879517.1:p.Ala292GlnfsTer?
NM_030665.4:c.872_873insGCAGCAGCAGCAGC MANE Select NP_109590.3:p.Ala292GlnfsTer?