Canonical Allele Identifier: CA2573105828
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793822dup , CM000679.2:g.17793822dup GRCh38
NC_000017.10:g.17697136dup , CM000679.1:g.17697136dup GRCh37
NC_000017.9:g.17637861dup NCBI36
NG_007101.2:g.117350dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.874dup MANE Select ENSP00000323074.4:p.Ala292GlyfsTer?
ENST00000640861.1:c.808dup ENSP00000491773.1:p.Ala270GlyfsTer?
ENST00000353383.5:c.874dup ENSP00000323074.4:p.Ala292GlyfsTer?
ENST00000395774.1:c.874dup ENSP00000379120.1:p.Ala292GlyfsTer?
NM_030665.3:c.874dup NP_109590.3:p.Ala292GlyfsTer?
XM_017024025.1:c.874dup XP_016879514.1:p.Ala292GlyfsTer?
XM_017024026.1:c.874dup XP_016879515.1:p.Ala292GlyfsTer?
XM_017024027.1:c.874dup XP_016879516.1:p.Ala292GlyfsTer?
XM_017024028.2:c.874dup XP_016879517.1:p.Ala292GlyfsTer?
NM_030665.4:c.874dup MANE Select NP_109590.3:p.Ala292GlyfsTer?