Canonical Allele Identifier: CA2250666547
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793642G= , CM000679.2:g.17793642G= GRCh38
NC_000017.10:g.17696956G= , CM000679.1:g.17696956G= GRCh37
NC_000017.9:g.17637681G= NCBI36
NG_007101.2:g.117170G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.694G= MANE Select ENSP00000323074.4:p.Gly232=
ENST00000640861.1:c.629G= ENSP00000491773.1:p.Gly210=
ENST00000353383.5:c.694G= ENSP00000323074.4:p.Gly232=
ENST00000395774.1:c.694G= ENSP00000379120.1:p.Gly232=
NM_030665.3:c.694G= NP_109590.3:p.Gly232=
XM_017024025.1:c.694G= XP_016879514.1:p.Gly232=
XM_017024026.1:c.694G= XP_016879515.1:p.Gly232=
XM_017024027.1:c.694G= XP_016879516.1:p.Gly232=
XM_017024028.2:c.694G= XP_016879517.1:p.Gly232=
NM_030665.4:c.694G= MANE Select NP_109590.3:p.Gly232=