Canonical Allele Identifier: CA2250666591
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793664G= , CM000679.2:g.17793664G= GRCh38
NC_000017.10:g.17696978G= , CM000679.1:g.17696978G= GRCh37
NC_000017.9:g.17637703G= NCBI36
NG_007101.2:g.117192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.716G= MANE Select ENSP00000323074.4:p.Cys239=
ENST00000640861.1:c.650G= ENSP00000491773.1:p.Cys217=
ENST00000353383.5:c.716G= ENSP00000323074.4:p.Cys239=
ENST00000395774.1:c.716G= ENSP00000379120.1:p.Cys239=
NM_030665.3:c.716G= NP_109590.3:p.Cys239=
XM_017024025.1:c.716G= XP_016879514.1:p.Cys239=
XM_017024026.1:c.716G= XP_016879515.1:p.Cys239=
XM_017024027.1:c.716G= XP_016879516.1:p.Cys239=
XM_017024028.2:c.716G= XP_016879517.1:p.Cys239=
NM_030665.4:c.716G= MANE Select NP_109590.3:p.Cys239=