Canonical Allele Identifier: CA2250666517
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793626C= , CM000679.2:g.17793626C= GRCh38
NC_000017.10:g.17696940C= , CM000679.1:g.17696940C= GRCh37
NC_000017.9:g.17637665C= NCBI36
NG_007101.2:g.117154C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.678C= MANE Select ENSP00000323074.4:p.Val226=
ENST00000640861.1:c.617-4C= ENSP00000491773.1:n.617-4C=
ENST00000353383.5:c.678C= ENSP00000323074.4:p.Val226=
ENST00000395774.1:c.678C= ENSP00000379120.1:p.Val226=
NM_030665.3:c.678C= NP_109590.3:p.Val226=
XM_017024025.1:c.678C= XP_016879514.1:p.Val226=
XM_017024026.1:c.678C= XP_016879515.1:p.Val226=
XM_017024027.1:c.678C= XP_016879516.1:p.Val226=
XM_017024028.2:c.678C= XP_016879517.1:p.Val226=
NM_030665.4:c.678C= MANE Select NP_109590.3:p.Val226=