Canonical Allele Identifier: CA2250666038
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793463A= , CM000679.2:g.17793463A= GRCh38
NC_000017.10:g.17696777A= , CM000679.1:g.17696777A= GRCh37
NC_000017.9:g.17637502A= NCBI36
NG_007101.2:g.116991A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.515A= MANE Select ENSP00000323074.4:p.His172=
ENST00000640861.1:c.515A= ENSP00000491773.1:p.His172=
ENST00000353383.5:c.515A= ENSP00000323074.4:p.His172=
ENST00000395774.1:c.515A= ENSP00000379120.1:p.His172=
NM_030665.3:c.515A= NP_109590.3:p.His172=
XM_017024025.1:c.515A= XP_016879514.1:p.His172=
XM_017024026.1:c.515A= XP_016879515.1:p.His172=
XM_017024027.1:c.515A= XP_016879516.1:p.His172=
XM_017024028.2:c.515A= XP_016879517.1:p.His172=
NM_030665.4:c.515A= MANE Select NP_109590.3:p.His172=