Canonical Allele Identifier: CA2250666621
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793672C= , CM000679.2:g.17793672C= GRCh38
NC_000017.10:g.17696986C= , CM000679.1:g.17696986C= GRCh37
NC_000017.9:g.17637711C= NCBI36
NG_007101.2:g.117200C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.724C= MANE Select ENSP00000323074.4:p.Pro242=
ENST00000640861.1:c.658C= ENSP00000491773.1:p.Pro220=
ENST00000353383.5:c.724C= ENSP00000323074.4:p.Pro242=
ENST00000395774.1:c.724C= ENSP00000379120.1:p.Pro242=
NM_030665.3:c.724C= NP_109590.3:p.Pro242=
XM_017024025.1:c.724C= XP_016879514.1:p.Pro242=
XM_017024026.1:c.724C= XP_016879515.1:p.Pro242=
XM_017024027.1:c.724C= XP_016879516.1:p.Pro242=
XM_017024028.2:c.724C= XP_016879517.1:p.Pro242=
NM_030665.4:c.724C= MANE Select NP_109590.3:p.Pro242=