Canonical Allele Identifier: CA398546459
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793852A>G , CM000679.2:g.17793852A>G GRCh38
NC_000017.10:g.17697166A>G , CM000679.1:g.17697166A>G GRCh37
NC_000017.9:g.17637891A>G NCBI36
NG_007101.2:g.117380A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.904A>G MANE Select ENSP00000323074.4:p.Thr302Ala
ENST00000640861.1:c.838A>G ENSP00000491773.1:p.Thr280Ala
ENST00000353383.5:c.904A>G ENSP00000323074.4:p.Thr302Ala
ENST00000395774.1:c.904A>G ENSP00000379120.1:p.Thr302Ala
NM_030665.3:c.904A>G NP_109590.3:p.Thr302Ala
XM_017024025.1:c.904A>G XP_016879514.1:p.Thr302Ala
XM_017024026.1:c.904A>G XP_016879515.1:p.Thr302Ala
XM_017024027.1:c.904A>G XP_016879516.1:p.Thr302Ala
XM_017024028.2:c.904A>G XP_016879517.1:p.Thr302Ala
NM_030665.4:c.904A>G MANE Select NP_109590.3:p.Thr302Ala