Canonical Allele Identifier: CA398546281
Gene: RAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793774T>C , CM000679.2:g.17793774T>C GRCh38
NC_000017.10:g.17697088T>C , CM000679.1:g.17697088T>C GRCh37
NC_000017.9:g.17637813T>C NCBI36
NG_007101.2:g.117302T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.826T>C MANE Select ENSP00000323074.4:p.Tyr276His
ENST00000640861.1:c.760T>C ENSP00000491773.1:p.Tyr254His
ENST00000353383.5:c.826T>C ENSP00000323074.4:p.Tyr276His
ENST00000395774.1:c.826T>C ENSP00000379120.1:p.Tyr276His
NM_030665.3:c.826T>C NP_109590.3:p.Tyr276His
XM_017024025.1:c.826T>C XP_016879514.1:p.Tyr276His
XM_017024026.1:c.826T>C XP_016879515.1:p.Tyr276His
XM_017024027.1:c.826T>C XP_016879516.1:p.Tyr276His
XM_017024028.2:c.826T>C XP_016879517.1:p.Tyr276His
NM_030665.4:c.826T>C MANE Select NP_109590.3:p.Tyr276His