Canonical Allele Identifier: CA398546283

Gene: RAI1

Linked Data

• ClinVar Variation Id: 2320104
• ClinVar RCV Id: RCV002919847
• dbSNP Id: rs146690371
• MyVariant Identifiers: chr17:g.17697089A>T (hg19) ; chr17:g.17793775A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793775A>T , CM000679.2:g.17793775A>T	GRCh38
NC_000017.10:g.17697089A>T , CM000679.1:g.17697089A>T	GRCh37
NC_000017.9:g.17637814A>T	NCBI36
NG_007101.2:g.117303A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.827A>T MANE Select	ENSP00000323074.4:p.Tyr276Phe
ENST00000640861.1:c.761A>T	ENSP00000491773.1:p.Tyr254Phe
ENST00000353383.5:c.827A>T	ENSP00000323074.4:p.Tyr276Phe
ENST00000395774.1:c.827A>T	ENSP00000379120.1:p.Tyr276Phe
NM_030665.3:c.827A>T	NP_109590.3:p.Tyr276Phe
XM_017024025.1:c.827A>T	XP_016879514.1:p.Tyr276Phe
XM_017024026.1:c.827A>T	XP_016879515.1:p.Tyr276Phe
XM_017024027.1:c.827A>T	XP_016879516.1:p.Tyr276Phe
XM_017024028.2:c.827A>T	XP_016879517.1:p.Tyr276Phe
NM_030665.4:c.827A>T MANE Select	NP_109590.3:p.Tyr276Phe