Canonical Allele Identifier: CA398545721

Gene: RAI1

Linked Data

• ClinVar Variation Id: 1311149
• ClinVar RCV Id: RCV001758658
• dbSNP Id: rs2143001624
• MyVariant Identifiers: chr17:g.17696821A>G (hg19) ; chr17:g.17793507A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793507A>G , CM000679.2:g.17793507A>G	GRCh38
NC_000017.10:g.17696821A>G , CM000679.1:g.17696821A>G	GRCh37
NC_000017.9:g.17637546A>G	NCBI36
NG_007101.2:g.117035A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.559A>G MANE Select	ENSP00000323074.4:p.Lys187Glu
ENST00000640861.1:c.559A>G	ENSP00000491773.1:p.Lys187Glu
ENST00000353383.5:c.559A>G	ENSP00000323074.4:p.Lys187Glu
ENST00000395774.1:c.559A>G	ENSP00000379120.1:p.Lys187Glu
NM_030665.3:c.559A>G	NP_109590.3:p.Lys187Glu
XM_017024025.1:c.559A>G	XP_016879514.1:p.Lys187Glu
XM_017024026.1:c.559A>G	XP_016879515.1:p.Lys187Glu
XM_017024027.1:c.559A>G	XP_016879516.1:p.Lys187Glu
XM_017024028.2:c.559A>G	XP_016879517.1:p.Lys187Glu
NM_030665.4:c.559A>G MANE Select	NP_109590.3:p.Lys187Glu